We report the first description of visceral leishmaniasis (VL) infection as a harbinger of chronic granulomatous disease (CGD) in a 3-year old child. Although VL is not frequently suspected in CGD patients, our case emphasises the importance of a complete evaluation of the immune system in children presenting with VL in order to exclude underlying immunodeficiency states. As the prognosis of CGD is poor, with high morbidity and mortality, establishing an early diagnosis has important practical implications in the successful treatment of these patients. Following the diagnosis, the patient received Human Leukocyte Antigen (HLA) identical sibling bone marrow transplantation (BMT). The child is now 2 years post-transplant and is in good general conditions with normal blood counts, and evidence of full-donor chimerism in repeated fluorescence in situ hybridization (FISH) studies

Finocchi, A., Palma, P., DI MATTEO, G., Chiriaco, M., Lancella, L., Simonetti, A., et al. (2008). Visceral leishmaniasis revealing chronic granulomatous diseases in a child. INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 21(3), 739-743.

Visceral leishmaniasis revealing chronic granulomatous diseases in a child

FINOCCHI, ANDREA;Palma, P;DI MATTEO, GIGLIOLA;SIMONETTI, ALESSANDRA;ROSSI, PAOLO
2008-07-01

Abstract

We report the first description of visceral leishmaniasis (VL) infection as a harbinger of chronic granulomatous disease (CGD) in a 3-year old child. Although VL is not frequently suspected in CGD patients, our case emphasises the importance of a complete evaluation of the immune system in children presenting with VL in order to exclude underlying immunodeficiency states. As the prognosis of CGD is poor, with high morbidity and mortality, establishing an early diagnosis has important practical implications in the successful treatment of these patients. Following the diagnosis, the patient received Human Leukocyte Antigen (HLA) identical sibling bone marrow transplantation (BMT). The child is now 2 years post-transplant and is in good general conditions with normal blood counts, and evidence of full-donor chimerism in repeated fluorescence in situ hybridization (FISH) studies
1-lug-2008
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA
English
Con Impact Factor ISI
Bone marrow transplant; Children; Chronic granulomatous disease; Immunodeficiency; Visceral leishmaniasis
Finocchi, A., Palma, P., DI MATTEO, G., Chiriaco, M., Lancella, L., Simonetti, A., et al. (2008). Visceral leishmaniasis revealing chronic granulomatous diseases in a child. INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 21(3), 739-743.
Finocchi, A; Palma, P; DI MATTEO, G; Chiriaco, M; Lancella, L; Simonetti, A; Rana, I; Livadiotti, S; Rossi, P
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/30514
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