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Bladder injury caused by a urachal remnant during laparoscopic ileocecal resection: A case report. 腹腔镜回盲部切除术中由尿道残余物造成的膀胱损伤:病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-12 DOI: 10.1016/j.ijscr.2024.110597
Takenori Segawa, Mizunori Yaegashi, Yuichiro Hirata, Noriyuki Sasaki, Akira Sasaki

Introduction: Bladder injuries that occur during laparoscopic surgery are rare but a serious complication. In particular, patients with urachal remnants have a high risk for bladder injuries during suprapubic port insertion. We report the case of a bladder injury caused by a urachal remnant during laparoscopic ileocecal resection for cecal cancer.

Case presentation: A 46-year-old man diagnosed with cT2, N0, M0, stage I cecal cancer underwent laparoscopic ileocecal resection. A suprapubic port was inserted under direct vision. After ileocecal resection, a bladder injury was discovered after the removal of the suprapubic port. The suprapubic port wound was extended to reveal the bladder wall around the injury, and the injury was sutured. During surgery, preoperative computed tomography (CT) results were reviewed, and sagittal CT revealed a urachal remnant. The postoperative course was uneventful, and the patient was discharged 10 days after surgery.

Discussion: Urachal remnants are rare in adults. This case emphasizes that although it is difficult to diagnose asymptomatic urachal remnants preoperatively, sagittal CT scans may aid in the diagnosis. Careful consideration of port placement and preoperative urethral catheter insertion is important to prevent bladder injuries in cases of urachal remnants.

Conclusion: Sagittal CT scans are considered effective in detecting diverticulum-type urachal remnants. Port placement without the need for a suprapubic trocar should be considered in cases with urachal remnants.

简介腹腔镜手术中发生的膀胱损伤虽然罕见,但却是一种严重的并发症。特别是有尿道残留物的患者,在耻骨上插孔插入时发生膀胱损伤的风险很高。我们报告了一例在腹腔镜回盲部切除术治疗盲肠癌过程中因尿道残余物导致膀胱损伤的病例:一名 46 岁男子被诊断为 cT2、N0、M0、I 期盲肠癌,接受了腹腔镜回盲部切除术。在直视下插入耻骨上端口。回盲部切除术后,拔出耻骨上端口后发现膀胱损伤。扩大耻骨上端口伤口,露出损伤周围的膀胱壁,并缝合损伤处。手术期间,对术前计算机断层扫描(CT)结果进行了复查,矢状位 CT 显示有尿道残余。术后过程顺利,患者术后 10 天出院:讨论:尿道残余在成人中很少见。本病例强调,虽然术前很难诊断无症状的泌尿道残余,但矢状面 CT 扫描可能有助于诊断。慎重考虑端口放置和术前尿道导管插入对于防止膀胱残余尿道病例中的膀胱损伤非常重要:结论:矢状位 CT 扫描可有效检测憩室型残余尿道。有尿道残余的病例应考虑无需耻骨上套管的造口置入术。
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引用次数: 0
Case report of simultaneous phlegmasia cerulea dolens and acute limb ischemia 同时伴有痰多和急性肢体缺血的病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-12 DOI: 10.1016/j.ijscr.2024.110596
Smoter Šimon, Slyško Roman

Introduction

Phlegmasia cerulea dolens (PCD) is a rare, life- and limb-threatening condition of acute massive deep vein thrombosis (DVT) that requires emergent therapeutic intervention. While endovascular therapy is the preferred treatment approach, we describe a case where surgical embolectomy is an alternative approach in specific scenarios. In our case, we presented a patient with simultaneous PCD and acute limb ischemia (ALI).

Case report

A patient presented with haematuria, abdominal pain, cyanotic changes in the limb, and sensory/motor deficits in the right lower limb. Imaging tests revealed thromboembolic occlusion of both the arterial and venous systems and a bleeding tumour in the pelvic region. Due to the rapid progression of symptoms, macroscopic haematuria with anaemia, renal failure, and the necessity for intervention in both the arterial and venous systems, we performed a successful simultaneous surgical embolectomy of the arterial and venous systems right lower limb, resulting in prompt symptom resolution.

Discussion

Phlegmasia cerulea dolens is a rare manifestation of massive iliofemoral deep vein thrombosis. Its pathophysiology can indirectly compromise arterial patency. Treatment options include endovascular therapy - catheter-directed thrombolysis (CDT), percutaneous mechanical thrombectomy (PMT) or surgical intervention. These options carry risks, including damage to the venous endothelium or periprocedural pulmonary embolism. This case report demonstrates a situation where surgical intervention was a viable option. We presented a more endothelium-sparing surgical approach using a sterile compression bandage during embolectomy.

In conclusion

To date, there are no established guidelines from professional societies regarding the treatment of PCD. The authors emphasize the need for an individualized approach to patients with PCD. They also highlight the importance of access to comprehensive treatment, including both endovascular and surgical methods.

Methods

work has been reported in line with SCARE criteria.
简介多发性深静脉血栓(PCD)是一种罕见的、危及生命和肢体的急性大面积深静脉血栓(DVT),需要紧急治疗干预。虽然血管内治疗是首选的治疗方法,但我们描述了一个病例,在特定情况下,外科栓子切除术是一种替代方法。在我们的病例中,我们介绍了一名同时患有 PCD 和急性肢体缺血(ALI)的患者:患者出现血尿、腹痛、肢体发绀、右下肢感觉/运动障碍。影像学检查显示动脉和静脉系统均有血栓栓塞,盆腔区域有出血肿瘤。由于症状进展迅速、大面积血尿伴贫血、肾功能衰竭,以及必须同时对动静脉系统进行干预,我们成功地同时对患者右下肢的动静脉系统进行了栓塞切除手术,从而迅速缓解了症状:讨论:腓肠肌栓塞是一种罕见的髂股深层静脉血栓形成的表现。其病理生理学可间接损害动脉的通畅性。治疗方法包括血管内治疗--导管引导溶栓(CDT)、经皮机械血栓切除术(PMT)或外科干预。这些方案都存在风险,包括对静脉内皮的损伤或围手术期肺栓塞。本病例报告展示了一种可行的手术干预方案。我们介绍了一种在栓子切除术中使用无菌加压绷带的更能保护内皮的手术方法:结论:迄今为止,专业学会尚未制定有关 PCD 治疗的指导方针。作者强调了对 PCD 患者采取个体化治疗方法的必要性。他们还强调了获得综合治疗(包括血管内治疗和外科治疗)的重要性。
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引用次数: 0
Giant benign mesenteric cysts (mesothelioma and lymphangioma): A report of two cases. 巨大良性肠系膜囊肿(间皮瘤和淋巴管瘤):两个病例的报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-12 DOI: 10.1016/j.ijscr.2024.110587
Jesús Eduardo Prior-Rosas, Brenda Mejía-Ruíz, Brenda Areli Magdaleno-Becerra, Chantal Guadalupe Nava-Tenorio, Sheila Marilyn Alonso-Domínguez, Gabriela Eugenia Botello-Ortiz

Introduction and importance: Mesenteric cysts are a rare group of intra-abdominal tumors located in the mesentery or omentum, most of this lesion are asymptomatically but occasionally presents with non-specific symptoms, which makes diagnosis difficult.

Case presentation: We present two cases of giant mesenteric cyst in our Institution, the first case is a women of 23 years with previous gynecologic surgery with chronic abdominal pain and large abdominal mass CT showed a giant intraabdominal 30 × 25 × 15 cm, the patient went to laparotomy and a large mesenteric tumor found. The Histopathology reported a Benign cyst mesothelioma (BCM). The second case is a 47 year male with intermittent abdominal pain and abdominal CT shows a 20x21x15 cm tumor. Laparotomy was performed. Histopathology reported a large lymphangioma.

Clinical discussion: BCM tumors are rare intrabdominal lesions often diagnosed in premenopausal women. Its etiopathogenesis is still unclear, associated risk factors are endometriosis, pelvic inflammatory disease and previous pelvic surgery. Lymphangiomas are an infrequent cyst tumors. It results from a failure in the evolutionary development of the lymphatic system, often localized in the head and neck and its localization in the abdomen is even rare. The definitive diagnosis is made by histopathology.

Conclusion: Mesenteric cysts diagnosis if often challenge due to nonspecific symptoms and significant overlap in imaging appearance between the different entities, its diagnosis should be in mind when encounter a cystic abdominal tumor, surgical complete removal of this tumors is the optimal treatment to prevent recurrence and complications.

导言和重要性:肠系膜囊肿是一类罕见的位于肠系膜或网膜的腹腔内肿瘤,这种病变大多无症状,但偶尔也会出现非特异性症状,这给诊断带来了困难:第一个病例是一名 23 岁女性,曾做过妇科手术,伴有慢性腹痛和巨大腹部肿块,CT 显示腹腔内有一个 30 × 25 × 15 厘米的巨大肿块。组织病理学报告为良性囊性间皮瘤(BCM)。第二个病例是一名 47 岁男性,间歇性腹痛,腹部 CT 显示肿瘤为 20x21x15 厘米。患者接受了腹腔镜手术。组织病理学报告为巨大淋巴管瘤:BCM肿瘤是一种罕见的腹腔内病变,通常在绝经前妇女中确诊。其发病机制尚不清楚,相关的危险因素包括子宫内膜异位症、盆腔炎和盆腔手术。淋巴管瘤是一种不常见的囊性肿瘤。淋巴管瘤是一种不常见的囊性肿瘤,是淋巴系统进化发育失败的结果,通常发生在头颈部,而发生在腹部的淋巴管瘤更是罕见。组织病理学可做出明确诊断:肠系膜囊肿的诊断常因症状无特异性和不同实体间影像学表现明显重叠而面临挑战,因此在遇到腹部囊性肿瘤时应注意其诊断,手术完全切除该肿瘤是防止复发和并发症的最佳治疗方法。
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引用次数: 0
Destombes-Rosai-Dorfman disease: A case series of nodular and extra nodular involvement. Destombes-Rosai-Dorfman病:结节和结节外受累病例系列。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-12 DOI: 10.1016/j.ijscr.2024.110589
Jihène Houas, Monia Ghammam, Heyfa BelHadj-Miled, Amal Kedissa, Mouna Bellakhdher, Mohamed Abdelkefi

Introduction and importance: Rosai-Dorfman disease (RDD) is a rare benign histiocytic proliferative disorder characterized by painless lymph node enlargement and extranodal involvement. This disease often presents diagnostic challenges due to its variable clinical manifestations and the need for histologic confirmation.

Case series presentation: This case series examines five patients diagnosed with Rosai-Dorfman disease who presented with a variety of clinical manifestations. Patients ranged in age from 21 to 72 years and presented with a variety of symptoms including cervical lymphadenopathy, mediastinal adenopathies, thyroid nodules, and nasal obstruction. Diagnoses were confirmed by histologic examination and immunostaining, primarily with anti-PS100 antibody. Treatments included surgery, corticosteroids, and laser resection, with most cases showing favorable outcomes and no recurrence at follow-ups ranging from one to five years.

Clinical discussion: The diverse presentations of RDD in this case series underscore the importance of considering this entity in the differential diagnosis of lymphadenopathy and other mass lesions. Histologic examination and immunostaining are critical for accurate diagnosis.

Conclusion: This case series aims to highlight the diverse presentations, diagnostic approaches, and treatment outcomes of patients with Rosai-Dorfman disease and to contribute to a better understanding of this rare condition.

导言和重要性:罗赛-多夫曼病(RDD)是一种罕见的良性组织细胞增生性疾病,以无痛性淋巴结肿大和结外受累为特征。由于该病的临床表现多变,且需要组织学确诊,因此常常给诊断带来挑战:本病例系列研究了五名被诊断为罗赛-多夫曼病的患者,他们的临床表现多种多样。患者年龄从 21 岁到 72 岁不等,表现出各种症状,包括颈淋巴结病、纵隔腺病、甲状腺结节和鼻塞。通过组织学检查和免疫染色(主要是抗PS100抗体)确诊。治疗方法包括手术、皮质类固醇激素和激光切除术,大多数病例疗效良好,随访一至五年无复发:临床讨论:本系列病例中 RDD 的表现多种多样,强调了在淋巴结病和其他肿块病变的鉴别诊断中考虑这一实体的重要性。组织学检查和免疫染色对准确诊断至关重要:本病例系列旨在强调罗赛-多夫曼病患者的不同表现、诊断方法和治疗结果,并有助于更好地了解这种罕见疾病。
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引用次数: 0
Corrigendum to "A rare case of teratoma in the right atrium: A case report study" [Int. J. Surg. Case Rep. 124 (2024) 110448]. 对 "一例罕见的右心房畸胎瘤:病例报告研究" [Int. J. Surg. Case Rep. 124 (2024) 110448]。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-11 DOI: 10.1016/j.ijscr.2024.110565
Ahmad Alkheder, Ibrahim Fathallah, Abd Alrhman Alajrd, Ahmed Al-Talep, Zeina Alsodi, Saleh Takkem
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引用次数: 0
Resection of a large anterior mediastinum myxoid liposarcoma via clamshell thoracotomy in a resource-limited setting: A rare case report and literature review 在资源有限的情况下,通过蛤壳式胸廓切开术切除巨大的前纵隔肌样脂肪肉瘤:罕见病例报告和文献综述。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-10 DOI: 10.1016/j.ijscr.2024.110582
Mekonnen Feyissa Senbu , Hiwot Tedessa Habtamu , Tekaleg Lemessa Kebede , Samson Bitew Wordofa , Lalisa Bedasa Ayana

Background

Mediastinal liposarcoma is an extremely rare malignant tumor of adipocytic differentiation, comprising less than 1 % of all liposarcomas. The majority occur in the lower extremities, with approximately 75 % of cases. Myxoid liposarcoma of the anterior mediastinum can present similarly to other thoracic pathologies.

Case presentation

We present the case of a 36-year-old female who presented with a 14-day history of worsening dyspnea at rest, along with swelling of the upper extremities and face. On examination, distended neck and anterior chest veins were observed. Imaging studies revealed a large anterior mediastinal mass causing extrinsic compression of adjacent structures and a mediastinal shift to the right. Following stabilization, the patient underwent successful surgical resection of the mass.

Discussion

Myxomatous liposarcoma is a very rare tumor located in the mediastinum that presents with symptoms resembling other lung diseases. Common complaints include chest pain, shortness of breath, and difficulty swallowing. Diagnosis is largely based on radiological imaging or histological examination after surgery. The primary treatment involves surgery and occasionally chemotherapy. Prompt diagnosis and timely treatment enhance the likelihood of positive outcomes for those affected.

Conclusion

This case underscores the importance of considering mediastinal liposarcoma in the differential diagnosis of patients presenting with chronic cough and unquantified weight loss, especially when symptoms escalate into conditions such as superior vena cava syndrome. Early detection and timely treatment are crucial for improving outcomes. This case contributes valuable insight, particularly relevant to managing complex tumors in resource-limited settings.
背景:纵隔脂肪肉瘤是一种极为罕见的脂肪细胞分化恶性肿瘤,占所有脂肪肉瘤的比例不到 1%。大多数病例发生在下肢,约占 75%。前纵隔肌样脂肪肉瘤的表现与其他胸部病变相似:本病例是一名 36 岁女性的病例,她因休息时呼吸困难加重、上肢和面部肿胀而就诊 14 天。检查时发现颈部和胸前静脉胀大。影像学检查显示,前纵隔有一个巨大肿块,导致邻近结构受到外力压迫,纵隔向右侧移位。病情稳定后,患者成功接受了肿块切除手术:肌瘤性脂肪肉瘤是一种非常罕见的位于纵隔的肿瘤,其症状与其他肺部疾病相似。常见症状包括胸痛、气短和吞咽困难。诊断主要依据放射成像或手术后的组织学检查。主要治疗方法包括手术和偶尔的化疗。迅速诊断和及时治疗可提高患者获得积极疗效的可能性:本病例强调了在对慢性咳嗽和不明原因体重减轻患者进行鉴别诊断时考虑纵隔脂肪肉瘤的重要性,尤其是当症状升级为上腔静脉综合征等情况时。早期发现和及时治疗对改善预后至关重要。本病例提供了宝贵的见解,尤其适用于在资源有限的环境中管理复杂的肿瘤。
{"title":"Resection of a large anterior mediastinum myxoid liposarcoma via clamshell thoracotomy in a resource-limited setting: A rare case report and literature review","authors":"Mekonnen Feyissa Senbu ,&nbsp;Hiwot Tedessa Habtamu ,&nbsp;Tekaleg Lemessa Kebede ,&nbsp;Samson Bitew Wordofa ,&nbsp;Lalisa Bedasa Ayana","doi":"10.1016/j.ijscr.2024.110582","DOIUrl":"10.1016/j.ijscr.2024.110582","url":null,"abstract":"<div><h3>Background</h3><div>Mediastinal liposarcoma is an extremely rare malignant tumor of adipocytic differentiation, comprising less than 1 % of all liposarcomas. The majority occur in the lower extremities, with approximately 75 % of cases. Myxoid liposarcoma of the anterior mediastinum can present similarly to other thoracic pathologies.</div></div><div><h3>Case presentation</h3><div>We present the case of a 36-year-old female who presented with a 14-day history of worsening dyspnea at rest, along with swelling of the upper extremities and face. On examination, distended neck and anterior chest veins were observed. Imaging studies revealed a large anterior mediastinal mass causing extrinsic compression of adjacent structures and a mediastinal shift to the right. Following stabilization, the patient underwent successful surgical resection of the mass.</div></div><div><h3>Discussion</h3><div>Myxomatous liposarcoma is a very rare tumor located in the mediastinum that presents with symptoms resembling other lung diseases. Common complaints include chest pain, shortness of breath, and difficulty swallowing. Diagnosis is largely based on radiological imaging or histological examination after surgery. The primary treatment involves surgery and occasionally chemotherapy. Prompt diagnosis and timely treatment enhance the likelihood of positive outcomes for those affected.</div></div><div><h3>Conclusion</h3><div>This case underscores the importance of considering mediastinal liposarcoma in the differential diagnosis of patients presenting with chronic cough and unquantified weight loss, especially when symptoms escalate into conditions such as superior vena cava syndrome. Early detection and timely treatment are crucial for improving outcomes. This case contributes valuable insight, particularly relevant to managing complex tumors in resource-limited settings.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110582"},"PeriodicalIF":0.6,"publicationDate":"2024-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142630595","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
Single-stage surgical management of simultaneous pulmonary and splenic hydatidosis: A rare case report 同时患有肺脾包虫病的单阶段手术治疗:罕见病例报告
IF 0.6 Q4 SURGERY Pub Date : 2024-11-10 DOI: 10.1016/j.ijscr.2024.110580
Houssem Messaoudi , Habib Bessrour , Mokhles Lajmi , Wafa Ragmoun , Islam Mejri , Saber Hachicha

Introduction

hydatid disease, caused by Echinococcus granulosus, primarily affects the liver and lungs, with splenic involvement being exceedingly rare, occurring in only 0.5 % of cases. This case report highlights a 17-year-old male presenting with a complicated hydatid cyst in the lung, along with an incidental splenic cyst, emphasizing the importance of single-stage surgery in treating multi-organ hydatid disease.

Case presentation

a 17-year-old male presented with a three-month history of left-sided chest pain and a dry cough. Imaging revealed a complicated hydatid cyst in the left lung and an incidental splenic cyst. Serological tests confirmed the presence of anti-hydatid antibodies. A single-stage surgical approach was performed via a transthoracic route, involving cystectomy and pericystectomy for the pulmonary cyst, followed by removal of the splenic cyst. The postoperative recovery was uneventful, and the patient was discharged on the fifth day with a six-month course of oral albendazole.

Discussion

hydatid disease is a significant public health issue, with simultaneous pulmonary and splenic involvement being rare. Surgical intervention remains the cornerstone of treatment for pulmonary hydatid disease, with medical therapy used as an adjunct. In this case, a single-stage surgery was chosen due to its advantages, such as reduced anesthesia, shorter hospital stays, and faster recovery.

Conclusion

single-stage surgery provides an effective and efficient option for managing multi-organ hydatid disease. This case highlights its feasibility and benefits, particularly in young patients from endemic regions.
导言:由棘球蚴引起的包虫病主要影响肝脏和肺部,脾脏受累极为罕见,仅占病例的 0.5%。本病例报告重点介绍了一名 17 岁男性的肺部并发包虫囊肿以及偶发脾囊肿的病例,强调了单阶段手术治疗多器官包虫病的重要性。影像学检查发现左肺有一个复杂的包虫囊肿,并偶见脾脏囊肿。血清学检测证实存在抗水囊虫抗体。通过经胸途径进行了单阶段手术,包括肺囊肿的囊肿切除术和周围囊肿切除术,随后切除了脾囊肿。术后恢复顺利,患者在口服阿苯达唑六个月后于第五天出院。讨论:包虫病是一个重要的公共卫生问题,同时累及肺部和脾脏的情况很少见。手术干预仍是治疗肺包虫病的基石,药物治疗则是辅助手段。在本病例中,由于单阶段手术具有麻醉少、住院时间短、恢复快等优点,因此选择了单阶段手术。结论:单阶段手术为治疗多器官包虫病提供了有效和高效的选择,本病例凸显了其可行性和优势,特别是对于来自流行地区的年轻患者。
{"title":"Single-stage surgical management of simultaneous pulmonary and splenic hydatidosis: A rare case report","authors":"Houssem Messaoudi ,&nbsp;Habib Bessrour ,&nbsp;Mokhles Lajmi ,&nbsp;Wafa Ragmoun ,&nbsp;Islam Mejri ,&nbsp;Saber Hachicha","doi":"10.1016/j.ijscr.2024.110580","DOIUrl":"10.1016/j.ijscr.2024.110580","url":null,"abstract":"<div><h3>Introduction</h3><div>hydatid disease, caused by <em>Echinococcus granulosus</em>, primarily affects the liver and lungs, with splenic involvement being exceedingly rare, occurring in only 0.5 % of cases. This case report highlights a 17-year-old male presenting with a complicated hydatid cyst in the lung, along with an incidental splenic cyst, emphasizing the importance of single-stage surgery in treating multi-organ hydatid disease.</div></div><div><h3>Case presentation</h3><div>a 17-year-old male presented with a three-month history of left-sided chest pain and a dry cough. Imaging revealed a complicated hydatid cyst in the left lung and an incidental splenic cyst. Serological tests confirmed the presence of anti-hydatid antibodies. A single-stage surgical approach was performed via a transthoracic route, involving cystectomy and pericystectomy for the pulmonary cyst, followed by removal of the splenic cyst. The postoperative recovery was uneventful, and the patient was discharged on the fifth day with a six-month course of oral albendazole.</div></div><div><h3>Discussion</h3><div>hydatid disease is a significant public health issue, with simultaneous pulmonary and splenic involvement being rare. Surgical intervention remains the cornerstone of treatment for pulmonary hydatid disease, with medical therapy used as an adjunct. In this case, a single-stage surgery was chosen due to its advantages, such as reduced anesthesia, shorter hospital stays, and faster recovery.</div></div><div><h3>Conclusion</h3><div>single-stage surgery provides an effective and efficient option for managing multi-organ hydatid disease. This case highlights its feasibility and benefits, particularly in young patients from endemic regions.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110580"},"PeriodicalIF":0.6,"publicationDate":"2024-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142639807","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
The management of colo-colic intussusception on left colon tumor in an adult: Case presentation and review of the literature. 成人左结肠肿瘤结肠-结肠肠套叠的处理:病例介绍和文献综述。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-10 DOI: 10.1016/j.ijscr.2024.110578
Ali Kada, Hamza Sekkat, Mahdi Bahij, Mohammed Raiss, Farid Sabbah, Abdelmalek Hrora

Introduction and importance: Intestinal intussusception is rare in adults and often associated with underlying malignancies. In this case, a colo-colic intussusception involving the descending colon caused acute obstruction, ischemic pain, and carried a high risk for peritonitis, necessitating urgent surgical intervention to prevent severe complications.

Case presentation: We report the case of a 50-year-old male who presented with acute abdominal obtruction and a three-day history of fecal vomiting, left-sided abdominal pain, and recent rectal bleeding. Imaging revealed colo-colic intussusception of the descending colon due to a colonic tumor. Immediate surgical intervention was performed with an oncologic resection of the invaginated segment, including a left hemicolectomy with lymph node dissection. A diversionary left iliac colostomy was conducted, ensuring clear resection margins and reducing the risk of postoperative complications.

Clinical discussion: Intussusception in adults, while rare, frequently indicates a malignant etiology, and prompt diagnosis and management are essential. In this case, rapid surgical intervention allowed successful removal of the tumor with favorable oncologic outcomes and no recurrence at two-year follow-up. This case highlights the complexity of diagnosing intussusception in adults, where symptoms may mimic other gastrointestinal conditions and are often nonspecific.

Conclusion: This case underscores the critical importance of early detection and intervention for intussusception in adults. Awareness among physicians should be heightened to consider intussusception in adult patients presenting with symptoms such as ischemic pain or a palpable mass with associated pain, as timely intervention can lead to improved outcomes and reduce morbidity.

导言和重要性:肠套叠在成人中很少见,通常与潜在的恶性肿瘤有关。在本病例中,结肠-结肠肠套叠累及降结肠,导致急性梗阻、缺血性疼痛,并有腹膜炎的高风险,因此需要紧急手术治疗,以防止严重并发症的发生:我们报告了一例 50 岁男性的病例,他出现急性腹部梗阻,并有三天的大便呕吐、左侧腹痛和近期直肠出血病史。影像学检查显示,由于结肠肿瘤,降结肠出现结肠-结肠肠套叠。立即进行了手术治疗,对内陷部分进行了肿瘤切除,包括左半结肠切除术和淋巴结清扫术。进行了转移性左髂结肠造口术,确保了切除边缘清晰,降低了术后并发症的风险:临床讨论:成人肠套叠虽然罕见,但往往预示着恶性病因,因此及时诊断和治疗至关重要。在本病例中,快速的手术干预使肿瘤得以成功切除,并取得了良好的肿瘤治疗效果,随访两年未见复发。本病例凸显了成人肠套叠诊断的复杂性,因为成人肠套叠的症状可能与其他胃肠道疾病相似,而且往往没有特异性:本病例强调了早期发现和干预成人肠套叠的重要性。应提高医生的认识,在成人患者出现缺血性疼痛或可触及肿块并伴有疼痛等症状时,应考虑肠套叠,因为及时干预可改善预后并降低发病率。
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引用次数: 0
Rathke's cleft cyst apoplexy presented as pituitary apoplexy: A case report 拉斯克裂囊肿脑垂体骤停:病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-09 DOI: 10.1016/j.ijscr.2024.110571
Soumya Pahari , Yugant Khand , Stuti Yadav , Paawan Bahadur Bhandari , Purushottam Baniya , Nishan Bhandari

Introduction and importance

Rathke's cleft cyst (RCC) are non-malignant lesions arising from remnants of Rathke's pouch in the pituitary gland. Apoplexy is seen commonly in pituitary macroadenomas but very rarely in RCCs.

Case presentation

A 30-year-old male presented with a severe headache and vomiting. Imaging revealed an enlarged pituitary gland with possible hemorrhage in a RCC. The cyst was evacuated with endonasal transsphenoidal surgery, and histology confirmed RCC. Follow-up imaging showed complete cyst resolution, although he required levothyroxine for hypothyroidism.

Clinical discussion

The occurrence of hemorrhage within RCCs, although rare, mimics pituitary tumor apoplexy often complicating the diagnosis. The management is similar to pituitary tumor apoplexy, primarily involving surgical intervention. Postoperative care may require long-term hormonal replacement therapy in a significant number of patients.

Conclusion

This report underscores the importance of considering RCC in the differential diagnoses of pituitary lesions with hemorrhage with promising surgical outcome.
导言和重要性:拉氏裂隙囊肿(RCC)是垂体中拉氏袋残留物引起的非恶性病变。垂体大腺瘤通常会出现脑溢血,但在 RCC 中却非常罕见:一名 30 岁的男性因剧烈头痛和呕吐就诊。影像学检查发现垂体肿大,RCC 可能存在出血。经鼻内镜手术切除囊肿,组织学检查证实为 RCC。随访造影显示囊肿完全消退,但他需要服用左甲状腺素治疗甲状腺功能减退症:临床讨论:RCC内出血虽然罕见,但与垂体瘤中风相似,往往会使诊断复杂化。处理方法与垂体瘤栓塞相似,主要涉及手术干预。大量患者术后可能需要长期激素替代治疗:本报告强调了在脑垂体病变伴出血的鉴别诊断中考虑 RCC 的重要性,手术效果良好。
{"title":"Rathke's cleft cyst apoplexy presented as pituitary apoplexy: A case report","authors":"Soumya Pahari ,&nbsp;Yugant Khand ,&nbsp;Stuti Yadav ,&nbsp;Paawan Bahadur Bhandari ,&nbsp;Purushottam Baniya ,&nbsp;Nishan Bhandari","doi":"10.1016/j.ijscr.2024.110571","DOIUrl":"10.1016/j.ijscr.2024.110571","url":null,"abstract":"<div><h3>Introduction and importance</h3><div>Rathke's cleft cyst (RCC) are non-malignant lesions arising from remnants of Rathke's pouch in the pituitary gland. Apoplexy is seen commonly in pituitary macroadenomas but very rarely in RCCs.</div></div><div><h3>Case presentation</h3><div>A 30-year-old male presented with a severe headache and vomiting. Imaging revealed an enlarged pituitary gland with possible hemorrhage in a RCC. The cyst was evacuated with endonasal transsphenoidal surgery, and histology confirmed RCC. Follow-up imaging showed complete cyst resolution, although he required levothyroxine for hypothyroidism.</div></div><div><h3>Clinical discussion</h3><div>The occurrence of hemorrhage within RCCs, although rare, mimics pituitary tumor apoplexy often complicating the diagnosis. The management is similar to pituitary tumor apoplexy, primarily involving surgical intervention. Postoperative care may require long-term hormonal replacement therapy in a significant number of patients.</div></div><div><h3>Conclusion</h3><div>This report underscores the importance of considering RCC in the differential diagnoses of pituitary lesions with hemorrhage with promising surgical outcome.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110571"},"PeriodicalIF":0.6,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142644990","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
EX vivo liver resection and auto transplantation for a giant hepatocellular carcinoma: A case report 巨型肝细胞癌的体外肝切除和自体移植:病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-09 DOI: 10.1016/j.ijscr.2024.110573
Noureen Kanwal , Jahanzaib Haider , Siraj Haider , Mohammad Iqbal , Kiran Amir , Faisal Saud Dar

Introduction and importance

The curative options for locally advanced hepatocellular carcinomas involving the vessels are very limited. Ex vivo liver resection and auto transplantation (ERAT) is a novel surgical method, which has been used in the management of such complex liver space occupying lesions, which are rendered conventionally unresectable. This technique involves a complete hepatectomy, extracorporeal hepatic resection on the backbench, and then reimplantation of the remnant hepatic parenchyma. George et al. (2019) [1] In literature, Ex vivo liver resection and auto transplantation (ERAT) has been utilized in the management of both benign and malignant liver lesions, including hepatocellular carcinoma (HCC), cholangiocarcinoma, hepatic metastases, hepatic alveolar echinococcosis, focal nodular hyperplasia and hemangioma. Zawistowski et al. (2020) [2].

Case presentation

We report this case of a 28 years old male with a giant hepatocellular carcinoma, that deemed unresectable as it was closely abutting all three hepatic veins. After appropriate preoperative surgical planning, he underwent ex vivo liver resection and autotransplantation (ERAT). Patient had gradual uneventful recovery and he was discharged home on 12th postoperative day.

Clinical discussion

A radical (R0) resection is the main goal of the ex vivo liver resection and autotransplantation (ERAT) procedure, which can be used for curative intent in patients with liver lesions that are conventionally inoperable. It allows for precise extracorporeal resection, maximizes the residual liver volume and increases the likelihood of obtaining negative margins. Furthermore, the bench surgery in ice bath makes it easier to reconstruct the vasculature without the pressure of time constraints in situ, unlike conventional surgery, which can take a long time when done in a bleeding operative field. Zawistowski et al. (2020) [2].

Conclusion

For patients with complex liver lesions believed to be incurable with conventional surgical methods, ex vivo liver resection and autotransplantation (ERAT) provides an alternative.
导言和重要性:对于涉及血管的局部晚期肝细胞癌,治疗方案非常有限。体外肝切除和自体移植(ERAT)是一种新颖的手术方法,已被用于治疗这种复杂的肝脏空间占位病变,传统方法无法切除。该技术包括全肝切除、体外肝切除和残余肝实质再植。George 等人(2019 年)[1] 在文献中,体外肝切除和自体移植(ERAT)已被用于治疗肝脏良性和恶性病变,包括肝细胞癌(HCC)、胆管癌、肝转移瘤、肝泡棘球蚴病、局灶性结节增生和血管瘤。Zawistowski 等人(2020 年)[2]:我们报告了一例 28 岁男性巨大肝细胞癌患者的病例,由于肝细胞癌与三条肝静脉紧密相连,因此无法切除。经过适当的术前手术规划,他接受了体外肝切除和自体移植(ERAT)手术。患者恢复顺利,术后第 12 天出院回家:根治性(R0)切除是体外肝脏切除和自体移植术(ERAT)的主要目标,它可用于治疗传统上无法手术的肝脏病变患者。它可以进行精确的体外切除,最大限度地增加残余肝脏体积,并增加获得阴性边缘的可能性。此外,在冰浴中进行的台式手术更容易在没有时间限制的压力下就地重建血管,而不像传统手术那样,在出血的手术区进行需要很长时间。Zawistowski 等人(2020 年)[2].结论:对于被认为无法通过传统手术方法治愈的复杂肝脏病变患者,体外肝脏切除和自体移植(ERAT)提供了一种替代方案。
{"title":"EX vivo liver resection and auto transplantation for a giant hepatocellular carcinoma: A case report","authors":"Noureen Kanwal ,&nbsp;Jahanzaib Haider ,&nbsp;Siraj Haider ,&nbsp;Mohammad Iqbal ,&nbsp;Kiran Amir ,&nbsp;Faisal Saud Dar","doi":"10.1016/j.ijscr.2024.110573","DOIUrl":"10.1016/j.ijscr.2024.110573","url":null,"abstract":"<div><h3>Introduction and importance</h3><div>The curative options for locally advanced hepatocellular carcinomas involving the vessels are very limited. Ex vivo liver resection and auto transplantation (ERAT) is a novel surgical method, which has been used in the management of such complex liver space occupying lesions, which are rendered conventionally unresectable. This technique involves a complete hepatectomy, extracorporeal hepatic resection on the backbench, and then reimplantation of the remnant hepatic parenchyma. George et al. (2019) [<span><span>1</span></span>] In literature, Ex vivo liver resection and auto transplantation (ERAT) has been utilized in the management of both benign and malignant liver lesions, including hepatocellular carcinoma (HCC), cholangiocarcinoma, hepatic metastases, hepatic alveolar echinococcosis, focal nodular hyperplasia and hemangioma. Zawistowski et al. (2020) [<span><span>2</span></span>].</div></div><div><h3>Case presentation</h3><div>We report this case of a 28 years old male with a giant hepatocellular carcinoma, that deemed unresectable as it was closely abutting all three hepatic veins. After appropriate preoperative surgical planning, he underwent ex vivo liver resection and autotransplantation (ERAT). Patient had gradual uneventful recovery and he was discharged home on 12th postoperative day.</div></div><div><h3>Clinical discussion</h3><div>A radical (R0) resection is the main goal of the ex vivo liver resection and autotransplantation (ERAT) procedure, which can be used for curative intent in patients with liver lesions that are conventionally inoperable. It allows for precise extracorporeal resection, maximizes the residual liver volume and increases the likelihood of obtaining negative margins. Furthermore, the bench surgery in ice bath makes it easier to reconstruct the vasculature without the pressure of time constraints in situ, unlike conventional surgery, which can take a long time when done in a bleeding operative field. Zawistowski et al. (2020) [<span><span>2</span></span>].</div></div><div><h3>Conclusion</h3><div>For patients with complex liver lesions believed to be incurable with conventional surgical methods, ex vivo liver resection and autotransplantation (ERAT) provides an alternative.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"125 ","pages":"Article 110573"},"PeriodicalIF":0.6,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142630352","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}
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International Journal of Surgery Case Reports
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