A Rare Manifestation of a Rare Disease: Nodular Lymphocyte-Predominant Hodgkin Lymphoma Presenting As Paraneoplastic Aseptic Meningitis.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2025-06-18 eCollection Date: 2025-06-01 DOI:10.7759/cureus.86327
Aishwarya Saripalli, Elaine Deemer, Kasey Fox
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Abstract

Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is an uncommon form of Hodgkin lymphoma (HL). It commonly presents as chronic, asymptomatic, slow-growing peripheral lymphadenopathy. Central nervous system involvement in NLPHL is rare. Here we report a case of a 28-year-old male patient who presented with a seven-week history of headache and neck pain. The evaluation revealed a diagnosis of subacute meningitis. He was newly diagnosed with NLPHL on lymph node biopsy. With this presentation of subacute aseptic meningitis with a negative workup for infectious, autoimmune etiology, and absence of malignant cells in the CSF, in the setting of newly diagnosed NLPHL, a diagnosis of paraneoplastic aseptic meningitis was made. The patient improved symptomatically with the treatment of his cancer.

一罕见疾病的罕见表现:结节性淋巴细胞为主的霍奇金淋巴瘤表现为副肿瘤性无菌性脑膜炎。
结节性淋巴细胞显性霍奇金淋巴瘤(NLPHL)是一种罕见的霍奇金淋巴瘤(HL)。它通常表现为慢性、无症状、生长缓慢的周围淋巴结病。中枢神经系统受累在NLPHL是罕见的。在这里我们报告一个28岁的男性病人谁提出了七周的头痛和颈部疼痛的历史。检查显示诊断为亚急性脑膜炎。他在淋巴结活检中被诊断为NLPHL。随着亚急性无菌性脑膜炎的出现,感染性、自身免疫性病因检查阴性,脑脊液中没有恶性细胞,在新诊断的NLPHL的背景下,诊断为副肿瘤性无菌性脑膜炎。病人接受癌症治疗后,症状有所好转。
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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