Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention

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; so...

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Veröffentlicht in:World journal of gastrointestinal pathophysiology 2017-05, Vol.8 (2), p.87-92
Hauptverfasser: Kotlarz, Daniel, Egritas Gurkan, Odul, Haskologlu, Zehra Sule, Ekinci, Ozgur, Aksu Unlusoy, Aysel, Gürcan Kaya, Neslihan, Puchalka, Jacek, Klein, Cristoph, Dalgic, Buket
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Sprache:eng
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Zusammenfassung: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 followedup for years as UC and subsequently underwent colectomy, but was finally diagnosed in adulthood as primary immune deficiency.
ISSN:2150-5330
2150-5330
DOI:10.4291/wjgp.v8.i2.87