Primary mucosa associated lymphoid tissue lymphoma of the gallbladder: A case report and review of literature.

IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Mi-Rin Lee, Kyu-Yun Jang, Jae-Do Yang
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引用次数: 0

Abstract

Background: The primary lymphomas of mucosa associated lymphoid tissue (MALT) of the gallbladder (GB) is an extremely rare of non-Hodgkin lymphoma. Many patients exhibit symptoms like gallstone disease, and in some cases, the lymphoma may be detected through imaging even without apparent symptoms. Only 19 cases of primary MALT lymphoma in the GB have been previously reported. Differential diagnosis from typical GB carcinoma based solely on imaging findings can be challenging, and definitive diagnosis often requires surgical intervention.

Case summary: We present a patient in an 82-year-old man who was initially diagnosed with prostate cancer but incidentally detected GB wall thickening from magnetic resonance imaging conducted for prostatic surgery and subsequent radical cholecystectomy revealed primary MALT lymphoma of the GB. The patient was followed up by a medical oncologist, and after discussion, the decision was made to continue observation with close monitoring without systemic chemotherapy given the asymptomatic presentation. The patient has been free of recurrence for 16 months after the surgery. Although precise diagnosis before the surgery was difficult in this case, preoperative examinations revealed a submucosal tumor-like lesion.

Conclusion: MALT lymphoma of GB remains little known in many previous studies. It is really difficult to preoperatively diagnose. The combination of clinical presentation, postoperative histology and immunohistochemistry contribute to diagnosis and carry out appropriate management.

原发性胆囊粘膜相关淋巴组织淋巴瘤1例报告及文献复习。
背景:原发性胆囊粘膜相关淋巴组织淋巴瘤(MALT)是一种极为罕见的非霍奇金淋巴瘤。许多患者表现出胆结石病等症状,在某些情况下,即使没有明显症状,也可以通过影像学发现淋巴瘤。在英国只有19例原发性MALT淋巴瘤被报道过。仅根据影像学表现与典型GB癌鉴别诊断具有挑战性,明确诊断通常需要手术干预。病例总结:我们报告了一位82岁的男性患者,他最初被诊断为前列腺癌,但在前列腺手术和随后的根治性胆囊切除术的磁共振成像中偶然发现GB壁增厚,显示原发性GB MALT淋巴瘤。内科肿瘤学家对患者进行了随访,经过讨论,鉴于无症状表现,决定继续密切监测观察,不进行全身化疗。患者术后16个月无复发。虽然手术前的精确诊断在这个病例中是困难的,术前检查显示一个粘膜下肿瘤样病变。结论:在以往的许多研究中,对GB的MALT淋巴瘤知之甚少。术前诊断真的很难。结合临床表现、术后组织学和免疫组织化学有助于诊断和进行适当的治疗。
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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来源期刊
World Journal of Clinical Cases
World Journal of Clinical Cases Medicine-General Medicine
自引率
0.00%
发文量
3384
期刊介绍: The World Journal of Clinical Cases (WJCC) is a high-quality, peer reviewed, open-access journal. The primary task of WJCC is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of clinical cases. In order to promote productive academic communication, the peer review process for the WJCC is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJCC are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in clinical cases.
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