de Oliveira Santana Marcela A, Butt Saira, Nassiri Mehdi
National Reference Center for Sanitary Dermatology and Leprosy, Federal University of Uberlândia, Uberlândia, BRA.
Infectious Disease, Indiana University School of Medicine, Indianapolis, USA.
Cureus. 2022 Mar 28;14(3):e23572. doi: 10.7759/cureus.23572. eCollection 2022 Mar.
Whipple disease (WD) is a rare systemic infection caused by . Its clinical features are broad, and atypical clinical patterns such as the involvement of the heart, lungs, or the central nervous system (CNS) can occur. We report a case of a 58-year-old man who had been previously diagnosed with classic WD; he was evaluated for functional decline, extreme somnolence, and recurrent admissions for hydrocephalus. The patient was diagnosed with a neurologic relapse of WD after a positive polymerase chain reaction (PCR) from a cerebral spinal fluid (CSF) sample. He was successfully treated with IV ceftriaxone followed by oral trimethoprim-sulfamethoxazole (TMP-SMX). In classic WD, the CNS symptoms usually present in the late phase of the disease or in the form of relapse, especially after an inadequate treatment course. This case highlights the importance of considering CNS involvement in WD when a patient with a previous history of classic WD presents with hypersomnolence, hydrocephalus, or other neurologic symptoms.
惠普尔病(WD)是一种由……引起的罕见的全身性感染。其临床特征广泛,可能出现非典型临床模式,如累及心脏、肺部或中枢神经系统(CNS)。我们报告一例58岁男性病例,该患者此前被诊断为经典型WD;他因功能衰退、极度嗜睡以及因脑积水反复入院而接受评估。在脑脊液(CSF)样本聚合酶链反应(PCR)呈阳性后,该患者被诊断为WD的神经系统复发。他先接受静脉注射头孢曲松治疗,随后口服甲氧苄啶-磺胺甲恶唑(TMP-SMX),治疗成功。在经典型WD中,CNS症状通常出现在疾病晚期或以复发形式出现,尤其是在治疗疗程不足之后。该病例强调,当有经典型WD病史的患者出现嗜睡、脑积水或其他神经系统症状时,考虑WD累及CNS的重要性。