disseminated penicilliosis due to penicillium chrysogenum in a pediatric patient with henoch–schönlein syndrome

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ID: 249875
2016
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Abstract
A case of disseminated infection caused by Penicillium chrysogenum in a 10-year-old boy with a history of Henoch–Schönlein purpura and proliferative glomerulonephritis, treated with immunosuppressors, is reported herein. The patient had a clinical picture of 2 weeks of fever that did not respond to treatment with broad-spectrum antibiotics and amphotericin B. Computed tomography imaging showed diffuse cotton-like infiltrates in the lungs, hepatomegaly, mesenteric lymphadenopathy, and multiple well-defined round hypodense lesions in the spleen. His treatment was changed to caspofungin, followed by voriconazole. One month later, a splenic biopsy revealed hyaline septate hyphae of > 1 μm in diameter. Fungal growth was negative. However, molecular analysis showed 99% identity with P. chrysogenum. A therapeutic splenectomy was performed, and treatment was changed to amphotericin B lipid complex and caspofungin. The patient completed 2 months of treatment with resolution of the infection. P. chrysogenum is a rare causative agent of invasive fungal infections in immunocompromised patients, and its diagnosis is necessary to initiate the appropriate antifungal treatment.
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avils-robles2016internationaldisseminated Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Martha Avilés-Robles;Carlos Gómez-Ponce;Jesús Reséndiz-Sánchez;Aída Verónica Rodríguez-Tovar;Adrián Ceballos-Bocanegra;Ángeles Martínez-Rivera
Journal israel journal of chemistry
Year 2016
DOI
10.1016/j.ijid.2016.08.026
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