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Disseminated histoplasmosis in primary Sjögren syndrome: A case report
Author(s) -
Jiaai Li,
Yingying Cheng,
Zhi-Tao Cui,
Wei Jiang,
Wuqiong Zhang,
Zhonghua Du,
Bin Gao,
Yinyin Xie,
Hongmei Meng
Publication year - 2020
Publication title -
world journal of clinical cases
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.368
H-Index - 10
ISSN - 2307-8960
DOI - 10.12998/wjcc.v8.i7.1319
Subject(s) - medicine , pancytopenia , histoplasmosis , dimorphic fungus , dermatology , somnolence , rare disease , lymphocytic infiltration , dysphagia , pathology , disease , bone marrow , surgery , adverse effect , genetics , biology , yeast
Sjögren syndrome (SS) is a chronic and systemic autoimmune disease characterized by lymphocytic infiltration of the exocrine glands. And histoplasmosis is an invasive mycosis caused by the saprophytic dimorphic fungus H. capsulatum . In patients with primary SS (PSS), disseminated histoplasmosis (DH) is extremely rare.

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