| Literature DB >> 31729682 |
Quentin Binet1, Jacques Mairesse2, Marie Vanthuyne3,4, Jean-Christophe Marot5, Grégoire Wieers5.
Abstract
Pneumocystis pneumonia (PCP) is a life-threatening fungal infection occurring in immunocompromised patients such as HIV-positive patients with low CD4 cell count or patients under heavy immunosuppressive therapy. We report the case of a 59-year-old male with severe diffuse cutaneous systemic sclerosis presenting with asthenia, dry cough and worsening shortness of breath for the last 15 days. Biological studies were remarkable for PTH-independent severe hypercalcemia with low 25-hydroxyvitamin D and a paradoxically elevated 1,25-dihydroxyvitamin D. Early bronchoalveolar lavage allowed for PCP diagnosis and targeted treatment. We discuss the underlying physiopathology and difficulties regarding prophylaxis and treatment.Entities:
Keywords: Hypercalcemia; Immunocompromised; Pneumocystis pneumonia; Systemic sclerosis
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Year: 2019 PMID: 31729682 DOI: 10.1007/s11046-019-00397-w
Source DB: PubMed Journal: Mycopathologia ISSN: 0301-486X Impact factor: 2.574