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一例表现为后纵隔肿块的巨大胃胃肠道间质瘤。

A giant gastrointestinal stromal tumor of the stomach presenting as a posterior mediastinal mass.

作者信息

Chen Huijiao, Yao Jin, Tang Yuan, Zhang Hongying

机构信息

Department of Pathology, West China Hospital, Sichuan University Chengdu 610041, Sichuan, China.

Department of Radiology, West China Hospital, Sichuan University Chengdu 610041, Sichuan, China.

出版信息

Int J Clin Exp Pathol. 2017 Aug 1;10(8):8741-8745. eCollection 2017.

Abstract

Gastrointestinal stromal tumors (GISTs) involving thoracic region are very rare, most of which are esophageal in origin. Herein, we report a gastric GIST presenting as a posterior mediastinal mass, which provided diagnostic pitfalls due to its unusual anatomic location. The patient was a 68-year-old Chinese female, presenting with dysphagia, nausea and weight loss of 5 kg within 4 months. The contrast-enhanced thoracic computed tomography scan revealed a huge heterogeneous soft tissue mass in the posterior mediastinum. The core biopsy revealed a spindle cell tumor. The pathological features, in conjunction with the strong immunostaining pattern for CD117 and DOG-1 and the identification of exon 11 mutation, confirmed the diagnosis of GIST. The subsequent surgery revealed the tumor located entirely in the abdominal cavity, laying beneath the diaphragm, and pushing the diaphragm upward into the posterior mediastinum. To our best, there has been only one similar case reported in the English literature. As patients with GISTs either resectable or not may get potential benefits from imatinib currently, the identification of GIST is very important even before surgery. Clinicians and pathologists should keep in mind that GISTs involving thoracic region do exist. The morphological features, immunohistochemical panel including CD117 and DOG-1 and molecular genetic test, in combination with clinicopathological correlation are helpful in confirming the correct diagnosis.

摘要

累及胸部的胃肠道间质瘤(GISTs)非常罕见,其中大多数起源于食管。在此,我们报告一例表现为后纵隔肿块的胃GIST,因其不寻常的解剖位置给诊断带来了困难。患者为一名68岁的中国女性,出现吞咽困难、恶心,4个月内体重减轻5kg。胸部增强计算机断层扫描显示后纵隔有一个巨大的异质性软组织肿块。核心活检显示为梭形细胞瘤。病理特征,结合CD117和DOG-1的强免疫染色模式以及外显子11突变的鉴定,确诊为GIST。随后的手术显示肿瘤完全位于腹腔内,位于膈肌下方,并将膈肌向上推至后纵隔。据我们所知,英文文献中仅报道过一例类似病例。由于目前无论GIST患者是否可切除,都可能从伊马替尼中获益,因此即使在手术前识别GIST也非常重要。临床医生和病理学家应牢记,确实存在累及胸部的GIST。形态学特征、包括CD117和DOG-1的免疫组织化学检查以及分子遗传学检测,结合临床病理相关性有助于确诊。

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