Acute/subacute ganglionar paracoccidiodomycosis associated with eosinophilia
Abstract
Paracoccidioidomycosis is an endemic mycosis whose initial diagnosis may be difficult, as it shares the clinical characteristics of granulomatous and neoplastic diseases. Although its chronic form is the most frequent, we present the case of a young patient with an acute/subacute presentation with lymphadenopathy, peripheral eosinophilia and a false-positive hepatitis C serology. The diagnosis was confirmed by histopathology and tissue culture, and he was treated with amphotericin B due to clinical deterioration secondary to progression of systemic involvement
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Copyright (c) 2020 Juan Carlos Pineda Ruiz, Angela Patricia Montoya Bernal, Herman Correa López, Xiomara Vanessa Cruz Tangarife, María Cecilia Campiño Martínez
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