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Résumé
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.
langue originale | Anglais |
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Pages (de - à) | 787-793 |
Nombre de pages | 7 |
journal | Mycopathologia |
Volume | 184 |
Numéro de publication | 6 |
Les DOIs | |
Etat de la publication | Publié - 1 déc. 2019 |
Modification externe | Oui |
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