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肝十二指肠韧带内的神经鞘瘤:一例报告及文献复习

Schwannoma in the hepatoduodenal ligament: A case report and literature review.

作者信息

Xu Shao-Yan, Sun Ke, Xie Hai-Yang, Zhou Lin, Zheng Shu-Sen, Wang Wei-Lin

机构信息

Shao-Yan Xu, Hai-Yang Xie, Lin Zhou, Shu-Sen Zheng, Wei-Lin Wang, Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, Zhejiang Province, China.

出版信息

World J Gastroenterol. 2016 Dec 14;22(46):10260-10266. doi: 10.3748/wjg.v22.i46.10260.

Abstract

Schwannomas are mesenchymal neoplasms with low malignant potential that arise from Schwann cells. They can occur almost anywhere, although the most common locations are the head, neck and extremities. Primary benign schwannoma of the hepatoduodenal ligament is rare. To date, only three cases have been reported in the English literature. In the present study, we report a case of hepatoduodenal ligament schwannoma in a 43-year-old male, who was admitted to our hospital because of a abdominal mass found by physical examination. It was hard to determine the definitive location and diagnosis of the mass using ultrasound, computed tomography and magnetic resonance cholangiopancreatography. During laparotomy, the mass was found in the hepatoduodenal ligament and close to the cholecystic duct, so we resected the gallbladder and cholecystic duct along with the mass. The gross specimen revealed an 8.5 cm × 5.5 cm × 3.0 cm localized tumor. Microscopic examination showed that the tumor was mainly composed of spindle-shaped cells. Immunohistochemical staining showed a strong positive S-100 protein reaction. Finally, the lesion was diagnosed as a benign schwannoma in the hepatoduodenal ligament. However, one month later, the patient was readmitted to our hospital because of skin and sclera jaundice caused by common bile duct stenosis without common bile duct stone or tumor. The patient recovered well after implantation of a common bile duct stent under endoscopic retrograde cholangiopancreatography. He was followed up for a period of 17 mo, during which he was well with no complications.

摘要

施万细胞瘤是一种间叶性肿瘤,恶性潜能低,起源于施万细胞。它们几乎可发生于任何部位,不过最常见的部位是头、颈和四肢。肝十二指肠韧带原发性良性施万细胞瘤很罕见。迄今为止,英文文献中仅报道了3例。在本研究中,我们报告了1例43岁男性的肝十二指肠韧带施万细胞瘤,该患者因体格检查发现腹部肿块而入院。使用超声、计算机断层扫描和磁共振胰胆管造影很难确定肿块的确切位置和诊断。在剖腹手术中,发现肿块位于肝十二指肠韧带且靠近胆囊管,因此我们连同肿块一起切除了胆囊和胆囊管。大体标本显示一个8.5 cm×5.5 cm×3.0 cm的局限性肿瘤。显微镜检查显示肿瘤主要由梭形细胞组成。免疫组织化学染色显示S-100蛋白反应呈强阳性。最后,该病变被诊断为肝十二指肠韧带良性施万细胞瘤。然而,1个月后,患者因胆总管狭窄导致皮肤和巩膜黄疸再次入院,胆总管无结石或肿瘤。在内镜逆行胰胆管造影下植入胆总管支架后,患者恢复良好。对其进行了17个月的随访,在此期间他情况良好,无并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cea/5155187/cd0c8673440a/WJG-22-10260-g001.jpg

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