| Literature DB >> 26192294 |
Toshiko Onitake1, Yoshitaka Ueno2, Shinji Tanaka2, Rie Hanaoka3, Kyoko Yoshioka3, Tsuyoshi Hatakeyama3, Shiro Oka2, Shigeto Yoshida2, Toru Hiyama4, Masanori Ito3, Yasuhiko Kitadai3, Masaharu Yoshihara4, Kazuaki Chayama3.
Abstract
Cheilitis granulomatosa (CG) is a rare disease, which presents usually as a persistent swelling of the soft tissues in the orofacial region and is characterized histologically by a granulomatous inflammation. We report the case of a 19-year-old man who suffered from anal fistula. The patient had a 6-year history of asymptomatic and persistent swelling of the lower lip. Examinations for gastrointestinal lesions containing double-balloon total enteroscopy revealed erosions located longitudinally throughout the small intestine and the patient was diagnosed Crohn's disease (CD). Biopsy of the lower lip showed non-caseating granuloma and confirmed the diagnosis of CG. Despite an elemental diet and mesalazine therapy, the lip swelling persisted. The CG can be the first presenting symptom of CD. CG as a complication of CD is discussed.Entities:
Keywords: Crohn’s disease; Orofacial granulomatosis
Year: 2009 PMID: 26192294 DOI: 10.1007/s12328-009-0084-x
Source DB: PubMed Journal: Clin J Gastroenterol ISSN: 1865-7265