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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Army Medical College Rawalpindi
2019
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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 |
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collection |
DOAJ |
language |
EN |
topic |
tuberculosis chronic granulomatous disease Medicine R Medicine (General) R5-920 |
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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 |
_version_ |
1718426673435639808 |