Portela Romero M, Ventura Victoria M A, Iglesias Otero M, do Muiño Joga M, Bugarín González R
Medicina de Familia y Comunitaria, Centro de Salud de Padrón, Gerencia de Gestión Integrada de Santiago de Compostela, Servicio Gallego de Salud, Santiago de Compostela, España.
Semergen. 2013 Nov-Dec;39(8):450-2. doi: 10.1016/j.semerg.2012.07.008. Epub 2012 Sep 13.
Granulomatous cheilitis is a rare disease included among the orofacial granulomatoses. It is characterized by a idiopathic chronic inflammation of the labial mucosa (macrochelia), which takes the form of episodic and progressive outbreaks. In 10% of patients, it is associated with Crohn's disease. We report the presentation, evaluation and treatment of a case of granulomatous cheilitis which appearted two years after the onset of Crohn's disease. We conclude that granulomatous cheilitis is rare in children, with few reported cases, although probably underdiagnosed because of lack of awareness. The diagnosis of granulomatous cheilitis is clinical, although the histological evaluation is a determining factor. After making the diagnosis a comprehensive assessment of the patient is recommended, to rule out the other associated syndromes described in the literature.
肉芽肿性唇炎是一种罕见疾病,属于口面部肉芽肿病。其特征为唇黏膜特发性慢性炎症(巨唇),呈发作性和进行性发作。10%的患者与克罗恩病相关。我们报告了1例在克罗恩病发病两年后出现的肉芽肿性唇炎病例的临床表现、评估及治疗。我们得出结论,肉芽肿性唇炎在儿童中罕见,报道病例较少,尽管可能因认识不足而诊断不足。肉芽肿性唇炎的诊断主要依靠临床,但组织学评估是一个决定性因素。确诊后建议对患者进行全面评估,以排除文献中描述的其他相关综合征。