A Rare Case of Primary B-Cell Lymphoma of the Pancreas.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of investigative medicine high impact case reports Pub Date : 2024-01-01 DOI:10.1177/23247096241263536
Dayana Nasr, John Joyce, Vishnu Kumar, Hafiz M Khan, Savio John, Sidhartha Chaudhry
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引用次数: 0

Abstract

Primary pancreatic lymphomas (PPLs) are a subgroup of gastrointestinal (GI) lymphomas. They are an exceedingly rare entity, both in terms of pancreatic malignancies and also extranodal lymphomas. Epidemiological investigations have been challenging to do because of their rarity. This has resulted in a lack of clarity on the clinicopathological characteristics, differential diagnosis, best course of treatment, and prognosis of PPL. Because the clinical signs are frequently non-specific, it can lead to a diagnostic hazard for the unwary physician. Preoperatively, it is imperative to distinguish between adenocarcinoma and PPL, as they present similarly, but have vastly different treatment modalities and prognosis. We herein present a case of an elderly man who presented with obstructive jaundice and was found to have PPL.

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一个罕见的胰腺原发性 B 细胞淋巴瘤病例
原发性胰腺淋巴瘤(PPL)是胃肠道淋巴瘤的一个亚组。无论是在胰腺恶性肿瘤还是结节外淋巴瘤中,它们都极为罕见。由于其罕见性,流行病学调查一直是一项挑战。这导致 PPL 的临床病理特征、鉴别诊断、最佳治疗方案和预后都不明确。由于临床表现往往没有特异性,这可能会给缺乏警惕性的医生带来诊断上的隐患。术前必须区分腺癌和 PPL,因为它们表现相似,但治疗方式和预后却大相径庭。我们在此介绍一例因阻塞性黄疸就诊的老年男性,他被发现患有 PPL。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
165
审稿时长
12 weeks
期刊介绍: The AFMR is committed to enhancing the training and career development of our members and to furthering its mission to facilitate the conduct of research to improve medical care. Case reports represent an important avenue for trainees (interns, residents, and fellows) and early-stage faculty to demonstrate productive, scholarly activity.
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