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首页> 外文期刊>World Journal of Surgical Oncology >Porta hepatic schwannoma: case report and a 30-year review of the literature yielding 15 cases
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Porta hepatic schwannoma: case report and a 30-year review of the literature yielding 15 cases

机译:门肝性神经鞘瘤:病例报告和30年文献回顾,产生15例

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摘要

Background Schwannomas located in the periportal region are extremely rare. Only 14 cases have been reported in the medical literature worldwide. Cases of porta hepatic schwannomas reported in the literature worldwide were reviewed. As a result, it is very challenging for surgeons to make a preoperative diagnosis due to its rarity and nonspecific imaging manifestations. Case Presentation A 57-year-old Chinese female was admitted to our institution with complaint of upper abdominal distension and the abdominal CT in the local hospital revealed a hypodense mass in the porta hepatis. A fine needle aspiration (FNA) was made to confirm the diagnosis, but the result was just suggestive of spindle cell neoplasia. Eventually, the patient underwent surgery and postoperative pathology confirmed schwannoma in porta hepatis. The patient recovered uneventfully with no evidence of recurrence after a follow-up period of 41 months. Conclusions It is essential for the final diagnosis of porta hepatic schwannomas to combine histological examination with immunohistochemistry after surgery. The main treatment of porta hepatic schwannomas is complete excision with free margins and no lymph node dissection. In some cases, biliary reconstruction or the proper hepatic and the gastroduodenal artery resection was performed because the tumor was inseparably attached to the extrahepatic bile duct or the proper hepatic and the gastroduodenal artery. Malignant transformation of schwannomas is very rare and the overall prognosis is satisfactory.
机译:背景位于周围区域的神经鞘瘤极少见。全世界医学文献中仅报道了14例。回顾了全世界文献中报道的门肝性神经鞘瘤的病例。结果,由于其稀有性和非特异性的影像学表现,对外科医师进行术前诊断非常具有挑战性。病例介绍一名57岁的中国女性因上腹部胀大而入院,当地医院的腹部CT显示肝门有低密度肿块。进行了细针穿刺(FNA)确认诊断,但结果只是提示梭形细胞瘤样变。最终,患者接受了手术,术后病理证实肝门有神经鞘瘤。随访41个月后,患者恢复平稳,无复发迹象。结论术后结合组织学检查和免疫组化对门静脉肝神经鞘瘤的最终诊断至关重要。门肝性神经鞘瘤的主要治疗方法是完全切除,边缘自由,无淋巴结清扫。在某些情况下,由于肿瘤附着在肝外胆管或肝和十二指肠动脉上,因此需要进行胆道重建或肝和十二指肠动脉的适当切除。神经鞘瘤的恶性转化非常少见,总体预后令人满意。

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