Suppr超能文献

表现为梗阻性黄疸的 Vater 壶腹恶性胃肠道间质瘤。

Malignant gastrointestinal stromal tumor of the ampulla of Vater presenting with obstructive jaundice.

作者信息

Filippou Dimitrios K, Pashalidis N, Skandalakis P, Rizos S

机构信息

First Department of General Surgery, Pireaus General Hospital "Tzaneio", Afentouli and Tzani str, Pireaus-Athens, Greece.

出版信息

J Postgrad Med. 2006 Jul-Sep;52(3):204-6.

Abstract

Malignant gastrointestinal stromal tumor (GIST) consists a rare neoplasm, developing in small intestine and stomach. The presenting manifastations include weakness, weight loss, nausea, melena and anaemia. The present case refers to a 65 years old female patient with a GIST of the ampulla of Vater presenting with obstructive jaundice. Diagnosis was achieved pre-operatively by biopsies collected through diagnostic ERCP. The tumour was locally excised, with preservation of the ampulla. The histological analysis suggested low grade GIST positive for both CD 117 (c-kit) and CD34. Two years after the surgery the patient remains free of disease. Malignant GIST of the ampulla of the Vater is extremely rare as only few similar cases have been described in the literature. This is the first time a GIST being presented as obstructive jaundice ever reported. Despite the unavailability of EUS-FNA, the diagnosis was set preoperatively and the tumor was resected.

摘要

恶性胃肠道间质瘤(GIST)是一种罕见的肿瘤,发生于小肠和胃。其临床表现包括乏力、体重减轻、恶心、黑便和贫血。本病例为一名65岁女性患者,患有 Vater壶腹胃肠道间质瘤并伴有梗阻性黄疸。术前通过诊断性内镜逆行胰胆管造影(ERCP)收集活检组织得以确诊。肿瘤在保留壶腹的情况下进行了局部切除。组织学分析显示为低级别胃肠道间质瘤,CD117(c-kit)和CD34均呈阳性。术后两年患者无疾病复发。Vater壶腹恶性胃肠道间质瘤极为罕见,因为文献中仅描述了少数类似病例。这是首次报道以梗阻性黄疸为表现的胃肠道间质瘤。尽管无法进行超声内镜引导下细针穿刺活检(EUS-FNA),但术前仍做出了诊断并切除了肿瘤。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验