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一例罕见的腹膜后原发性滤泡性淋巴瘤

A Rare Case of Primary Follicular Lymphoma in the Retroperitoneum.

作者信息

Mathew Tijin, Hariprasad Shree, Varghese Teresa, George Lydia, Easow Benjamin, Adrejiya Parth, Gevorgian Melinda, Thomas Greeshma, Zafar Tehmina

机构信息

Internal Medicine, Southeast Health Medical Center, Dothan, USA.

Internal Medicine, Alabama College of Osteopathic Medicine, Dothan, USA.

出版信息

Cureus. 2025 Mar 27;17(3):e81288. doi: 10.7759/cureus.81288. eCollection 2025 Mar.

Abstract

Primary retroperitoneal non-Hodgkin lymphoma (NHL) is considered sporadic, difficult to diagnose, and has an atypical presentation. NHL typically presents with non-tender peripheral lymphadenopathy in two-thirds of patients. Very rarely, it may present with abdominal swelling and obstructive symptoms of the respiratory and GI tracts. The primary gastrointestinal NHL accounts for 5-20% of all extra-nodal lymphomas. However, there are only a few reported cases of primary retroperitoneal lymphomas. Among them, most were diffuse large B cell lymphomas. This case is of a 54-year-old male patient who presented to the emergency department with abdominal swelling for the past four months. The CT abdomen and pelvis were indicative of massive retroperitoneal and mesenteric adenopathy with concerns for lymphoma with some volume ascites. He underwent an interventional radiology (IR)-guided retroperitoneal lymph node biopsy. Given his pleural effusion on the CT abdomen and pelvis, a CT chest was ordered, which showed loculated left-sided pleural effusion and trace pleural effusion on the right side. His lymph node biopsy results revealed grade II follicular lymphoma. This case highlights the atypical presentation of follicular lymphoma and that it should be considered in the differential diagnosis when a patient presents with pleural effusion or ascites, even though there are no B symptoms. Because of its indolence, follicular lymphoma is often diagnosed when a patient presents with obstructive symptoms and other complications like peritoneal carcinomatosis. Early diagnosis and treatment can lead to good clinical outcomes.

摘要

原发性腹膜后非霍奇金淋巴瘤(NHL)被认为是散发性的,诊断困难,且表现不典型。三分之二的NHL患者通常表现为无痛性外周淋巴结病。极少数情况下,它可能表现为腹部肿胀以及呼吸道和胃肠道的梗阻症状。原发性胃肠道NHL占所有结外淋巴瘤的5% - 20%。然而,原发性腹膜后淋巴瘤的报道病例很少。其中,大多数是弥漫性大B细胞淋巴瘤。该病例为一名54岁男性患者,因过去四个月来腹部肿胀到急诊科就诊。腹部和盆腔CT显示大量腹膜后和肠系膜淋巴结肿大,怀疑为淋巴瘤,并伴有少量腹水。他接受了介入放射学(IR)引导下的腹膜后淋巴结活检。鉴于其腹部和盆腔CT显示有胸腔积液,遂进行胸部CT检查,结果显示左侧胸腔有局限性胸腔积液,右侧有微量胸腔积液。他的淋巴结活检结果显示为II级滤泡性淋巴瘤。该病例突出了滤泡性淋巴瘤的非典型表现,即当患者出现胸腔积液或腹水时,即使没有B症状,在鉴别诊断中也应考虑到该病。由于其惰性,滤泡性淋巴瘤常在患者出现梗阻症状和其他并发症如腹膜癌病时才被诊断出来。早期诊断和治疗可带来良好的临床结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d70c/12033966/614b8d028f93/cureus-0017-00000081288-i01.jpg

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