| Literature DB >> 28758089 |
Dayun Park1, Ho Jun Lee1, Kwang Hoon Lee2, Bum Sun Kwon1, Jin-Woo Park1, Ki Yeun Nam1, Kyoung Hwan Lee1.
Abstract
Churg-Strauss syndrome (CSS) is a rare systemic vasculitis that affect small and medium-sized blood vessels and is accompanied by asthma, eosinophilia, and peripheral neuropathy. This report describes a case of a 52-year-old man who had a history of sinusitis, asthma, and thymus cancer and who had complained of bilateral lower extremity paresthesia and weakness for a month. Peripheral neuropathy was detected by electrodiagnostic studies. Resection of a mediastinal mass, which was diagnosed as thymic neuroendocrine carcinoma, was performed five months before his visit. After thymectomy, peripheral blood tests revealed a gradual increase in eosinophils. Two months after surgery, he was admitted to the hospital for dyspnea, and nodules of focal consolidation were found in his chest X-ray. One month later, pyoderma occurred in the right shin, and the skin biopsy showed extravascular eosinophilic infiltration. He was diagnosed with CSS after thymectomy, and we report a very rare case of CSS presented with thymic neuroendocrine carcinoma.Entities:
Keywords: Churg-Strauss syndrome; Polyneuropathy; Thymic neuroendocrine carcinoma
Year: 2017 PMID: 28758089 PMCID: PMC5532357 DOI: 10.5535/arm.2017.41.3.493
Source DB: PubMed Journal: Ann Rehabil Med ISSN: 2234-0645