Journals / Turkish Thoracic Journal / 2016 / Cilt: 17 - Sayı: 4

Two Chronic Granulomatous Disease Diagnosed in Adult Age

Pages
163–167
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

These two cases signify that, in our country where consanguinity is common, etiology of recurrent unexplained infections, abscesses and granulomas should be investigated and CGD should be in differantial diagnosis list.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Chronic granulomatous disease (CGD) is a rare, inherited primary immunodeficiency that is usually diagnosed at adulthood and is presented with recurrent bacterial and fungal infections.
📊
Key Findings & Data:A 29-yearold woman was referred to our clinic with hypoxic respiratory failure, with a pre-diagnosis of multidrug resistant tuberculosis (TB).
💡
Conclusion & Impact:These two cases signify that, in our country where consanguinity is common, etiology of recurrent unexplained infections, abscesses and granulomas should be investigated and CGD should be in differantial diagnosis list.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Chronic granulomatous disease (CGD) is a rare, inherited primary immunodeficiency that is usually diagnosed at adulthood and is presented with recurrent bacterial and fungal infections. In this case report, two adult cases of CGD have been presented. A 29-yearold woman was referred to our clinic with hypoxic respiratory failure, with a pre-diagnosis of multidrug resistant tuberculosis (TB). Her lung biopsy had been reported as granulomatous inflammation, she hadnot responded to a 5 month anti-TB treatment. A complete medical history consisted of 4 occasions of treatment with anti-TB drugs and that her sister and brother had undergone TB therapy. However, since childhood, a TB bacilli had never been isolated microbiologically in the siblings. Patient's parents were third degree consanguineous. The patient still had a purulent drainage around the operation site. Microbiological studies of the wound drainage and respiratory tract have not encountered any specific microorganism. Investigation of an immunodeficiency has proved CGD through nitroblue tetrazolium test. Her siblings has been diagnosed as CGD as well. Second case, a 19-year-old male, has been admitted to our clinic with complaints of fever, chest pain and an abscess lesion in the anterior chest wall. His medical history comprised 3 recurrences of pneumonia within last 2 years. In physical examination, a 3 x 5 cm fluctuant swelling lesion on the anterior chest wall. Radiologically, new pneumonic consolidations were detected. Sputum specimens did not provide any specific microorganism, cultures of the chest-wall abscess fluid grew aspergillus. His parents had been living in the same village but no consanguinity was known. Due to recurrent infections, immunodeficiency tests had been investigated. He was diagnosed as CGD due to dihydrorhodamin test. These two cases signify that, in our country where consanguinity is common, etiology of recurrent unexplained infections, abscesses and granulomas should be investigated and CGD should be in differantial diagnosis list.

🔖

Cite This Article

AKYIL, F. T., SEVİM, T., BARIŞ, S., AKSOY, E., TOKYAY, D. A., BODUR, Y., AKTAŞ, O. (2016). Two Chronic Granulomatous Disease Diagnosed in Adult Age. Turkish Thoracic Journal, Cilt: 17 - Sayı: 4, 163–167. https://ajindex.com/articles/418081

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. Holland SM. Chronic granulomatous disease. Clin Rev Allergy Immunol 2010;38:3-10. [CrossRef] 2. Song E, Jaishankar GB, Saleh H, et al. Chronic granulomatous disease: a review of the infectious and inflammatory complications. Clin Mol Allergy 2011;9:10. [CrossRef] 3. Stasia MJ, Li XJ. Genetics and immunopathology of chronic granulomatous disease. Semin Immunopathol 2008;30:209-35. [CrossRef] 4. Winkelstein JA, Marino MC, Johnston RB Jr, et al. Chronic granulomatous disease. Report on a national registry of 368 patients. Medicine (Baltimore) 2000;79:155-69. [CrossRef] 5. Filiz S, Kocacık Uygun DF, Yeğin O. Kronik granülomatöz hastalık. Turk J Immunol 2013;1:22-31. [CrossRef] 6. Ramanuja S, Wolf KM, Sadat MA, et al. Newly diagnosed chronic granulomatous disease in a 53-year-old woman with Crohn disease. Ann Allergy Asthma Immunol 2005;95:204-9. [CrossRef] 7. Chung AG, Cyr MM, Ellis AK. Newly diagnosed chronic granulomatous disease in a 44 year old male presenting with recurrent groin cellulitis and colitis. Allergy Asthma Clin Immunol 2013;9:9. [CrossRef] 8. Dorman SE, Guide SV, Conville PS, et al. Nocardia infection in chronic granulomatous disease. Clin Infect Dis 2002;35:390-4. [CrossRef] 9. Segal BH, DeCarlo ES, Kwon-Chung KJ, et al. Aspergillus nidulans infection in chronic granulomatous disease. Medicine (Baltimore) 1998;77:345-54. [CrossRef] 10. Buescher ES, Gallin JI. Stature and weight in chronic granulomatous disease. J Pediatr 1984;104:911-3. [CrossRef] 11. Wintergest U, Rosenzweig SD, Abinon M, et al. Phagocyte defects. In: Rezai N, Aghamohammadi A, Notarangelo LD (eds). Primary immundeficiency diseases: definition diagnosis and treatment. Berlin: Springer Verlag, 2008:143-52. 12. Marciano BE, Rosenzweig SD, Kleiner DE, et al. Gastrointestinal involvement in chronic granulomatous disease. Pediatrics 2004;114:462-8. [CrossRef] 13. Roos D, Kuijpers TW, Curnette JT. Chronic granulamatous disease. In: Ochs HD, Smith CIE, Puck JM (eds). Primary immunodefiency diseases. A molecular and genetic approach. 2th ed. New York: Oxford University Press, 2007:527-49. 14. Bustamante J, Aksu G, Vogt G. BCG-osis and tuberculosis in a child with chronic granulomatous disease. J Allergy Clin Immunol 2007;120:32-38. [CrossRef] 15. Segal BH, Leto TL, Gallin JI, et al. Genetic, biochemical, and clinical features of chronic granulomatous disease. Medicine (Baltimore) 2000;79:170-200. [CrossRef]