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IgG4相关性疾病表现为胃黏膜下肿瘤,经腹腔镜内镜联合手术切除:一例报告

IgG4-related disease presenting as a submucosal tumor of the stomach resected with laparoscopic endoscopic cooperative surgery: a case report.

作者信息

Yamane Taishi, Eto Kojiro, Morinaga Takeshi, Matsumura Kazuki, Yamashita Kohei, Tokunaga Ryuma, Harada Kazuto, Hiyoshi Yukiharu, Nagai Yohei, Iwatsuki Masaki, Iwagami Shiro, Miyamoto Yuji, Yoshida Naoya, Baba Hideo

机构信息

Department of Gastroenterological Surgery, Graduate School of Life Sciences, Kumamoto University, 1-1-1 Honjo, Kumamoto, 860-8556, Japan.

出版信息

Surg Case Rep. 2020 May 7;6(1):93. doi: 10.1186/s40792-020-00851-8.

Abstract

BACKGROUND

IgG4-related disease (IgG4-RD) is an immune-mediated disorder in which abundant IgG4-positive plasma cells infiltrate affected organs. There have been reported four cases of probable IgG4-RD presenting as a submucosal tumor of the stomach. We herein report the first case of definite IgG4-RD presenting as a submucosal tumor of the stomach resected with laparoscopic endoscopic cooperative surgery (LECS).

CASE PRESENTATION

A 70-year-old woman with a 6-year history of autoimmune pancreatitis was referred to our department because a 15-mm submucosal tumor in the greater curvature of the lower part of the stomach had been identified via upper gastrointestinal endoscopy. Endoscopic ultrasonography showed a 10-mm low-echoic lesion derived from the submucosal layer of the stomach. A fine-needle aspiration biopsy was attempted, but the tumor was too hard for sampling. F-fluorodeoxyglucose (FDG) positron emission tomography showed an FDG uptake, suggesting a possibility of malignant disease. As the diagnosis could not be confirmed, LECS for both the diagnosis and curative treatment was performed. A histopathological examination showed a tumor with IgG4-positive lymphoplasmacytic infiltration and fibrosis. The ratio of IgG4+/IgG+ lymphoplasmacytic cells was > 80%. A laboratory examination showed elevation of the serum IgG4 levels preoperatively. Thus, the final diagnosis was IgG4-RD of the stomach. No recurrence was observed within 1 year after surgery.

CONCLUSIONS

We encountered a case of definite IgG4-RD presenting as a gastric SMT in which a correct diagnosis was achieved by a minimally invasive LECS technique. IgG4-RD may present as a gastric lesion and should be taken into consideration as a differential diagnosis.

摘要

背景

IgG4相关性疾病(IgG4-RD)是一种免疫介导的疾病,其中大量IgG4阳性浆细胞浸润受累器官。已有4例可能的IgG4-RD表现为胃黏膜下肿瘤的报道。我们在此报告首例经腹腔镜内镜联合手术(LECS)切除的确诊为IgG4-RD且表现为胃黏膜下肿瘤的病例。

病例介绍

一名有6年自身免疫性胰腺炎病史的70岁女性因上消化道内镜检查发现胃下部大弯处有一个15毫米的黏膜下肿瘤而转诊至我科。内镜超声显示一个源自胃黏膜下层的10毫米低回声病变。尝试进行细针穿刺活检,但肿瘤质地过硬无法取样。F-氟脱氧葡萄糖(FDG)正电子发射断层扫描显示有FDG摄取,提示可能为恶性疾病。由于无法确诊,遂进行LECS以明确诊断并进行根治性治疗。组织病理学检查显示肿瘤有IgG4阳性淋巴浆细胞浸润和纤维化。IgG4+/IgG+淋巴浆细胞的比例>80%。实验室检查显示术前血清IgG4水平升高。因此,最终诊断为胃IgG4-RD。术后1年内未观察到复发。

结论

我们遇到一例确诊为IgG4-RD且表现为胃黏膜下肿瘤的病例,通过微创LECS技术实现了正确诊断。IgG4-RD可能表现为胃部病变,应作为鉴别诊断予以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/166e/7206475/93223c0f82de/40792_2020_851_Fig1_HTML.jpg

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