首页 > 最新文献

International Journal of Surgery Case Reports最新文献

英文 中文
Colonic actinomycosis masquerading a cancer resulting complete bowel obstruction-a case report 伪装成癌症导致完全性肠梗阻的结肠放线菌病--病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-04 DOI: 10.1016/j.ijscr.2024.110563
Lilamani Rajthala , Santosh Sirpaili , Krishna Mohan Adhikari

Introduction

Colonic actinomycosis is an uncommon chronic infection associated with granulomatous inflammation resulting multiple abscesses and sinuses. Common modes of presentation include weight loss, malaise, abdominal pain, and abdominal mass, which might mimic neoplasia.

Case presentation

A 60-year-old female presented with painful lump in right iliac fossa (RIF) for 3 weeks and acute complete bowel obstruction for 3 days. Examination revealed hard, irregular and fixed lump in the RIF. Ultrasonography of abdomen and pelvis showed ileocecal mass while contract enhanced computed tomography (CECT) suggested carcinoma transverse colon with mesenteric metastasis. The patient underwent emergency exploratory laparotomy and right extended hemicolectomy for densely adherent mass incorporating distal ileum, cecum, ascending and proximal transverse colon with adjacent mesenteries. However, histopathological examination revealed colonic actinomycosis. The patient was commenced on intravenous penicillin G followed by oral amoxicillin.

Clinical discussion

Colonic actinomycosis is a rare infection presenting with pain abdomen, change in bowel habit, and rarely, abdominal mass. Preoperative diagnosis is difficult due to lack of pathognomonic clinical, laboratory and radiological findings. Differentiation from other diseases such as appendicitis, diverticulitis, colon carcinoma, Crohn's disease, and ulcerative colitis is challenging. Diagnosis is confirmed histologically by presence of Periodic acid-Schiff (PAS) and Grocott- positive sulphur granules with filaments. Newer molecular diagnoses are under study. Medical therapy is main line of treatment, most effectively with parenteral and oral beta lactams.

Conclusion

Actinomycosis may present with aggressive invasion and infiltration of adjacent organs, mesentery, and abdominal wall mimicking malignancy. Acute presentation with bowel obstruction would mandate surgical intervention.
简介结肠放线菌病是一种不常见的慢性感染,伴有肉芽肿性炎症,导致多发性脓肿和窦道。常见的表现形式包括体重减轻、乏力、腹痛和腹部肿块,可能与肿瘤相似:一名 60 岁女性因右髂窝(RIF)肿块疼痛 3 周和急性完全性肠梗阻 3 天就诊。检查发现右髂窝肿块坚硬、不规则且固定。腹部和盆腔超声检查显示回盲部肿块,而收缩增强计算机断层扫描(CECT)显示横结肠癌伴肠系膜转移。患者接受了急诊剖腹探查术和右侧扩大半结肠切除术,切除了包括回肠远端、盲肠、升结肠和横结肠近端以及邻近肠系膜的密集粘连肿块。然而,组织病理学检查发现结肠放线菌病。患者开始静脉注射青霉素 G,随后口服阿莫西林:结肠放线菌病是一种罕见的感染,表现为腹部疼痛、排便习惯改变,很少出现腹部肿块。由于缺乏病理临床、实验室和放射学检查结果,术前诊断十分困难。与阑尾炎、憩室炎、结肠癌、克罗恩病和溃疡性结肠炎等其他疾病的鉴别也很困难。在组织学上,如果出现带丝的周期性酸-希夫(PAS)和格罗戈特(Grocott)阳性硫颗粒,即可确诊。目前正在研究新的分子诊断方法。药物治疗是主要的治疗方法,使用肠外和口服β内酰胺类药物最为有效:结论:放线菌病可能会出现侵犯和浸润邻近器官、肠系膜和腹壁的症状,与恶性肿瘤相似。急性发作并伴有肠梗阻时,必须进行手术治疗。
{"title":"Colonic actinomycosis masquerading a cancer resulting complete bowel obstruction-a case report","authors":"Lilamani Rajthala ,&nbsp;Santosh Sirpaili ,&nbsp;Krishna Mohan Adhikari","doi":"10.1016/j.ijscr.2024.110563","DOIUrl":"10.1016/j.ijscr.2024.110563","url":null,"abstract":"<div><h3>Introduction</h3><div>Colonic actinomycosis is an uncommon chronic infection associated with granulomatous inflammation resulting multiple abscesses and sinuses. Common modes of presentation include weight loss, malaise, abdominal pain, and abdominal mass, which might mimic neoplasia.</div></div><div><h3>Case presentation</h3><div>A 60-year-old female presented with painful lump in right iliac fossa (RIF) for 3 weeks and acute complete bowel obstruction for 3 days. Examination revealed hard, irregular and fixed lump in the RIF. Ultrasonography of abdomen and pelvis showed ileocecal mass while contract enhanced computed tomography (CECT) suggested carcinoma transverse colon with mesenteric metastasis. The patient underwent emergency exploratory laparotomy and right extended hemicolectomy for densely adherent mass incorporating distal ileum, cecum, ascending and proximal transverse colon with adjacent mesenteries. However, histopathological examination revealed colonic actinomycosis. The patient was commenced on intravenous penicillin G followed by oral amoxicillin.</div></div><div><h3>Clinical discussion</h3><div>Colonic actinomycosis is a rare infection presenting with pain abdomen, change in bowel habit, and rarely, abdominal mass. Preoperative diagnosis is difficult due to lack of pathognomonic clinical, laboratory and radiological findings. Differentiation from other diseases such as appendicitis, diverticulitis, colon carcinoma, Crohn's disease, and ulcerative colitis is challenging. Diagnosis is confirmed histologically by presence of Periodic acid-Schiff (PAS) and Grocott- positive sulphur granules with filaments. Newer molecular diagnoses are under study. Medical therapy is main line of treatment, most effectively with parenteral and oral beta lactams.</div></div><div><h3>Conclusion</h3><div>Actinomycosis may present with aggressive invasion and infiltration of adjacent organs, mesentery, and abdominal wall mimicking malignancy. Acute presentation with bowel obstruction would mandate surgical intervention.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110563"},"PeriodicalIF":0.6,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142630436","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cure of urethro-rectal fistula secondary to a road traffic accident by perineal approach with gracilis flap interposition: A case report 通过会阴入路与腓骨瓣插入术治愈道路交通事故继发的尿道直肠瘘:病例报告
IF 0.6 Q4 SURGERY Pub Date : 2024-11-04 DOI: 10.1016/j.ijscr.2024.110564
M.L. Foba , S.M.A. Fall , F.J. Tchoungui Ritz , B. Sine , M. Beye , A.A. Sankalé

Introduction

A urethro-rectal fistula is an abnormal communication between the urethra and the rectum. It is a rare entity. It is most often an iatrogenic lesion during prostate surgery. We present here the case of a post-traumatic urethro-rectal fistula secondary to a road accident. Surgical cure was via a perineal approach with gracilis flap interposition.

Case presentation

This is a 15-year-old patient who consulted for a urethro-cutaneous fistula. Retrograde urethrography (RUG) with voiding cystourethrography (VCUG) showed a urethro-rectal fistula, with contrast leakage and opacification of the rectum. The fistula was cured using an anterior perineal approach with interposition of a gracilis flap. The post-operative course was uneventful.

Discussion

Urethro-rectal fistula is a rare entity and most often iatrogenic. Due to the rarity of this entity, the literature concerning its description, and its treatment is poor. Tailored approach should be considered for each patient. The use of gracilis flap interposition is describe as a good technique for managing urethro-rectal fistulas.

Conclusion

Urethro-rectal fistula is a rare pathology, especially when it occurs following a road accident. Perineal cure with gracilis flap interposition appears to be a reliable technique.
导言尿道直肠瘘是尿道和直肠之间的异常沟通。这是一种罕见的疾病。它通常是前列腺手术中的先天性病变。我们在此介绍一例因交通事故继发的创伤后尿道直肠瘘。该病例是一名 15 岁患者,因尿道皮肤瘘就诊。逆行尿道造影术(RUG)和排尿膀胱造影术(VCUG)显示尿道直肠瘘,造影剂渗漏,直肠不透明。手术采用会阴前部入路,插入腓肠肌瓣,治愈了瘘管。讨论 尿道直肠瘘是一种罕见的疾病,多为先天性疾病。由于这种疾病的罕见性,有关其描述和治疗的文献很少。应考虑为每位患者量身定制治疗方法。结论尿道直肠瘘是一种罕见病,尤其是在交通事故后发生。使用腓肠肌瓣内插术进行会阴部治疗似乎是一种可靠的技术。
{"title":"Cure of urethro-rectal fistula secondary to a road traffic accident by perineal approach with gracilis flap interposition: A case report","authors":"M.L. Foba ,&nbsp;S.M.A. Fall ,&nbsp;F.J. Tchoungui Ritz ,&nbsp;B. Sine ,&nbsp;M. Beye ,&nbsp;A.A. Sankalé","doi":"10.1016/j.ijscr.2024.110564","DOIUrl":"10.1016/j.ijscr.2024.110564","url":null,"abstract":"<div><h3>Introduction</h3><div>A urethro-rectal fistula is an abnormal communication between the urethra and the rectum. It is a rare entity. It is most often an iatrogenic lesion during prostate surgery. We present here the case of a post-traumatic urethro-rectal fistula secondary to a road accident. Surgical cure was via a perineal approach with gracilis flap interposition.</div></div><div><h3>Case presentation</h3><div>This is a 15-year-old patient who consulted for a urethro-cutaneous fistula. Retrograde urethrography (RUG) with voiding cystourethrography (VCUG) showed a urethro-rectal fistula, with contrast leakage and opacification of the rectum. The fistula was cured using an anterior perineal approach with interposition of a gracilis flap. The post-operative course was uneventful.</div></div><div><h3>Discussion</h3><div>Urethro-rectal fistula is a rare entity and most often iatrogenic. Due to the rarity of this entity, the literature concerning its description, and its treatment is poor. Tailored approach should be considered for each patient. The use of gracilis flap interposition is describe as a good technique for managing urethro-rectal fistulas.</div></div><div><h3>Conclusion</h3><div>Urethro-rectal fistula is a rare pathology, especially when it occurs following a road accident. Perineal cure with gracilis flap interposition appears to be a reliable technique.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110564"},"PeriodicalIF":0.6,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142587238","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Incidental diagnosis of Mazabraud syndrome presenting as a lower extremity soft tissue mass: A case report and literature review 以下肢软组织肿块为表现的马扎布劳综合征的偶然诊断:病例报告与文献综述
IF 0.6 Q4 SURGERY Pub Date : 2024-11-04 DOI: 10.1016/j.ijscr.2024.110559
Hannia Isabel Cortez Marquina , Joab Rafael Galvan Bustillos , Jean Enrique Pierzo Morales , Fernando Cordera González de Cosío

Introduction and importance

Mazabraud's syndrome is a rare condition, describing the presence of fibrous bone dysplasia and intramuscular myxomas, with an incidence of 1:1,000,000. The aim of this article is to provide a review of the clinical presentation of Mazabraud's syndrome, including indications for surgical treatment, and follow-up strategies.

Case presentation

A 46-year-old woman presented with a 3-month history of a painless mass in the right gluteal region, she referred a rapid increase in the mass's volume in the 3 weeks prior to consultation. Physical examination revealed a solid, non-mobile mass adhered to the deep tissues of the right gluteal region. Magnetic resonance imaging (MRI) identified a probable intramuscular myxoma in the right gluteus, and incidentally evidenced an area suggestive of fibrous dysplasia in the left iliac bone. A total resection of the soft-tissue was performed, obtaining clear surgical margins. Pathology study confirmed the diagnosis of intramuscular myxoma. More than one year after surgical resection, the patient remains asymptomatic and has satisfactory results.

Clinical discussion

This case presented some unique features including a solitary myxoma, and contralateral fibrous dysplasia, surgical challenges included preoperative planning, as the myxoma was relatively large, and a careful resection to preserve the tumoral capsule, treatment included resection to attain clear margins, the sparing of healthy muscle proved to be valuable for a rapid postoperative recovery.

Conclusion

The diagnosis of Mazabraud's syndrome can be overlooked given its very low incidence. Resection is warranted in symptomatic cases and because of the risk of late recurrence, long-term follow-up is required after surgery.
导言和重要性:马扎布洛综合征是一种罕见病,描述了纤维性骨发育不良和肌肉内肌瘤的存在,发病率为1:1,000,000。本文旨在回顾马扎布劳综合征的临床表现,包括手术治疗的适应症和随访策略:一名 46 岁女性患者因右侧臀部无痛性肿块就诊 3 个月,就诊前 3 周肿块体积迅速增大。体格检查显示,右侧臀部深层组织中附着一个实性、不可移动的肿块。磁共振成像(MRI)发现右侧臀部可能存在肌内肌瘤,并意外发现左侧髂骨有一个纤维发育不良的区域。对软组织进行了全切除,手术边缘清晰。病理检查确诊为肌内肌瘤。手术切除一年多后,患者仍无症状,效果令人满意:临床讨论:该病例具有一些独特的特征,包括单发肌瘤和对侧纤维发育不良,手术挑战包括术前规划,因为肌瘤相对较大,以及小心切除以保留肿瘤囊,治疗包括切除以获得清晰的边缘,保留健康肌肉被证明对术后快速恢复很有价值:结论:马扎布洛综合征的发病率很低,可能会被忽视。结论:由于马扎布洛综合征的发病率极低,其诊断可能会被忽视。有症状的病例应进行切除,由于晚期复发的风险,术后需要长期随访。
{"title":"Incidental diagnosis of Mazabraud syndrome presenting as a lower extremity soft tissue mass: A case report and literature review","authors":"Hannia Isabel Cortez Marquina ,&nbsp;Joab Rafael Galvan Bustillos ,&nbsp;Jean Enrique Pierzo Morales ,&nbsp;Fernando Cordera González de Cosío","doi":"10.1016/j.ijscr.2024.110559","DOIUrl":"10.1016/j.ijscr.2024.110559","url":null,"abstract":"<div><h3>Introduction and importance</h3><div>Mazabraud's syndrome is a rare condition, describing the presence of fibrous bone dysplasia and intramuscular myxomas, with an incidence of 1:1,000,000. The aim of this article is to provide a review of the clinical presentation of Mazabraud's syndrome, including indications for surgical treatment, and follow-up strategies.</div></div><div><h3>Case presentation</h3><div>A 46-year-old woman presented with a 3-month history of a painless mass in the right gluteal region, she referred a rapid increase in the mass's volume in the 3 weeks prior to consultation. Physical examination revealed a solid, non-mobile mass adhered to the deep tissues of the right gluteal region. Magnetic resonance imaging (MRI) identified a probable intramuscular myxoma in the right gluteus, and incidentally evidenced an area suggestive of fibrous dysplasia in the left iliac bone. A total resection of the soft-tissue was performed, obtaining clear surgical margins. Pathology study confirmed the diagnosis of intramuscular myxoma. More than one year after surgical resection, the patient remains asymptomatic and has satisfactory results.</div></div><div><h3>Clinical discussion</h3><div>This case presented some unique features including a solitary myxoma, and contralateral fibrous dysplasia, surgical challenges included preoperative planning, as the myxoma was relatively large, and a careful resection to preserve the tumoral capsule, treatment included resection to attain clear margins, the sparing of healthy muscle proved to be valuable for a rapid postoperative recovery.</div></div><div><h3>Conclusion</h3><div>The diagnosis of Mazabraud's syndrome can be overlooked given its very low incidence. Resection is warranted in symptomatic cases and because of the risk of late recurrence, long-term follow-up is required after surgery.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110559"},"PeriodicalIF":0.6,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142630375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Minimally invasive ALL technique using the gracilis in the treatment of chronic ankle instabilities in athletes 利用腓肠肌的微创 ALL 技术治疗运动员的慢性踝关节不稳。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-03 DOI: 10.1016/j.ijscr.2024.110553
Omar Fadili , Mohammed Khodja , Oussama Hidoussi

Introduction and importance

Chronic ankle instability is a common issue in high-level athletes, affecting up to 48 % of lateral sprains. Rehabilitation strategies, including muscle strengthening, proprioceptive training, and range of motion exercises, often help but may not suffice, especially in sports that stress the ankle in a varus position. In such cases, surgery is required. Non-anatomic techniques have shown long-term ineffectiveness, while anatomical reconstructions with tissue augmentation are gaining favor.

Case and technique presentation

This study introduces the underreported ALL (Ankle Lateral Ligamentoplasty) technique, using gracilis tendon transfer for chronic ankle instability. This minimally invasive method restores the ruptured lateral collateral ligaments and preserves proprioceptive and anatomical stability, with the added benefit of sparing the semitendinosus tendon for potential knee surgery.

Discussion

The surgical procedure allows immediate walking post-op with progressive recovery, including early mobilization, brace use by the fourth week, and return to pivot sports by the third month. Compared to tenodesis procedures, anatomical reconstruction offers superior stability and mobility, faster recovery, and less risk of degenerative arthritis.

Conclusion

The ALL technique shows promise in treating chronic ankle instability in athletes, providing effective stabilization while preserving ankle function. However, further studies are needed to validate its widespread clinical use.
导言和重要性:慢性踝关节不稳是高水平运动员的常见问题,在外侧扭伤中占 48%。包括肌肉强化、本体感觉训练和活动范围练习在内的康复策略通常会有所帮助,但可能并不足够,尤其是在踝关节受力于外翻位置的运动中。在这种情况下,需要进行手术治疗。非解剖技术显示长期无效,而通过组织增量进行解剖重建则越来越受到青睐:本研究介绍了未被充分报道的踝关节外侧韧带成形术(ALL)技术,该技术使用擒拿肌腱转移治疗慢性踝关节不稳定。这种微创方法能恢复断裂的外侧副韧带,保持本体感觉和解剖稳定性,还能保留半腱肌腱,以备膝关节手术之用:讨论:该手术方法允许术后立即行走并逐步恢复,包括早期活动,第四周使用支具,第三个月恢复枢轴运动。与腱鞘切除术相比,解剖重建术具有更高的稳定性和活动度,恢复更快,发生退行性关节炎的风险更低:ALL技术有望治疗运动员的慢性踝关节不稳,在提供有效稳定的同时保护踝关节功能。然而,还需要进一步的研究来验证其在临床上的广泛应用。
{"title":"Minimally invasive ALL technique using the gracilis in the treatment of chronic ankle instabilities in athletes","authors":"Omar Fadili ,&nbsp;Mohammed Khodja ,&nbsp;Oussama Hidoussi","doi":"10.1016/j.ijscr.2024.110553","DOIUrl":"10.1016/j.ijscr.2024.110553","url":null,"abstract":"<div><h3>Introduction and importance</h3><div>Chronic ankle instability is a common issue in high-level athletes, affecting up to 48 % of lateral sprains. Rehabilitation strategies, including muscle strengthening, proprioceptive training, and range of motion exercises, often help but may not suffice, especially in sports that stress the ankle in a varus position. In such cases, surgery is required. Non-anatomic techniques have shown long-term ineffectiveness, while anatomical reconstructions with tissue augmentation are gaining favor.</div></div><div><h3>Case and technique presentation</h3><div>This study introduces the underreported ALL (Ankle Lateral Ligamentoplasty) technique, using gracilis tendon transfer for chronic ankle instability. This minimally invasive method restores the ruptured lateral collateral ligaments and preserves proprioceptive and anatomical stability, with the added benefit of sparing the semitendinosus tendon for potential knee surgery.</div></div><div><h3>Discussion</h3><div>The surgical procedure allows immediate walking post-op with progressive recovery, including early mobilization, brace use by the fourth week, and return to pivot sports by the third month. Compared to tenodesis procedures, anatomical reconstruction offers superior stability and mobility, faster recovery, and less risk of degenerative arthritis.</div></div><div><h3>Conclusion</h3><div>The ALL technique shows promise in treating chronic ankle instability in athletes, providing effective stabilization while preserving ankle function. However, further studies are needed to validate its widespread clinical use.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110553"},"PeriodicalIF":0.6,"publicationDate":"2024-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142607003","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Necrotizing fasciitis in a pediatric patient: Successful management in the inguinal area - A case report 一名儿童患者的坏死性筋膜炎:腹股沟区的成功治疗--病例报告
IF 0.6 Q4 SURGERY Pub Date : 2024-11-03 DOI: 10.1016/j.ijscr.2024.110550
Anna Ntanika , Adelais Tzortzopoulou , Ioanna Argyri , Artemis Dendi , Orthodoxos Achilleos

Introduction

Necrotizing fasciitis (NF) is a rare life-threatening medical and surgical emergency. We present a case of a pediatric patient diagnosed with necrotizing fasciitis in the inguinal area which required debridement and post-operative management of the residual wound using a combination of wound closure techniques.

Case presentation

A 10-months-old girl with a history of Food-protein induced enterocolitis syndrome (FPIES) presented with septic shock and ulcerative lesions of the inguinal area. She was admitted to the Intensive Care Unit (ICU) of our hospital, antibiotic treatment was administered and a diverting colostomy was performed. Serial surgical debridement of the affected tissues resulted in an extensive tissue deficit. Management of the residual skin and soft tissues deficit included application of Negative Pressure Wound Therapy (NPWT) with Vacuum-Assisted Closure (VAC) and was followed by Oasis® extracellular matrix (ECM) graft placement. After 65 days of hospitalization, the wound surface was completely epithelialized.

Discussion

A challenging aspect of NF management is the closure of the residual skin and soft tissue deficit after surgical debridement. Considering the patient's characteristics, a less invasive reconstructive technique was sought. Application of NPWT followed by ECM graft placement are two effective options that can be combined in different stages of wound healing.

Conclusions

The management of the residual wound after surgical debridement of the affected tissue in NF requires a patient – specific approach and constant reevaluation of the management plan. NPWT and ECM graft placement can significantly contribute to wound closure and epithelization of the residual deficit in children.
导言:坏死性筋膜炎(NF)是一种罕见的危及生命的内外科急症。我们介绍了一例被诊断为腹股沟部位坏死性筋膜炎的儿科患者,该患者需要进行清创,并在术后使用多种伤口闭合技术处理残留伤口。病例介绍 一名 10 个月大的女孩,曾患食物蛋白诱发的小肠结肠炎综合征(FPIES),出现脓毒性休克和腹股沟部位溃疡性病变。她被送入本院重症监护室(ICU),接受了抗生素治疗,并进行了结肠造口术。对受影响的组织进行了连续的手术清创,造成了广泛的组织缺损。处理残余皮肤和软组织缺损的方法包括应用负压伤口疗法(NPWT)和真空辅助闭合术(VAC),随后进行 Oasis® 细胞外基质(ECM)移植。住院 65 天后,伤口表面完全上皮化。讨论 NF 管理的一个挑战是手术清创后残余皮肤和软组织缺损的闭合。考虑到患者的特点,我们寻求了一种创伤较小的重建技术。应用 NPWT 和 ECM 移植是两种有效的方法,可在伤口愈合的不同阶段结合使用。结论 NF 受影响组织手术清创后残留伤口的处理需要针对患者的具体情况,并不断重新评估处理方案。NPWT 和 ECM 移植置入可显著促进儿童伤口闭合和残余缺损上皮化。
{"title":"Necrotizing fasciitis in a pediatric patient: Successful management in the inguinal area - A case report","authors":"Anna Ntanika ,&nbsp;Adelais Tzortzopoulou ,&nbsp;Ioanna Argyri ,&nbsp;Artemis Dendi ,&nbsp;Orthodoxos Achilleos","doi":"10.1016/j.ijscr.2024.110550","DOIUrl":"10.1016/j.ijscr.2024.110550","url":null,"abstract":"<div><h3>Introduction</h3><div>Necrotizing fasciitis (NF) is a rare life-threatening medical and surgical emergency. We present a case of a pediatric patient diagnosed with necrotizing fasciitis in the inguinal area which required debridement and post-operative management of the residual wound using a combination of wound closure techniques.</div></div><div><h3>Case presentation</h3><div>A 10-months-old girl with a history of Food-protein induced enterocolitis syndrome (FPIES) presented with septic shock and ulcerative lesions of the inguinal area. She was admitted to the Intensive Care Unit (ICU) of our hospital, antibiotic treatment was administered and a diverting colostomy was performed. Serial surgical debridement of the affected tissues resulted in an extensive tissue deficit. Management of the residual skin and soft tissues deficit included application of Negative Pressure Wound Therapy (NPWT) with Vacuum-Assisted Closure (VAC) and was followed by Oasis® extracellular matrix (ECM) graft placement. After 65 days of hospitalization, the wound surface was completely epithelialized.</div></div><div><h3>Discussion</h3><div>A challenging aspect of NF management is the closure of the residual skin and soft tissue deficit after surgical debridement. Considering the patient's characteristics, a less invasive reconstructive technique was sought. Application of NPWT followed by ECM graft placement are two effective options that can be combined in different stages of wound healing.</div></div><div><h3>Conclusions</h3><div>The management of the residual wound after surgical debridement of the affected tissue in NF requires a patient – specific approach and constant reevaluation of the management plan. NPWT and ECM graft placement can significantly contribute to wound closure and epithelization of the residual deficit in children.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110550"},"PeriodicalIF":0.6,"publicationDate":"2024-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142592694","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Gastric collision tumor of adenocarcinoma and MALT lymphoma: A rare case report and literature review 腺癌和 MALT 淋巴瘤的胃碰撞瘤:罕见病例报告和文献综述
IF 0.6 Q4 SURGERY Pub Date : 2024-11-03 DOI: 10.1016/j.ijscr.2024.110556
Ahmed Omry , Wael Ferjaoui , Sadok Megdiche , Sahir Omrani , Sana Ben Slama , Dhouha Bacha

Introduction and importance

Gastric collision tumors, characterized by the coexistence of two distinct malignancies within the same organ, are exceptionally rare. We report a case involving a gastric collision tumor composed of adenocarcinoma (ADK) and marginal zone lymphoma, diagnosed postoperatively. To date, only six cases of MALT lymphoma as part of gastric collision tumors have been published, highlighting the rarity of this association.

Clinical presentation

A 58-year-old male with type 2 diabetes and a family history of breast cancer presented with six months of anemia and epigastric pain. Endoscopy showed a 5 cm ulcerated, friable gastric mass, and biopsies indicated a low-grade tubular adenocarcinoma. Imaging revealed gastric wall thickening and lymphadenopathy. He received FLOT chemotherapy followed by total gastrectomy with Roux-en-Y reconstruction. Histopathology confirmed a gastric collision tumor with a minimal adenocarcinoma remnant and extensive MALT lymphoma.

Discussion

Collision tumors are rare and present unique diagnostic and therapeutic challenges due to the coexistence of distinct malignancies. This case highlights the complexity of managing such tumors, as accurate diagnosis requires comprehensive histopathological analysis. The dual presence of adenocarcinoma and MALT lymphoma necessitated a tailored approach with FLOT chemotherapy and total gastrectomy. The patient's ongoing adjuvant chemotherapy emphasizes the need for vigilant, long-term follow-up to monitor for recurrence and potential metachronous malignancies.

Conclusion

Gastric collision tumors involving ADK and MALT lymphoma are rare and challenging. This case contributes to the limited literature on collision tumors, highlighting the necessity for comprehensive diagnostic and therapeutic strategies.
导言和重要性胃碰撞瘤的特点是在同一器官内同时存在两种不同的恶性肿瘤,但这种情况非常罕见。我们报告了一例由腺癌(ADK)和边缘区淋巴瘤组成的胃碰撞瘤,并在术后确诊。临床表现一名 58 岁男性,患有 2 型糖尿病,有乳腺癌家族史,六个月前出现贫血和上腹痛。内镜检查发现一个 5 厘米的溃疡性易碎胃肿块,活检显示为低级别管状腺癌。影像学检查显示胃壁增厚和淋巴结肿大。他接受了FLOT化疗,随后接受了全胃切除术和Roux-en-Y重建术。组织病理学证实为胃碰撞瘤,伴有极少量腺癌残留和广泛的 MALT 淋巴瘤。讨论碰撞瘤非常罕见,由于同时存在不同的恶性肿瘤,给诊断和治疗带来了独特的挑战。本病例凸显了此类肿瘤治疗的复杂性,因为准确诊断需要全面的组织病理学分析。由于患者同时患有腺癌和 MALT 淋巴瘤,因此必须采用 FLOT 化疗和全胃切除术。该患者正在接受辅助化疗,这强调了长期随访的必要性,以监测复发和潜在的并发恶性肿瘤。本病例为有关碰撞性肿瘤的有限文献做出了贡献,强调了综合诊断和治疗策略的必要性。
{"title":"Gastric collision tumor of adenocarcinoma and MALT lymphoma: A rare case report and literature review","authors":"Ahmed Omry ,&nbsp;Wael Ferjaoui ,&nbsp;Sadok Megdiche ,&nbsp;Sahir Omrani ,&nbsp;Sana Ben Slama ,&nbsp;Dhouha Bacha","doi":"10.1016/j.ijscr.2024.110556","DOIUrl":"10.1016/j.ijscr.2024.110556","url":null,"abstract":"<div><h3>Introduction and importance</h3><div>Gastric collision tumors, characterized by the coexistence of two distinct malignancies within the same organ, are exceptionally rare. We report a case involving a gastric collision tumor composed of adenocarcinoma (ADK) and marginal zone lymphoma, diagnosed postoperatively. To date, only six cases of MALT lymphoma as part of gastric collision tumors have been published, highlighting the rarity of this association.</div></div><div><h3>Clinical presentation</h3><div>A 58-year-old male with type 2 diabetes and a family history of breast cancer presented with six months of anemia and epigastric pain. Endoscopy showed a 5 cm ulcerated, friable gastric mass, and biopsies indicated a low-grade tubular adenocarcinoma. Imaging revealed gastric wall thickening and lymphadenopathy. He received FLOT chemotherapy followed by total gastrectomy with Roux-en-Y reconstruction. Histopathology confirmed a gastric collision tumor with a minimal adenocarcinoma remnant and extensive MALT lymphoma.</div></div><div><h3>Discussion</h3><div>Collision tumors are rare and present unique diagnostic and therapeutic challenges due to the coexistence of distinct malignancies. This case highlights the complexity of managing such tumors, as accurate diagnosis requires comprehensive histopathological analysis. The dual presence of adenocarcinoma and MALT lymphoma necessitated a tailored approach with FLOT chemotherapy and total gastrectomy. The patient's ongoing adjuvant chemotherapy emphasizes the need for vigilant, long-term follow-up to monitor for recurrence and potential metachronous malignancies.</div></div><div><h3>Conclusion</h3><div>Gastric collision tumors involving ADK and MALT lymphoma are rare and challenging. This case contributes to the limited literature on collision tumors, highlighting the necessity for comprehensive diagnostic and therapeutic strategies.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110556"},"PeriodicalIF":0.6,"publicationDate":"2024-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142578590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Primary cardiac myxofibrosarcoma in a patient with Ebstein's anomaly: First reported case 埃布斯坦畸形患者的原发性心脏肌纤维肉瘤:首例报告病例
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 DOI: 10.1016/j.ijscr.2024.110551
Nisha Modi , Sami Anwar Khan , Vikas Asati , Shivani Kapur , Amit Varma

Introduction

Primary Cardiac Myxofibrosarcoma (PCM) is a rare and aggressive cardiac malignancy, accounting for less than 1 % of primary cardiac tumors. It can occur infrequently with congenital heart defects like Ebstein's anomaly (EA), characterized by a malformed tricuspid valve. PCM often presents as a painless cardiac mass, leading to potential delays in diagnosis and treatment.

Presentation of case

We present the case of a 38-year-old female with a history of EA who presented with dyspnea. Echocardiography revealed severe tricuspid regurgitation and a mobile mass in the left atrium, which prolapsed through the mitral valve with each heartbeat. Intraoperative findings confirmed a lobulated mass. Histological analysis showed a multinodular spindle cell tumor within a myxoid stroma, featuring long, curvilinear blood vessels, few hypocellular myxomatous areas, and focal necrosis. Immunohistochemical staining revealed positivity for TLE1 and SMA, while the tumor was negative for AE1/AE3, S100, desmin, CD34, HMB45, and CD117, leading to a diagnosis of PCM.

Discussion

Initially suspected to be a myxoma, histopathological findings confirmed PCM, notably characterized by prominent thin-walled blood vessels. This highlights the importance of thorough pathological evaluation. This case is the first reported instance of PCM associated with EA, contributing to the limited literature on this rare combination.

Conclusion

Malignant tumors should be included in the differential diagnosis of cardiac masses. Prompt diagnosis and complete surgical resection are essential for improving patient outcomes and reducing the risk of recurrence.
导言原发性心脏肌纤维肉瘤(PCM)是一种罕见的侵袭性心脏恶性肿瘤,占原发性心脏肿瘤的比例不到 1%。先天性心脏缺陷(如以三尖瓣畸形为特征的爱布斯坦氏畸形(EA))也会导致该病的发生,但这种情况并不多见。PCM 常表现为无痛性心脏肿块,可能导致诊断和治疗的延误。超声心动图显示左心房有严重的三尖瓣反流和移动性肿块,每次心跳时肿块都会脱出二尖瓣。术中检查结果证实这是一个分叶状肿块。组织学分析显示,肌基质内为多结节纺锤形细胞瘤,具有长而弯曲的血管、少量细胞减少的肌瘤区和灶性坏死。免疫组化染色显示 TLE1 和 SMA 阳性,而 AE1/AE3、S100、desmin、CD34、HMB45 和 CD117 阴性,因此诊断为 PCM。这凸显了彻底病理评估的重要性。本病例是首次报道 PCM 与 EA 相关的病例,为有关这种罕见组合的有限文献做出了贡献。及时诊断和彻底手术切除对改善患者预后和降低复发风险至关重要。
{"title":"Primary cardiac myxofibrosarcoma in a patient with Ebstein's anomaly: First reported case","authors":"Nisha Modi ,&nbsp;Sami Anwar Khan ,&nbsp;Vikas Asati ,&nbsp;Shivani Kapur ,&nbsp;Amit Varma","doi":"10.1016/j.ijscr.2024.110551","DOIUrl":"10.1016/j.ijscr.2024.110551","url":null,"abstract":"<div><h3>Introduction</h3><div>Primary Cardiac Myxofibrosarcoma (PCM) is a rare and aggressive cardiac malignancy, accounting for less than 1 % of primary cardiac tumors. It can occur infrequently with congenital heart defects like Ebstein's anomaly (EA), characterized by a malformed tricuspid valve. PCM often presents as a painless cardiac mass, leading to potential delays in diagnosis and treatment.</div></div><div><h3>Presentation of case</h3><div>We present the case of a 38-year-old female with a history of EA who presented with dyspnea. Echocardiography revealed severe tricuspid regurgitation and a mobile mass in the left atrium, which prolapsed through the mitral valve with each heartbeat. Intraoperative findings confirmed a lobulated mass. Histological analysis showed a multinodular spindle cell tumor within a myxoid stroma, featuring long, curvilinear blood vessels, few hypocellular myxomatous areas, and focal necrosis. Immunohistochemical staining revealed positivity for TLE1 and SMA, while the tumor was negative for AE1/AE3, S100, desmin, CD34, HMB45, and CD117, leading to a diagnosis of PCM.</div></div><div><h3>Discussion</h3><div>Initially suspected to be a myxoma, histopathological findings confirmed PCM, notably characterized by prominent thin-walled blood vessels. This highlights the importance of thorough pathological evaluation. This case is the first reported instance of PCM associated with EA, contributing to the limited literature on this rare combination.</div></div><div><h3>Conclusion</h3><div>Malignant tumors should be included in the differential diagnosis of cardiac masses. Prompt diagnosis and complete surgical resection are essential for improving patient outcomes and reducing the risk of recurrence.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110551"},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142587239","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Traumatic anterior fracture dislocation of the humeral head. A rare case report. 肱骨头外伤性前方骨折脱位。罕见病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-17 DOI: 10.1016/j.ijscr.2024.110469
Tumwesige R Kondo, Michael Mapunda, Tangai Mwanga, Peter Magembe Mrimba, Rogers J Temu, Godlisten S Kawiche

Introduction: Anterior fracture dislocation of the humerus with an anatomical neck fracture is an uncommon injury. These injuries pose a significant risk of devastating complications, such as avascular necrosis of the humeral head, due to the poor vascularization of the area, and stiffness resulting from prolonged immobilization.

Clinical presentation: We report a case of a 20-year-old female who was involved in a motor vehicle crash and sustained an anterior fracture dislocation of the humerus with an anatomical neck fracture. The injury was successfully managed with open reduction and internal fixation using a plate and screws. Given the rarity of this type of injury, this case provides valuable insights into its management and prognosis.

Discussion: Proximal humeral fractures are common injuries, although fractures at the level of the anatomical neck are less common in orthopedic traumatology. The management of these injuries is guided by factors such as fracture morphology, displacement, potential disruption to blood supply, bone quality, patient's age, and functional demands. Various surgical management strategies have been proposed, emphasizing early intervention to minimize the risk of complications.

Conclusion: This case aims to highlight the importance of the value of early operative intervention, good anatomic reduction with stable fixation, and the importance of early mobilization of the shoulder to achieve favorable outcomes and minimize complications such as stiffness in patients with this type of injury.

简介肱骨前方骨折脱位伴解剖学颈骨折是一种不常见的损伤。这种损伤极易导致破坏性并发症,如肱骨头血管坏死,因为该区域血管通畅不良,以及长期固定导致的僵硬:我们报告了一例 20 岁女性的病例,她在一次车祸中肱骨前部骨折脱位,并伴有解剖学颈骨折。经过切开复位和使用钢板和螺钉进行内固定,伤情得到了成功控制。鉴于此类损伤的罕见性,本病例为其治疗和预后提供了宝贵的见解:讨论:肱骨近端骨折是常见的损伤,但在创伤骨科中,解剖颈水平的骨折并不常见。这些损伤的处理需要考虑骨折形态、移位、潜在的血供破坏、骨质、患者年龄和功能需求等因素。目前已提出了多种手术治疗策略,强调早期干预以最大限度地降低并发症风险:本病例旨在强调早期手术干预、良好的解剖复位和稳定的固定以及肩部早期活动的重要性,以获得良好的治疗效果,并将此类损伤患者的僵硬等并发症降至最低。
{"title":"Traumatic anterior fracture dislocation of the humeral head. A rare case report.","authors":"Tumwesige R Kondo, Michael Mapunda, Tangai Mwanga, Peter Magembe Mrimba, Rogers J Temu, Godlisten S Kawiche","doi":"10.1016/j.ijscr.2024.110469","DOIUrl":"10.1016/j.ijscr.2024.110469","url":null,"abstract":"<p><strong>Introduction: </strong>Anterior fracture dislocation of the humerus with an anatomical neck fracture is an uncommon injury. These injuries pose a significant risk of devastating complications, such as avascular necrosis of the humeral head, due to the poor vascularization of the area, and stiffness resulting from prolonged immobilization.</p><p><strong>Clinical presentation: </strong>We report a case of a 20-year-old female who was involved in a motor vehicle crash and sustained an anterior fracture dislocation of the humerus with an anatomical neck fracture. The injury was successfully managed with open reduction and internal fixation using a plate and screws. Given the rarity of this type of injury, this case provides valuable insights into its management and prognosis.</p><p><strong>Discussion: </strong>Proximal humeral fractures are common injuries, although fractures at the level of the anatomical neck are less common in orthopedic traumatology. The management of these injuries is guided by factors such as fracture morphology, displacement, potential disruption to blood supply, bone quality, patient's age, and functional demands. Various surgical management strategies have been proposed, emphasizing early intervention to minimize the risk of complications.</p><p><strong>Conclusion: </strong>This case aims to highlight the importance of the value of early operative intervention, good anatomic reduction with stable fixation, and the importance of early mobilization of the shoulder to achieve favorable outcomes and minimize complications such as stiffness in patients with this type of injury.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"124 ","pages":"110469"},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11532452/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142477869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Case report: Novel approach to distal radius non-union treatment with free fibula flap reconstruction. 病例报告:用游离腓骨瓣重建治疗桡骨远端不愈合的新方法。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-11 DOI: 10.1016/j.ijscr.2024.110447
Maria Albuquerque, Luís Mata Ribeiro, Miguel Botton

Introduction: Distal radius fractures are common among adults. Despite being a rare complication, occurring in only 0.2 % of the cases, non-union poses significant treatment challenges.

Presentation of case: In this article, we report the case of a 43-year-old male with a history of distal radius fracture resulting from a motorcycle accident. His initial treatment consisted of external fixation followed by a distraction plate and internal fixation with volar plate and screws. Due to plate breakage, he underwent refixation with a volar plate and autologous bone graft six months after the accident. However, five months after surgery, CT-scans showed a radius non-union. This led to a multidisciplinary approach involving orthopaedic and plastic surgery teams, where the patient underwent distal radius reconstruction using a free fibula flap. Postoperative recovery led to favourable outcomes with evidence of bony consolidation at six-month follow-up.

Discussion: Conventional techniques for distal radius non-union treatment may fall short in achieving bony continuity in a non-suitable soft tissue environment. Free vascularised fibular flap has emerged as a primary option for long bone reconstruction, offering advantages such as anatomical compatibility and immediate structural support.

Conclusion: This case highlights the efficacy of free fibular flap in addressing complex distal radius non-unions, providing an effective solution when simpler techniques have failed.

简介桡骨远端骨折在成年人中很常见。尽管桡骨远端骨折是一种罕见的并发症,发生率仅为 0.2%,但不愈合给治疗带来了巨大挑战:本文报告了一例因摩托车事故导致桡骨远端骨折的 43 岁男性病例。他最初的治疗包括外固定,然后是牵引钢板和用沃尔钢板和螺钉进行内固定。由于钢板断裂,他在事故发生 6 个月后又接受了用腓骨钢板和自体骨移植重新固定的手术。然而,术后五个月,CT 扫描显示桡骨未愈合。因此,骨科和整形外科团队采取了多学科方法,使用游离腓骨瓣对患者进行了桡骨远端重建。术后恢复良好,随访6个月后骨质得到巩固:讨论:传统的桡骨远端骨不连治疗技术可能无法在不适合的软组织环境中实现骨性连续性。游离血管化纤维皮瓣已成为长骨重建的主要选择,具有解剖相容性和即时结构支持等优势:本病例凸显了游离腓骨瓣在治疗复杂的桡骨远端不连接方面的功效,在简单技术失败后提供了有效的解决方案。
{"title":"Case report: Novel approach to distal radius non-union treatment with free fibula flap reconstruction.","authors":"Maria Albuquerque, Luís Mata Ribeiro, Miguel Botton","doi":"10.1016/j.ijscr.2024.110447","DOIUrl":"10.1016/j.ijscr.2024.110447","url":null,"abstract":"<p><strong>Introduction: </strong>Distal radius fractures are common among adults. Despite being a rare complication, occurring in only 0.2 % of the cases, non-union poses significant treatment challenges.</p><p><strong>Presentation of case: </strong>In this article, we report the case of a 43-year-old male with a history of distal radius fracture resulting from a motorcycle accident. His initial treatment consisted of external fixation followed by a distraction plate and internal fixation with volar plate and screws. Due to plate breakage, he underwent refixation with a volar plate and autologous bone graft six months after the accident. However, five months after surgery, CT-scans showed a radius non-union. This led to a multidisciplinary approach involving orthopaedic and plastic surgery teams, where the patient underwent distal radius reconstruction using a free fibula flap. Postoperative recovery led to favourable outcomes with evidence of bony consolidation at six-month follow-up.</p><p><strong>Discussion: </strong>Conventional techniques for distal radius non-union treatment may fall short in achieving bony continuity in a non-suitable soft tissue environment. Free vascularised fibular flap has emerged as a primary option for long bone reconstruction, offering advantages such as anatomical compatibility and immediate structural support.</p><p><strong>Conclusion: </strong>This case highlights the efficacy of free fibular flap in addressing complex distal radius non-unions, providing an effective solution when simpler techniques have failed.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"124 ","pages":"110447"},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11535361/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142477870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hemolytic reaction after major and minor compatible blood transfusion for a cesarean section patient in a resource-limited area: A case report. 在一个资源有限的地区,一名剖腹产患者在输注了大分子和小分子相容血液后出现溶血反应:病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-15 DOI: 10.1016/j.ijscr.2024.110426
Sintayehu Samuel, Hunde Amsalu, Deginet Tesfaye, Yisehak Wolde

Introduction: A hemolytic transfusion reaction is the destruction of red blood cells caused by immunological incompatibility between the donor and the recipient, not only incompatibility but also, rarely, compatible blood transfusion, which may cause a hemolytic transfusion reaction. A hemolytic transfusion reaction occurs when the transfusion causes symptoms as well as clinical or laboratory indicators of increased red cell death.

Patient presentation: We present the case of a 27-year-old Gravida II Para I mother who was blood group AB positive with anaemia, hypotension secondary to antepartum hemorrhage, and a mentally conscious mother who was transferred to our obstetric emergency operation theatre. As she experienced bleeding on arrival, we assessed the patient's history and performed anaesthesia-related physical examinations, such as cardiovascular examination, respiratory examination, central nerve system examination, and airway examination. We followed the patient postoperatively until discharge from the hospital, and 12.9 g/dl hemoglobin, 36.3 % haematocrit, 402 × 103 platelet count, and 0.9 mg/dl creatinine were detected. After satisfactory postoperative vital signs and laboratory results were obtained, the patient was discharged from the hospital after 3 days.

Clinical discussion: Acute hemolytic transfusion is a medical emergency with an estimated frequency of one per 70,000 blood product transfusions and an estimated fatality rate of five per 10 million RBC unit transfusions. Importantly, the traditional triad of fever, flank pain, and red or dark urine is uncommon. However, these symptoms may not be immediately visible if the patient is under anaesthesia; in such circumstances, seeping from venipuncture and dark urine caused by DIC and hemoglobinuria, respectively, may be the only observations.

Conclusion: Blood transfusion is performed in 0.5-3 % of women with obstetric hemorrhage and accounts for 1 % of all transfused blood products in high-income countries. Anesthesiologists face a significant issue in identifying the necessity for transfusion in patients with obstetric hemorrhage. Hemolytic reactions after blood transfusion are common during emergency patient management. For this reason, the World Health Organization has developed guidelines for early detection and management.

导言溶血性输血反应是指供血者和受血者之间因免疫不相容而引起的红细胞破坏,不仅是不相容的输血,在极少数情况下,相容的输血也可能引起溶血性输血反应。当输血引起症状以及红细胞死亡增加的临床或实验室指标时,就会发生溶血性输血反应:本病例是一位 27 岁的 Gravida II Para I 型产妇,血型 AB 阳性,贫血,低血压,继发于产前出血,神志清醒,被转送到我们的产科急诊手术室。由于她在到达时出现出血,我们评估了患者的病史,并进行了与麻醉相关的体格检查,如心血管检查、呼吸系统检查、中枢神经系统检查和气道检查。我们对患者进行了术后随访,直至出院,检测到血红蛋白 12.9 g/dl、血细胞比容 36.3 %、血小板 402 × 103、肌酐 0.9 mg/dl。在获得满意的术后生命体征和实验室结果后,患者于 3 天后出院:急性溶血性输血是一种医疗急症,估计每 7 万次血液制品输血中就会发生一次,估计每 1 千万次红细胞单位输血中就会出现 5 例死亡病例。重要的是,传统的发烧、腹痛、尿红或尿黑三联症并不常见。然而,如果患者处于麻醉状态,这些症状可能无法立即显现;在这种情况下,静脉穿刺渗血和由 DIC 和血红蛋白尿引起的深色尿液可能是唯一的观察结果:结论:在高收入国家,0.5%-3% 的产科出血妇女需要输血,占输血总量的 1%。麻醉医师在确定产科出血患者是否需要输血时面临着一个重大问题。输血后的溶血反应在急诊病人管理中很常见。为此,世界卫生组织制定了早期检测和处理指南。
{"title":"Hemolytic reaction after major and minor compatible blood transfusion for a cesarean section patient in a resource-limited area: A case report.","authors":"Sintayehu Samuel, Hunde Amsalu, Deginet Tesfaye, Yisehak Wolde","doi":"10.1016/j.ijscr.2024.110426","DOIUrl":"10.1016/j.ijscr.2024.110426","url":null,"abstract":"<p><strong>Introduction: </strong>A hemolytic transfusion reaction is the destruction of red blood cells caused by immunological incompatibility between the donor and the recipient, not only incompatibility but also, rarely, compatible blood transfusion, which may cause a hemolytic transfusion reaction. A hemolytic transfusion reaction occurs when the transfusion causes symptoms as well as clinical or laboratory indicators of increased red cell death.</p><p><strong>Patient presentation: </strong>We present the case of a 27-year-old Gravida II Para I mother who was blood group AB positive with anaemia, hypotension secondary to antepartum hemorrhage, and a mentally conscious mother who was transferred to our obstetric emergency operation theatre. As she experienced bleeding on arrival, we assessed the patient's history and performed anaesthesia-related physical examinations, such as cardiovascular examination, respiratory examination, central nerve system examination, and airway examination. We followed the patient postoperatively until discharge from the hospital, and 12.9 g/dl hemoglobin, 36.3 % haematocrit, 402 × 10<sup>3</sup> platelet count, and 0.9 mg/dl creatinine were detected. After satisfactory postoperative vital signs and laboratory results were obtained, the patient was discharged from the hospital after 3 days.</p><p><strong>Clinical discussion: </strong>Acute hemolytic transfusion is a medical emergency with an estimated frequency of one per 70,000 blood product transfusions and an estimated fatality rate of five per 10 million RBC unit transfusions. Importantly, the traditional triad of fever, flank pain, and red or dark urine is uncommon. However, these symptoms may not be immediately visible if the patient is under anaesthesia; in such circumstances, seeping from venipuncture and dark urine caused by DIC and hemoglobinuria, respectively, may be the only observations.</p><p><strong>Conclusion: </strong>Blood transfusion is performed in 0.5-3 % of women with obstetric hemorrhage and accounts for 1 % of all transfused blood products in high-income countries. Anesthesiologists face a significant issue in identifying the necessity for transfusion in patients with obstetric hemorrhage. Hemolytic reactions after blood transfusion are common during emergency patient management. For this reason, the World Health Organization has developed guidelines for early detection and management.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"124 ","pages":"110426"},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11530600/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142477879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
International Journal of Surgery Case Reports
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1