Kotlarz Daniel, Egritas Gurkan Odul, Haskologlu Zehra Sule, Ekinci Ozgur, Aksu Unlusoy Aysel, Gürcan Kaya Neslihan, Puchalka Jacek, Klein Cristoph, Dalgic Buket
Daniel Kotlarz, Jacek Puchalka, Cristoph Klein, Department of Pediatrics Dr. Von Hauner Children's Hospital, Ludwig-Maximilians-University, 80539 Munich, Germany.
World J Gastrointest Pathophysiol. 2017 May 15;8(2):87-92. doi: 10.4291/wjgp.v8.i2.87.
Chronic granulomatous disease (CGD) is a primary immune deficiency that is commonly diagnosed under the age of 5 years (95%) and is rarely seen in adulthood. CGD may manifest as inflammatory bowel disease (IBD) in childhood. Without proper diagnosis, these patients may be monitored for years as IBD; some may even be regarded as steroid-resistant ulcerative colitis (UC) and end up having a colectomy. In this case report, we described a patient who had been followed-up for years as UC and subsequently underwent colectomy, but was finally diagnosed in adulthood as primary immune deficiency.