Follicular Cholecystitis with Cholelithiasis: A Rare Case Report

M. Singh, I. Vishwakarma, J. Kumar, A. Omhare, V. Mishra, Yogita Verma
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引用次数: 6

Abstract

BackgroundFollicular hyperplasia of the gall bladder is an extremely rare and benign entity characterized by hyperplastic lymphoid follicle with germinal center consisting of the lymphoid population. MaterialsWe were reported a rare case of follicular hyperplasia of gall bladder in a 36 yr old female presented in the department of surgery with a right side upper abdomen pain, then she was diagnosed as cholecystitis and managed by cholecystectomy and specimen was received and processed for histopathological examination. ResultsDue to chronic cholecystitis patient present with right upper abdominal pain and upon histopathological examination diagnosed incidently as follicular cholecystitis. ConclusionHistopathological examination reveals a rare case of follicular cholecystitis. Key-wordsFollicular cholecystitis, Gall Bladder, Pseudolymphoma INTRODUCTION Gall Bladder diseases are a significant cause of morbidity and mortality. Diseases affecting the gall bladder comprise a wide spectrum of diseases including nonspecific inflammatory diseases, acute & chronic cholecystitis, granulomatous cholecystitis, follicular cholecystitis, gall bladder polyp, carcinoma pseudolymphoma. Follicular Cholecystitis is a condition in which there is a formation of numerous prominent lymphoid follicles in lamina propria throughout the gall bladder, creating a pseudolymphoma pattern. Follicle can be present throughout, the wall but most commonly seen in mucosal layer. Follicular cholecystitis constitutes less than 2% of cholecystectomies . This condition also occurs in lungs, orbit, skin and GIT. It has been mentioned in literature that lymphoid hyperplasia, pseudolymphoma and follicular cholecystitis are some of the terms which describes the same lesion of the gall bladder . We describe a rare case of follicular cholecystitis diagnosed incidently in 36 years old female in a routine cholecystectomy specimen. Access this article online Quick Response Code Website:
滤泡性胆囊炎合并胆石症1例报告
背景:胆囊滤泡增生是一种极其罕见的良性肿瘤,其特征是淋巴样滤泡增生,生发中心由淋巴样细胞组成。我们报告一例罕见的胆囊滤泡增生病例,患者36岁,女性,右侧上腹部疼痛,于外科就诊,诊断为胆囊炎,行胆囊切除术,取标本行组织病理学检查。结果慢性胆囊炎患者表现为右上腹部疼痛,经病理检查偶发为滤泡性胆囊炎。结论组织病理学检查发现一例罕见的滤泡性胆囊炎。关键词滤泡性胆囊炎,胆囊,假性淋巴瘤介绍胆囊疾病是发病率和死亡率的重要原因。影响胆囊的疾病包括多种疾病,包括非特异性炎症性疾病、急性和慢性胆囊炎、肉芽肿性胆囊炎、滤泡性胆囊炎、胆囊息肉、癌性假性淋巴瘤。滤泡性胆囊炎是指在整个胆囊固有层形成大量突出的淋巴样卵泡,形成假性淋巴瘤。滤泡可存在于整个细胞壁,但最常见于粘膜层。滤泡性胆囊炎占胆囊切除术的不到2%。这种情况也发生在肺、眼眶、皮肤和GIT。文献中提到,淋巴样增生、假性淋巴瘤和滤泡性胆囊炎是描述胆囊同一病变的一些术语。我们描述一个罕见的病例滤泡性胆囊炎偶然诊断在36岁的女性在常规胆囊切除术标本。在线阅读本文快速响应代码网站:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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