Chronic Septic Granulomatosis Revealed in Adulthood by Respiratory Manifestations

Authors

  • Fatima Ezzahra Haouassia Pulmonology Department, Ibn Rochd University Hospital, Casablanca, Morocco
  • Khadija Chaanoun Pulmonology Department, Ibn Rochd University Hospital, Casablanca, Morocco
  • Nahid Zaghba Pulmonology Department, Ibn Rochd University Hospital, Casablanca, Morocco
  • Hanane Benjelloun Pulmonology Department, Ibn Rochd University Hospital, Casablanca, Morocco
  • Najiba Yassine Pulmonology Department, Ibn Rochd University Hospital, Casablanca, Morocco

DOI:

https://doi.org/10.33533/jpm.v18i1.7554

Keywords:

immunodepression, immune disorder, respiratory infections, invasive aspergillosis, chronic septic granulomatosis

Abstract

Chronic septic granulomatosis is a rare genetic disease that affects the immune system. It is characterized by a primary immune deficiency that makes it more difficult for phagocytic cells (such as polymorphonuclear neutrophils, eosinophils, monocytes, and macrophages) to eradicate some harmful bacteria and fungi. It is considered an orphan disease because it affects less than 0.05% of a given population.

References

Salvator, Hélène. "Manifestations pulmonaires chez les adultes atteints de Granulomatose Septique Chronique." DUMAS (Dépôt Universitaire de Mémoires Après Soutenance), 2013. Available from: https://dumas.ccsd.cnrs.fr/dumas-01146108

Salvator, H., Mahlaoui, A., Hurtado-Nedelec, M., Dreyfus, J. F., Durieu, I., Fouyssac, F., Hermine, O., Lortholary, O., Fischer, A., & Couderc, L. J. "Pulmonary Manifestations in Adult Patients with Chronic Granulomatous Disease." 2015. DOI: 10.1183/09031936.00118414

Blumental, S., Mouy, R., Mahlaoui, N.et al (2011). Invasive Mold Infections in Chronic Granulomatous Disease: A 25-Year Retrospective Survey. Clinical Infectious Diseases,53(12),e159–e169. DOI: https://doi.org/10.1093/cid/cir731

Vinuela, Vincent. "Comprehensive Medical Information on Chronic Granulomatous Disease: Study of Complications in Patients Followed at the University Hospital Center of Nancy Over 40 Years." 2018.

Segal BH, DeCarlo ES, Kwon-Chung KJ, Malech HL, Gallin JI, Holland SM. Aspergillus nidulans infection in chronic granulomatous disease. Clin Infect Dis. 1998 Sep;27(3):600-2. DOI: https://doi.org/10.1097/00005792-199809000-00004

Barese, C. N., Goebel, W. S., & Dinauer, M. C. "Gene Therapy for Chronic Granulomatous Disease." 2004. DOI: 10.1517/14712598.4.9.1423

Anderson-Cohen, M., Holland, L., & Roesler, J. "Severe Phenotype of Chronic Granulomatous Disease in a Female with a De Novo Mutation." 2003. DOI: 10.1016/j.clim.2003.08.002

Cale, C. M., Morton, L., & Goldblatt, D. "Cutaneous and Lupus-like Symptoms in Carriers of X-linked Chronic Granulomatous Disease: Incidence and Autoimmune Serology." 2007. DOI: 10.1111/j.1365-2249.2007.03321.x

Cavazzana-Calvo, M., & Fischer, A. "Gene Therapy for Combined Immunodeficiency: Progress and Challenges." DOI: 10.1172/JCI30953

Chatzipanagiotou, S., Takou, K., & Perogamvros, A. "Cutaneous Purulent Aspergillosis in a Young Man with Chronic Granulomatous Disease." 2009. DOI: 10.1111/j.1439-0507.1998.tb00357.x

Holland, Steven M. 2010. DOI: 10.1007/s12016-009-8136-z

Goldblatt, D., & Thrasher, A. J. "Chronic." 2000. DOI: 10.1046/j.1365-2249.2000.01314.x

Jones, L. B. K. R., McGrogan, P., Flood, T. J., Gennery, A. R., Morton, L., Thrasher, A., Goldblatt, D., Parker, L., & Cant, A. J. "Chronic Granulomatous Disease in the United Kingdom." 2008. DOI: 10.1111/j.1365-2249.2008.03644.x

Kuhns, D. B., Gregory Alvord, L., Holland, S. M., & Gallin, J. 2010. DOI: 10.1056/NEJMoa1007097

Liese, J. G., Jendrossek, et al. "Chronic Granulomatous Disease in Adults: Insights from a Study." 1996. DOI: 10.1016/S0140-6736(96)90403-1

Downloads

Published

2024-06-15

How to Cite

Haouassia, F. E., Chaanoun, K., Zaghba, N., Benjelloun, H., & Yassine, N. (2024). Chronic Septic Granulomatosis Revealed in Adulthood by Respiratory Manifestations . Jurnal Profesi Medika : Jurnal Kedokteran Dan Kesehatan, 18(1), 112–118. https://doi.org/10.33533/jpm.v18i1.7554