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 |
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| container_title | World journal of gastrointestinal pathophysiology |
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| creator | Kotlarz, Daniel Egritas Gurkan, Odul Haskologlu, Zehra Sule Ekinci, Ozgur Aksu Unlusoy, Aysel Gürcan Kaya, Neslihan Puchalka, Jacek Klein, Cristoph Dalgic, Buket |
| description | 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. |
| doi_str_mv | 10.4291/wjgp.v8.i2.87 |
| format | Article |
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| source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
| subjects | Case Report |
| title | Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention |
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