FAMILIAL CHRONIC GRANULOMATOUS DISEASE

Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder of phagocytes, characterized by repeated bacterial and fungal infections. We present a boy suffering from recurrent infections since infancy who was treated with various antibiotics and anti-tuberculosis medicines withou...

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Autores principales: Tariq Ghafoor, Farrah Bashir
Formato: article
Lenguaje:EN
Publicado: Army Medical College Rawalpindi 2019
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Acceso en línea:https://doaj.org/article/771d19490f8a4404a6bae68bf96828c0
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spelling oai:doaj.org-article:771d19490f8a4404a6bae68bf96828c02021-11-16T05:28:48ZFAMILIAL CHRONIC GRANULOMATOUS DISEASE0030-96482411-8842https://doaj.org/article/771d19490f8a4404a6bae68bf96828c02019-02-01T00:00:00Zhttps://www.pafmj.org/index.php/PAFMJ/article/view/2525/2080https://doaj.org/toc/0030-9648https://doaj.org/toc/2411-8842Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder of phagocytes, characterized by repeated bacterial and fungal infections. We present a boy suffering from recurrent infections since infancy who was treated with various antibiotics and anti-tuberculosis medicines without any relief. All four of his brothers had recurrent respiratory tract infections and were treated empirically with anti-tuberculosis; all of them expired one after the other without any definitive diagnosis. He was diagnosed at ten years of age with pulmonary aspergillosis and CGD. This case highlights pitfalls of medical management of chronic cases in our society. Because of TB endemic area, it is a common practice among physicians to start anti-tuberculosis medicines without making a definite diagnosis. We recommend thorough investigations including testing for CGD in every patient with recurrent or persistent infections especially if other siblings also have similar manifestations.Tariq GhafoorFarrah BashirArmy Medical College Rawalpindiarticletuberculosischronic granulomatous diseaseMedicineRMedicine (General)R5-920ENPakistan Armed Forces Medical Journal, Vol 69, Iss 1, Pp 217-220 (2019)
institution DOAJ
collection DOAJ
language EN
topic tuberculosis
chronic granulomatous disease
Medicine
R
Medicine (General)
R5-920
spellingShingle tuberculosis
chronic granulomatous disease
Medicine
R
Medicine (General)
R5-920
Tariq Ghafoor
Farrah Bashir
FAMILIAL CHRONIC GRANULOMATOUS DISEASE
description Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder of phagocytes, characterized by repeated bacterial and fungal infections. We present a boy suffering from recurrent infections since infancy who was treated with various antibiotics and anti-tuberculosis medicines without any relief. All four of his brothers had recurrent respiratory tract infections and were treated empirically with anti-tuberculosis; all of them expired one after the other without any definitive diagnosis. He was diagnosed at ten years of age with pulmonary aspergillosis and CGD. This case highlights pitfalls of medical management of chronic cases in our society. Because of TB endemic area, it is a common practice among physicians to start anti-tuberculosis medicines without making a definite diagnosis. We recommend thorough investigations including testing for CGD in every patient with recurrent or persistent infections especially if other siblings also have similar manifestations.
format article
author Tariq Ghafoor
Farrah Bashir
author_facet Tariq Ghafoor
Farrah Bashir
author_sort Tariq Ghafoor
title FAMILIAL CHRONIC GRANULOMATOUS DISEASE
title_short FAMILIAL CHRONIC GRANULOMATOUS DISEASE
title_full FAMILIAL CHRONIC GRANULOMATOUS DISEASE
title_fullStr FAMILIAL CHRONIC GRANULOMATOUS DISEASE
title_full_unstemmed FAMILIAL CHRONIC GRANULOMATOUS DISEASE
title_sort familial chronic granulomatous disease
publisher Army Medical College Rawalpindi
publishDate 2019
url https://doaj.org/article/771d19490f8a4404a6bae68bf96828c0
work_keys_str_mv AT tariqghafoor familialchronicgranulomatousdisease
AT farrahbashir familialchronicgranulomatousdisease
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