Hypercalcemia Heralding Pneumocystis jirovecii Pneumonia in an HIV-Seronegative Patient with Diffuse Cutaneous Systemic Sclerosis.

Binet, Quentin;Mairesse, Jacques;Vanthuyne, Marie;Marot, Jean-Christophe;Wieers, Grégoire
(2019) Mycopathologia — Vol. 184, n° 6, p. 787-793 (2019)

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  • Binet, Quentinorcid-logo
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  • Mairesse, Jacques
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  • Marot, Jean-Christophe
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  • Wieers, Grégoire
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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.
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Binet, Q., Mairesse, J., Vanthuyne, M., Marot, J.-C., & Wieers, G. (2019). Hypercalcemia Heralding Pneumocystis jirovecii Pneumonia in an HIV-Seronegative Patient with Diffuse Cutaneous Systemic Sclerosis. Mycopathologia, 184(6), 787-793. https://doi.org/10.1007/s11046-019-00397-w (Original work published 2019)