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胃炎性肌纤维母细胞瘤与胃胃肠道间质瘤及肝海绵状血管瘤同时存在。

Synchronous gastric inflammatory myofibroblastic tumour with gastrointestinal stromal tumour of the stomach and hepatic syringious haemangioma.

作者信息

Papadopoulou D, Chatziralli Ip, Papadopoulos V, Filitantzi C, Demertzidis C

机构信息

General Hospital of Veroia, Veroia, Greece.

出版信息

J Surg Case Rep. 2012 Jan 1;2012(1):7. doi: 10.1093/jscr/2012.1.7.

Abstract

Inflammatory myofibroblastic tumour of the stomach is a very rare lesion. A case of a gastric inflammatory myofibroblastic tumour associated with gastrointestinal stromal tumour of the stomach and hepatic syringious haemangioma is described. We report an 80-year-old male who had an exophytic mass in the area of the pylorus and the duodenum, where hepatic cysts were found in the magnetic resonance (MRI) scan on examination of hypochromic microcytic anaemia, and prolapsus and torsion of the bulb of the stomach found during gastroscopy. During surgical excision of the exophytic mass, a gastrointestinal stromal tumour from the gastric fundus and a syringious haemangioma from the superior hepatic surface were resected. All tumours were treated successfully by surgical excision. The patient had an uneventful recovery. Neither recurrence nor metastasis was found after a 12-month follow-up. To our knowledge, this is the first time that such an association is reported in the literature.

摘要

胃炎性肌纤维母细胞瘤是一种非常罕见的病变。本文描述了一例与胃胃肠道间质瘤和肝脏海绵状血管瘤相关的胃炎性肌纤维母细胞瘤病例。我们报告了一名80岁男性,其在幽门和十二指肠区域有一个外生性肿块,在因低色素小细胞性贫血进行检查时,磁共振成像(MRI)扫描发现肝脏囊肿,胃镜检查发现胃球部脱垂和扭转。在对外生性肿块进行手术切除时,切除了来自胃底的胃肠道间质瘤和来自肝脏上表面的海绵状血管瘤。所有肿瘤均通过手术切除成功治疗。患者恢复顺利。随访12个月后未发现复发或转移。据我们所知,这是文献中首次报道这种关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccdb/3649450/ca20e1f64fcb/jscr-2012-1-7fig1.jpg

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