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Disseminated histoplasmosis: a rare clinical phenotype with difficult diagnosis

We describe a rare and interesting case of a 37‐year‐old man who presented with an intermittent fever, progressive cytopenia, and hepatosplenomegaly. Histopathological examination of a bone marrow smear revealed haemophagocytes and intracellular yeast‐like Histoplasma capsulatum (H. capsulatum); thu...

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Detalles Bibliográficos
Autores principales: Xiong, Xiao‐feng, Fan, Li‐li, Kang, Mei, Wei, Jia, Cheng, De‐yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326786/
https://www.ncbi.nlm.nih.gov/pubmed/28250930
http://dx.doi.org/10.1002/rcr2.220
Descripción
Sumario:We describe a rare and interesting case of a 37‐year‐old man who presented with an intermittent fever, progressive cytopenia, and hepatosplenomegaly. Histopathological examination of a bone marrow smear revealed haemophagocytes and intracellular yeast‐like Histoplasma capsulatum (H. capsulatum); thus, we prolonged the blood culture duration to detect fungi, and H. capsulatum was detected in the peripheral blood. After the diagnosis of disseminated histoplasmosis, the patient was successfully treated with amphotericin B and symptomatic therapy. This is the first case in southwest China for which H. capsulatum was cultivated in peripheral blood, illustrating that the duration of specimen culture should be lengthened if a specific pathogen infection is suspected. Moreover, this case enriches our understanding of clinical manifestations of disseminated histoplasmosis.