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Simultaneous intracranial acute and chronic subdural hematoma on one side: A rare case report. 一侧同时出现颅内急性和慢性硬膜下血肿:罕见病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-11 DOI: 10.1016/j.ijscr.2024.110436
Djoko Widodo, Mirza Ananda Pasaribu, Kevin Jonathan Sjukur, Husni Harmansyah, Muhammad Faruk

Introduction: While acute and chronic subdural hematomas (SDH) are relatively common, co-occurrence is rare. Here, we report a case of unilateral simultaneous acute and chronic SDH.

Case presentation: A 74-year-old man with comorbid diabetes mellitus and hypertension presented with decreased consciousness (Glasgow Coma Scale (GCS) 4; E1M2V1) with stable hemodynamics. Isochoric pupils and right motoric lateralization were found upon neurological examination. CT scan of the brain without contrast showed acute and chronic SDH in the left frontotemporoparietal area with a midline shift 2 cm to the right. An evacuation craniectomy of the SDH was performed. Postoperative care included mechanical ventilation, monitoring, fluid balance maintenance, and medication. The patient showed improvement during follow-up and was weaned off mechanical ventilation on the 5th day after surgery.

Clinical discussion: SDH with a thickness of 10 mm or more and mass effect requires surgical management. Various techniques can be used for surgical evacuation. The prognosis of chronic SDH patients depends on their clinical condition when admitted, with early diagnosis and intervention resulting in improved prognosis.

Conclusion: This rare case highlights the significance of promptly recognizing and addressing symptoms such as headache and decreased consciousness, especially in older patients with underlying health conditions. Good prognosis is dependent on prompt evaluation, including a head CT scan for recurrent headaches, and immediate treatment when necessary.

导言:虽然急性和慢性硬膜下血肿(SDH)相对常见,但同时发生的情况却很少见。在此,我们报告了一例单侧同时出现急性和慢性硬膜下血肿的病例:一名 74 岁的男性,合并糖尿病和高血压,出现意识减退(格拉斯哥昏迷量表(GCS)4;E1M2V1),血流动力学稳定。神经系统检查发现瞳孔等大,右侧运动偏侧。无对比剂的脑部CT扫描显示,左侧额颞顶区存在急性和慢性SDH,中线向右偏移2厘米。手术对SDH进行了开颅切除。术后护理包括机械通气、监测、维持体液平衡和药物治疗。患者在随访期间病情有所好转,并于术后第 5 天脱离了机械通气:临床讨论:厚度大于或等于 10 毫米且有肿块效应的 SDH 需要手术治疗。手术排空可采用多种技术。慢性 SDH 患者的预后取决于入院时的临床状况,早期诊断和干预可改善预后:这一罕见病例凸显了及时发现并处理头痛和意识减退等症状的重要性,尤其是对于有潜在健康问题的老年患者。良好的预后取决于及时的评估,包括对反复发作的头痛进行头部 CT 扫描,并在必要时立即进行治疗。
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引用次数: 0
Successful endoscopic resection of a rare extension of peripheral giant cell granuloma into the infratemporal fossa via the maxillary sinus: A case report study. 通过内窥镜成功切除经上颌窦延伸至颞下窝的罕见周围巨细胞肉芽肿:病例报告研究。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-18 DOI: 10.1016/j.ijscr.2024.110475
Waddah Al-Saadie, Nour Raffoul, Karim Chahine

Introduction and significance: Peripheral giant cell granuloma (PGCG) is a benign reactive lesion commonly found in the mandible but rarely in the maxillary sinus and extending to the infratemporal fossa, which poses a major challenge in excision in this case. It can occasionally lead to bone erosion. Complete surgical excision is the primary treatment.

Case presentation: We present a rare case of PGCG in the maxillary sinus of a male patient following the extraction of the maxillary second molar, resulting in destruction of the bony margins. The patient underwent complete endoscopic resection with a flap to repair the bone loss in the maxilla.

Clinical discussion: Clinicians should be aware of this uncommon location of PGCG to ensure accurate diagnosis and appropriate treatment with minimal patient trauma and excellent outcomes.

Conclusion: Endoscopy is a highly effective method for removing PGCG located in the maxillary sinus and extending to the infratemporal fossa, even in cases of large size. It offers excellent results and provides good visualization of the maxillary sinus.

导言和意义:周围巨细胞肉芽肿(PGCG)是一种良性反应性病变,常见于下颌骨,但很少发生在上颌窦,也很少扩展到颞下窝,这给本病例的切除手术带来了很大挑战。它偶尔会导致骨侵蚀。完全手术切除是主要的治疗方法:我们介绍了一例罕见的男性患者上颌窦内的 PGCG 病例,患者在拔除上颌第二磨牙后,上颌窦内的 PGCG 导致骨边缘遭到破坏。患者接受了完整的内窥镜切除术,并用皮瓣修复了上颌骨的骨质缺损:临床讨论:临床医生应了解这种不常见的 PGCG 位置,以确保准确诊断和适当治疗,将患者创伤降到最低,取得良好疗效:结论:内窥镜检查是切除位于上颌窦并延伸至颞下窝的PGCG的一种高效方法,即使是体积较大的病例也不例外。内窥镜手术效果极佳,并能很好地观察上颌窦。
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引用次数: 0
Lung cancer associated with partial anomalous pulmonary venous connection in the non-resected lobe: A case report. 肺癌伴非切除肺叶部分异常肺静脉连接:病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-12 DOI: 10.1016/j.ijscr.2024.110454
Yuuki Matsui, Koji Takami

Introduction and importance: Partial anomalous pulmonary venous connection (PAPVC) is a relatively rare congenital vascular anomaly that complicates the surgical management of lung cancer and other lung lesions.

Case presentation: A 74-year-old woman underwent computed tomography (CT) during an episode of chest trauma. Chest CT showed a 24-mm ground glass opacity in the right lower lobe and a PAPVC in the right upper lobe. She was diagnosed with suspected stage IA1 lung cancer with clinical T1miN0M0 and was scheduled for surgery. Preoperative catheterization revealed a pulmonary to systemic flow ratio (Qp/Qs) of 0.98. Surgical repair of PAPVC is indicated when the patient is symptomatic and has a Qp/Qs of 1.5 to 2.0 or more. The patient was scheduled for right lower lobectomy. Although worsening of postoperative right heart strain was considered, the Qp/Qs results indicated that surgical repair of the PAPVC was unnecessary. The intraoperative circulatory dynamics remained stable, and a right lower lobectomy was performed. Her postoperative course was uneventful. There was no evidence of right heart failure or recurrence of lung cancer at the last follow-up examination 6 and 12 months after surgery.

Clinical discussion: If the PAPVC is in the non-resected lobe, preoperative assessment is really important, as major lung resection can increase shunt flow and cause right heart failure.

Conclusion: We believe that careful interpretation of CT images of all pulmonary veins before major lung resection while considering PAPVC is important for safe perioperative management and adequate evaluation of cardiac dynamics when PAPVC is present.

导言和重要性:部分异常肺静脉连接(PAPVC)是一种相对罕见的先天性血管异常,会使肺癌和其他肺部病变的手术治疗复杂化:一名 74 岁的妇女在一次胸部外伤中接受了计算机断层扫描(CT)检查。胸部 CT 显示右下叶有 24 毫米磨玻璃不透明,右上叶有 PAPVC。她被诊断为疑似肺癌 IA1 期,临床症状为 T1miN0M0,并被安排进行手术。术前导管检查显示肺血流与全身血流比率(Qp/Qs)为 0.98。当患者有症状且 Qp/Qs 为 1.5 至 2.0 或更高时,应进行 PAPVC 手术修复。患者被安排进行右下肺叶切除术。虽然考虑到术后右心负荷加重,但 Qp/Qs 结果显示没有必要对 PAPVC 进行手术修复。术中循环动力学保持稳定,于是进行了右下叶切除术。她的术后过程很顺利。在术后 6 个月和 12 个月的最后一次随访检查中,没有发现右心衰竭或肺癌复发的迹象:临床讨论:如果 PAPVC 位于未切除的肺叶,那么术前评估就非常重要,因为肺部大部切除会增加分流量,导致右心衰竭:我们认为,在考虑到 PAPVC 的情况下,在肺大部切除术前仔细解读所有肺静脉的 CT 图像对于围手术期的安全管理和充分评估 PAPVC 存在时的心脏动力学非常重要。
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引用次数: 0
Inflammatory myofibroblastic tumor: A rare cause of intestinal obstruction: Case report. 炎性肌纤维母细胞瘤:肠梗阻的罕见病因:病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-13 DOI: 10.1016/j.ijscr.2024.110438
Nargis Maqbool, Khawaja Mohammad Babar Pal, Zeeshan Uddin, Fatima Safdar

Introduction and importance: Inflammatory myofibroblastic tumor IMT1 is a rare neoplasm with diverse clinical presentations, needing histological confirmation for diagnosis. The tumor often mimics malignant conditions, making accurate diagnosis challenging.

Case presentation: We report a case of a 29-year-old male presenting with long standing recurrent abdominal pain, with more recent increasing frequency and associated weight loss. Imaging revealed a heterogenous soft tissue lesions causing mechanical small bowel obstruction, prompting surgical intervention. Histology analysis confirmed the diagnosis of IMT.

Clinical discussion: This case highlights the importance of considering IMT in the differential diagnosis of neoplastic mechanical small bowel obstruction, particularly in patients presenting with atypical symptoms and image findings. Despite its rarity, IMT should be considered, as it can present similarly to more common malignancies. Further research is warranted to unravel the pathogenesis and refine management strategies for this intriguing neoplasm.

Conclusion: IMT is a rare and intriguing neoplasm that presents significant diagnostic challenge. This case emphasize the need for thorough histological evaluation to confirm rhe diagnosis and guide appropriate management strategies.

导言和重要性:炎性肌纤维母细胞瘤IMT1是一种罕见肿瘤,临床表现多种多样,需要组织学确诊。该肿瘤常与恶性肿瘤相似,因此准确诊断具有挑战性:我们报告了一例 29 岁男性的病例,患者长期反复腹痛,最近腹痛频率增加,并伴有体重减轻。影像学检查发现,异质性软组织病变导致机械性小肠梗阻,因此进行了手术治疗。组织学分析证实了 IMT 的诊断:本病例强调了在肿瘤性机械性小肠梗阻的鉴别诊断中考虑到IMT的重要性,尤其是在出现不典型症状和影像检查结果的患者中。尽管IMT很罕见,但仍应考虑,因为它的表现可能与更常见的恶性肿瘤相似。我们有必要开展进一步的研究,以揭示其发病机制,并完善针对这种罕见肿瘤的治疗策略:IMT是一种罕见的肿瘤,诊断难度很大。本病例强调需要进行彻底的组织学评估,以确诊流变并指导适当的治疗策略。
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引用次数: 0
Lobular carcinoma metastasis to endometrial polyps: Insights from a case report and literature analysis. 转移至子宫内膜息肉的小叶癌:病例报告和文献分析的启示。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-16 DOI: 10.1016/j.ijscr.2024.110463
Abdelhamid Benlghazi, Hamza Messaoudi, Saad Benali, Imane Tazi, Moulay Mehdi Elhassani, Jaouad Kouach

Introduction and importance: Endometrial polyps are rare sites of metastatic breast carcinoma. Such cases have mainly been reported in tamoxifen-related polyps.

Case presentation: We describe the case of a 56-year-old woman with invasive lobular carcinoma who was experiencing vaginal bleeding. She underwent hysteroscopy with biopsy. Microscopic examination revealed an endometrial polyp with foci of adenocarcinoma. The morphological features of the tumor matched those of the original breast carcinoma.

Clinical discussion: Neoplasms originating from extra-genital sites frequently spread to the female genital organs. However, these metastases are mainly concentrated in the ovaries and vagina, while those affecting the uterus are rare. Among non-genital malignant tumors, mammary carcinoma - particularly the lobular type - is the most common to affect the uterus, followed by digestive and pulmonary tumors. Metastases within an endometrial polyp are particularly unusual.

Conclusions: It is crucial to consider metastatic tumors when assessing vaginal bleeding in patients with breast carcinoma. Because of the possibility of endometrial polyps being affected by metastasis, pathologists must examine them rigorously and thoroughly.

导言和重要性:子宫内膜息肉是转移性乳腺癌的罕见部位。此类病例主要见于他莫昔芬相关息肉:我们描述了一名 56 岁女性的病例,她患有浸润性小叶癌,并伴有阴道出血。她接受了宫腔镜检查和活组织检查。显微镜检查发现子宫内膜息肉伴有腺癌病灶。肿瘤的形态特征与原发乳腺癌相符:临床讨论:源于生殖器外部位的肿瘤经常会转移到女性生殖器官。然而,这些转移主要集中在卵巢和阴道,而影响子宫的转移则很少见。在非生殖器恶性肿瘤中,乳腺癌--尤其是小叶型乳腺癌--是最常见的影响子宫的肿瘤,其次是消化系统肿瘤和肺部肿瘤。子宫内膜息肉的转移尤为罕见:结论:在评估乳腺癌患者阴道出血时,考虑转移性肿瘤至关重要。由于子宫内膜息肉有可能发生转移,病理学家必须对其进行严格、彻底的检查。
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引用次数: 0
Surgical resection of a metastatic para-aortic lymph node deposit of renal mucinous tubular and spindle cell carcinoma - A case report. 肾粘液性管状细胞癌和纺锤形细胞癌转移性主动脉旁淋巴结沉积的手术切除--病例报告。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-21 DOI: 10.1016/j.ijscr.2024.110494
S M Norton, E Browne, E Low, D O'Connor, R Shatwan, C M Dowling

Introduction and importance: Mucinous tubular and spindle cell carcinoma (MTSCC) is a rare and usually slow-growing subtype of renal cell carcinoma (RCC), with low malignant potential. There is scant knowledge in the literature of this rare subtype of renal cell carcinoma.

Case presentation: We present the case of a 56 year old with an aggressive recurrent metastatic MTSCC para-aortic lymph node treated with surgical excision.

Clinical discussion: This case is unusual due to its recurrent and aggressive metastatic nature and not typical for this rare subtype of renal cell carcinoma.

Conclusion: Metastatic and recurrent renal mucinous tubular and spindle cell carcinoma is a very rare entity. Our case report aims to add to the limited knowledge in the literature on this rare malignancy.

导言和重要性:粘液性肾小管和纺锤形细胞癌(MTSCC)是肾细胞癌(RCC)的一种罕见亚型,通常生长缓慢,恶性程度低。关于这种罕见亚型肾细胞癌的文献资料很少:临床讨论:本例患者 56 岁,患有侵袭性复发性转移性 MTSCC,主动脉旁淋巴结经手术切除治疗:临床讨论:该病例因其复发和侵袭性转移性质而不同寻常,在这种罕见亚型肾细胞癌中并不典型:结论:转移性和复发性肾粘液管癌和纺锤形细胞癌是一种非常罕见的实体肿瘤。我们的病例报告旨在补充文献中关于这种罕见恶性肿瘤的有限知识。
{"title":"Surgical resection of a metastatic para-aortic lymph node deposit of renal mucinous tubular and spindle cell carcinoma - A case report.","authors":"S M Norton, E Browne, E Low, D O'Connor, R Shatwan, C M Dowling","doi":"10.1016/j.ijscr.2024.110494","DOIUrl":"10.1016/j.ijscr.2024.110494","url":null,"abstract":"<p><strong>Introduction and importance: </strong>Mucinous tubular and spindle cell carcinoma (MTSCC) is a rare and usually slow-growing subtype of renal cell carcinoma (RCC), with low malignant potential. There is scant knowledge in the literature of this rare subtype of renal cell carcinoma.</p><p><strong>Case presentation: </strong>We present the case of a 56 year old with an aggressive recurrent metastatic MTSCC para-aortic lymph node treated with surgical excision.</p><p><strong>Clinical discussion: </strong>This case is unusual due to its recurrent and aggressive metastatic nature and not typical for this rare subtype of renal cell carcinoma.</p><p><strong>Conclusion: </strong>Metastatic and recurrent renal mucinous tubular and spindle cell carcinoma is a very rare entity. Our case report aims to add to the limited knowledge in the literature on this rare malignancy.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11532900/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142510521","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
Clinicopathological characterization of tall cell carcinoma with reversed polarity of the breast: A case report and review of the litterature. 乳腺极性颠倒的高细胞癌的临床病理特征:病例报告和文献综述。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-13 DOI: 10.1016/j.ijscr.2024.110444
Ines Houissa, Yoldez Houcine, Amira Hmidi, Hanène Bouaziz, Tarek Dieb, Maha Driss

Introduction: Tall cell carcinoma of the breast with reverse polarity (TCCRP) is a recently described rare entity with low potential for malignancy which exhibits morphological features with tall cell variant of papillary thyroid carcinoma. Immunohistochemical and molecular studies help establish the diagnosis.

Case report: We report the case of a 45-year-old woman with no significant medical or surgical history who presented with mastodynia. Physical examination was negative. Screening by bilateral mammography revealed a mass of the right breast which was classified as 4B. The mass was surgically excised. The pathological report concluded to a TCCRP of the breast with free margins. The tumor cells were negative for hormone receptors as well as for the Human Epidermal Growth Factor Receptor-2 (HER2neu). The patient underwent a sentinel lymph node dissection that was negative followed by loco-regional radiotherapy. Chemotherapy and endocrine therapy were not indicated for the patient. After 24 months of follow-up, no signs of loco-regional or distant recurrences have been identified.

Clinical discussion: TCCRP is a rare entity that has been recently introduced in the WHO classification of breast cancer. It is usually a triple negative tumor, negative to TTF1 and thyroglobulin with low proliferation index, and a low potential for malignancy. Wide excision is the keystone of the treatment; however, chemotherapy and radiotherapy are still controversial due to lack of evidence.

Conclusion: TCCRP is a rare entity, which carries an excellent prognosis. A proper diagnosis is essential to conduct the best treatment next to a careful follow-up due to the ambiguous natural history of this rare entity.

Papers that have been previously published as meeting abstracts: None.

导言:具有反向极性的乳腺高细胞癌(TCCRP)是最近描述的一种罕见病例,其恶性可能性较低,具有甲状腺乳头状癌高细胞变异的形态学特征。免疫组化和分子研究有助于确诊:我们报告了一例 45 岁女性的病例,她没有明显的内外科病史,却出现了乳房胀痛。体格检查呈阴性。双侧乳房 X 光检查发现右侧乳房有一肿块,被列为 4B。手术切除了肿块。病理报告结果为乳腺 TCCRP,边缘游离。肿瘤细胞的激素受体和人类表皮生长因子受体-2(HER2neu)均为阴性。患者接受了前哨淋巴结清扫术,结果为阴性,随后接受了局部区域放疗。化疗和内分泌治疗不适用于该患者。经过24个月的随访,没有发现局部或远处复发的迹象:临床讨论:TCCRP是一种罕见的肿瘤,最近才被纳入世界卫生组织的乳腺癌分类中。它通常为三阴性肿瘤,TTF1和甲状腺球蛋白阴性,增殖指数低,恶性可能性小。广泛切除是治疗的关键,但由于缺乏证据,化疗和放疗仍存在争议:结论:TCCRP 是一种罕见病,预后良好。结论:TCCRP 是一种罕见疾病,预后极佳。由于这种罕见疾病的自然病史不明确,因此正确诊断是进行最佳治疗和仔细随访的关键:无。
{"title":"Clinicopathological characterization of tall cell carcinoma with reversed polarity of the breast: A case report and review of the litterature.","authors":"Ines Houissa, Yoldez Houcine, Amira Hmidi, Hanène Bouaziz, Tarek Dieb, Maha Driss","doi":"10.1016/j.ijscr.2024.110444","DOIUrl":"10.1016/j.ijscr.2024.110444","url":null,"abstract":"<p><strong>Introduction: </strong>Tall cell carcinoma of the breast with reverse polarity (TCCRP) is a recently described rare entity with low potential for malignancy which exhibits morphological features with tall cell variant of papillary thyroid carcinoma. Immunohistochemical and molecular studies help establish the diagnosis.</p><p><strong>Case report: </strong>We report the case of a 45-year-old woman with no significant medical or surgical history who presented with mastodynia. Physical examination was negative. Screening by bilateral mammography revealed a mass of the right breast which was classified as 4B. The mass was surgically excised. The pathological report concluded to a TCCRP of the breast with free margins. The tumor cells were negative for hormone receptors as well as for the Human Epidermal Growth Factor Receptor-2 (HER2neu). The patient underwent a sentinel lymph node dissection that was negative followed by loco-regional radiotherapy. Chemotherapy and endocrine therapy were not indicated for the patient. After 24 months of follow-up, no signs of loco-regional or distant recurrences have been identified.</p><p><strong>Clinical discussion: </strong>TCCRP is a rare entity that has been recently introduced in the WHO classification of breast cancer. It is usually a triple negative tumor, negative to TTF1 and thyroglobulin with low proliferation index, and a low potential for malignancy. Wide excision is the keystone of the treatment; however, chemotherapy and radiotherapy are still controversial due to lack of evidence.</p><p><strong>Conclusion: </strong>TCCRP is a rare entity, which carries an excellent prognosis. A proper diagnosis is essential to conduct the best treatment next to a careful follow-up due to the ambiguous natural history of this rare entity.</p><p><strong>Papers that have been previously published as meeting abstracts: </strong>None.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11539130/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142510511","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
Colpocephaly and corpus callosum dysgenesis in an adult: A rare case report. 一例罕见病例报告:罕见病例报告
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-19 DOI: 10.1016/j.ijscr.2024.110484
Soheil Mirzaei, Zahra Motaghed, Hooshmand Zarei

Introduction: Colpocephaly, a midline anomaly, may be associated with agenesis of the corpus callosum. While prenatal diagnosis is possible, this malformation is rarely detected in adults and may be asymptomatic.

Case presentation: We present a case of a 54-year-old male with Colpocephaly and dysgenesis of the corpus callosum, incidentally diagnosed during an emergency department visit. Computed tomography imaging revealed bilateral dilation of the posterior horns of the lateral ventricles and the absence of the corpus callosum.

Clinical discussion: Although some adults with Colpocephaly may show clinical symptoms, this anomaly can often be an incidental finding in asymptomatic individuals. Medical imaging plays a crucial role in the early diagnosis of this anomaly. Prenatal ultrasound can also detect midline anomalies, including Colpocephaly.

Conclusion: Awareness of this anomaly can prevent unnecessary diagnostic and therapeutic interventions.

简介无头畸形是一种中线畸形,可能与胼胝体发育不全有关。虽然可以进行产前诊断,但这种畸形在成人中很少被发现,而且可能没有症状:我们介绍了一例 54 岁男性的病例,他患有无脑畸形和胼胝体发育不良,是在急诊就诊时偶然被诊断出来的。计算机断层扫描成像显示双侧侧脑室后角扩张,胼胝体缺失:临床讨论:尽管一些患有无脑畸形的成年人可能会出现临床症状,但这种畸形往往是无症状者的偶然发现。医学影像在这种畸形的早期诊断中起着至关重要的作用。产前超声波检查也能发现中线畸形,包括脐带绕颈畸形:结论:对这种畸形的认识可以避免不必要的诊断和治疗干预。
{"title":"Colpocephaly and corpus callosum dysgenesis in an adult: A rare case report.","authors":"Soheil Mirzaei, Zahra Motaghed, Hooshmand Zarei","doi":"10.1016/j.ijscr.2024.110484","DOIUrl":"10.1016/j.ijscr.2024.110484","url":null,"abstract":"<p><strong>Introduction: </strong>Colpocephaly, a midline anomaly, may be associated with agenesis of the corpus callosum. While prenatal diagnosis is possible, this malformation is rarely detected in adults and may be asymptomatic.</p><p><strong>Case presentation: </strong>We present a case of a 54-year-old male with Colpocephaly and dysgenesis of the corpus callosum, incidentally diagnosed during an emergency department visit. Computed tomography imaging revealed bilateral dilation of the posterior horns of the lateral ventricles and the absence of the corpus callosum.</p><p><strong>Clinical discussion: </strong>Although some adults with Colpocephaly may show clinical symptoms, this anomaly can often be an incidental finding in asymptomatic individuals. Medical imaging plays a crucial role in the early diagnosis of this anomaly. Prenatal ultrasound can also detect midline anomalies, including Colpocephaly.</p><p><strong>Conclusion: </strong>Awareness of this anomaly can prevent unnecessary diagnostic and therapeutic interventions.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11539127/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142510512","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
A rare case of teratoma in the right atrium: A case report study. 右心房畸胎瘤的罕见病例:病例报告研究。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-12 DOI: 10.1016/j.ijscr.2024.110448
Ahmad Alkheder, Ibrahim Fathallah, Abd Alrhman Alajrd, Ahmed Al-Talep, Zeina Alsodi, Saleh Takkem

Introduction: Teratomas are neoplasms originating from embryonic tissues, characterized by a diverse composition of cells from all three germ layers in varying ratios. Rarely reported in the heart, we present here a rare case of a teratoma in the right atrium of a newborn.

Case presentation: A 20-h-old newborn was referred for a mild heart murmur. An echocardiogram revealed a 6 × 9 mm mass in the right atrium, attached to the interatrial septum. The mass caused mild tricuspid regurgitation without any significant pressure gradient. Surgery to remove the mass was successful. Pathological examination confirmed the mass as a teratoma. The child was discharged in excellent health and has had normal follow-up exams.

Discussion: Mature teratomas, a common type of germ cell tumor, are rare in the mediastinum, accounting for 10-15 % of mediastinal masses. These tumors arise from displaced primordial germ cells, which may become malignant. They can metastasize to the heart via various routes, causing symptoms like cough, dyspnea, and chest pain due to compression of mediastinal structures. Severe cases may lead to superior vena cava syndrome or hemoptysis. Tumor location influences clinical presentation, with some posing life-threatening risks.

Conclusion: Early diagnosis and intervention were crucial in preventing severe complications. This case emphasizes the importance of vigilant clinical evaluation and timely surgical management for infants presenting with cardiac symptoms.

导言:畸胎瘤是起源于胚胎组织的肿瘤,其特点是由来自三个胚层的不同比例的细胞组成。心脏畸胎瘤鲜有报道,我们在此介绍一例新生儿右心房畸胎瘤的罕见病例:一名 20 岁的新生儿因轻微心脏杂音而转诊。超声心动图显示,右心房有一个 6 × 9 毫米的肿块,与房间隔相连。肿块导致轻度三尖瓣反流,但没有明显的压力梯度。手术成功切除了肿块。病理检查证实肿块为畸胎瘤。患儿出院后健康状况良好,随访检查一切正常:讨论:成熟畸胎瘤是一种常见的生殖细胞瘤,在纵隔中很少见,占纵隔肿块的 10-15%。这些肿瘤源于移位的原始生殖细胞,可能会恶变。它们可通过各种途径转移到心脏,因压迫纵隔结构而引起咳嗽、呼吸困难和胸痛等症状。严重病例可能导致上腔静脉综合征或咯血。肿瘤位置会影响临床表现,有些肿瘤会危及生命:结论:早期诊断和干预对预防严重并发症至关重要。本病例强调了对出现心脏症状的婴儿进行警惕性临床评估和及时手术治疗的重要性。
{"title":"A rare case of teratoma in the right atrium: A case report study.","authors":"Ahmad Alkheder, Ibrahim Fathallah, Abd Alrhman Alajrd, Ahmed Al-Talep, Zeina Alsodi, Saleh Takkem","doi":"10.1016/j.ijscr.2024.110448","DOIUrl":"10.1016/j.ijscr.2024.110448","url":null,"abstract":"<p><strong>Introduction: </strong>Teratomas are neoplasms originating from embryonic tissues, characterized by a diverse composition of cells from all three germ layers in varying ratios. Rarely reported in the heart, we present here a rare case of a teratoma in the right atrium of a newborn.</p><p><strong>Case presentation: </strong>A 20-h-old newborn was referred for a mild heart murmur. An echocardiogram revealed a 6 × 9 mm mass in the right atrium, attached to the interatrial septum. The mass caused mild tricuspid regurgitation without any significant pressure gradient. Surgery to remove the mass was successful. Pathological examination confirmed the mass as a teratoma. The child was discharged in excellent health and has had normal follow-up exams.</p><p><strong>Discussion: </strong>Mature teratomas, a common type of germ cell tumor, are rare in the mediastinum, accounting for 10-15 % of mediastinal masses. These tumors arise from displaced primordial germ cells, which may become malignant. They can metastasize to the heart via various routes, causing symptoms like cough, dyspnea, and chest pain due to compression of mediastinal structures. Severe cases may lead to superior vena cava syndrome or hemoptysis. Tumor location influences clinical presentation, with some posing life-threatening risks.</p><p><strong>Conclusion: </strong>Early diagnosis and intervention were crucial in preventing severe complications. This case emphasizes the importance of vigilant clinical evaluation and timely surgical management for infants presenting with cardiac symptoms.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142477855","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Successful vaginal delivery in a patient with reconstructed bladder exstrophy and vaginoplasty after cesarean section, a case report from Syria. 来自叙利亚的病例报告:剖宫产术后膀胱外翻和阴道成形术重建患者成功阴道分娩。
IF 0.6 Q4 SURGERY Pub Date : 2024-11-01 Epub Date: 2024-10-12 DOI: 10.1016/j.ijscr.2024.110457
Maram Balouli, Omran Janoud, Aya Ahmad, Ahmad Mustafa Ahmad, Basel Ahmad, Bashar Kurdi

Introduction and importance: Bladder exstrophy (BE) is a rare congenital anomaly in which the anterior wall of the bladder is absent. In females, sexuality and fertility may be negatively affected with the association with pubic diastasis, dysplasia of the pelvic floor muscles, clitoris bifurcated, short vagina or narrow introitus.

Presentation of case: We present a case of 26-year-old woman with treated BE, vaginoplasty, and bicornuate uterus that came at week 36 of gestation. An elective cesarean section was made by paramedian section. Five years later, she came back with placental abruption at week 30 of gestation, and a successful vaginal delivery was made.

Discussion: Bladder exstrophy is a challenging disease that is accompanied with other morbidities. Impaired fertility is common due to previous surgeries and concomitant diseases, and pregnancy is high risk for both mother and baby. Delivery should be at a tertiary referral obstetric hospital.

Conclusion: Balancing the pros and cones of medical decision in order to achieve the best outcomes for both the mother and child is crucial, as choosing the right decision depends on the presentation and past history of the patient not only the existence of the bladder exstrophy.

导言和重要性:膀胱外翻(BE)是一种罕见的先天性畸形,即膀胱前壁缺失。在女性患者中,性能力和生育能力可能会受到负面影响,并伴有耻骨发育不良、盆底肌肉发育不良、阴蒂分叉、阴道短或阴道口狭窄等症状:我们介绍了一例 26 岁女性的病例,她在妊娠第 36 周时患有经治疗的 BE、阴道成形术和双角子宫。她选择了剖宫产术。五年后,她在妊娠第 30 周再次出现胎盘早剥,经阴道顺利分娩:讨论:膀胱萎缩是一种具有挑战性的疾病,并伴有其他疾病。讨论:膀胱外翻是一种具有挑战性的疾病,并伴有其他病症,由于之前的手术和并发症,生育能力受损很常见,妊娠对母亲和婴儿来说都是高风险。分娩应在三级转诊产科医院进行:平衡医疗决策的利弊,为母亲和孩子实现最佳治疗效果至关重要,因为选择正确的决策不仅取决于膀胱萎缩的存在,还取决于患者的表现和既往病史。
{"title":"Successful vaginal delivery in a patient with reconstructed bladder exstrophy and vaginoplasty after cesarean section, a case report from Syria.","authors":"Maram Balouli, Omran Janoud, Aya Ahmad, Ahmad Mustafa Ahmad, Basel Ahmad, Bashar Kurdi","doi":"10.1016/j.ijscr.2024.110457","DOIUrl":"10.1016/j.ijscr.2024.110457","url":null,"abstract":"<p><strong>Introduction and importance: </strong>Bladder exstrophy (BE) is a rare congenital anomaly in which the anterior wall of the bladder is absent. In females, sexuality and fertility may be negatively affected with the association with pubic diastasis, dysplasia of the pelvic floor muscles, clitoris bifurcated, short vagina or narrow introitus.</p><p><strong>Presentation of case: </strong>We present a case of 26-year-old woman with treated BE, vaginoplasty, and bicornuate uterus that came at week 36 of gestation. An elective cesarean section was made by paramedian section. Five years later, she came back with placental abruption at week 30 of gestation, and a successful vaginal delivery was made.</p><p><strong>Discussion: </strong>Bladder exstrophy is a challenging disease that is accompanied with other morbidities. Impaired fertility is common due to previous surgeries and concomitant diseases, and pregnancy is high risk for both mother and baby. Delivery should be at a tertiary referral obstetric hospital.</p><p><strong>Conclusion: </strong>Balancing the pros and cones of medical decision in order to achieve the best outcomes for both the mother and child is crucial, as choosing the right decision depends on the presentation and past history of the patient not only the existence of the bladder exstrophy.</p>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11532446/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142477865","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
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International Journal of Surgery Case Reports
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