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重度难治性口腔面部克罗恩病:一例报告

Severe refractory orofacial Crohn's disease: report of a case.

作者信息

Quezada Sandra, Turner Patricia L, Alexiev Borislav, Daly Barry, Cross Raymond

机构信息

Department of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

出版信息

Dig Dis Sci. 2009 Oct;54(10):2290-5. doi: 10.1007/s10620-008-0588-0. Epub 2008 Dec 10.

DOI:10.1007/s10620-008-0588-0
PMID:19082722
Abstract

Oral involvement is common in patients with Crohn's disease (CD) and can precede intestinal symptoms, making diagnosis difficult. We report a case of severe orofacial CD. A 41-year-old woman presented with palate and tongue ulcers. Biopsies showed acute inflammation with ulcer. Colonoscopy demonstrated ascending colon ulceration. Biopsies revealed acute colitis and mild architectural distortion. Prednisone was started but the symptoms recurred with taper; steroids were resumed and infliximab (IFX) 5 mg/kg was infused. After improvement, oral pain and weight loss returned. A G tube was placed. Mercaptopurine was started at 1.5 mg/kg per day. IFX was increased to 10 mg/kg. Debridement of the oral ulcers and a skin graft to the lips was performed. Pathology from oral and facial lesions was consistent with granulation tissue and fibrosis with chronic inflammation. She was readmitted several months later for weight loss and dehydration. Abdominal pain, distension, and feculent drainage developed around the G tube. Repeat computed tomography (CT) scan demonstrated pneumatosis. Laparotomy revealed purulent drainage from a perforated segment of sigmoid colon. Histology was consistent with perforated CD. Despite ventilatory and hemodynamic support and broad-spectrum antibiotics, the patient died 1 week later. Our case highlights the difficulty in diagnosing and managing orofacial CD. In this case, medical treatment was initiated based on a high index of suspicion. CD was only confirmed after intestinal resection very late in the disease course. Treatment of orofacial CD includes topical or systemic steroids, immunomodulators, and anti-tumor necrosis factor (TNF) therapies. As our case demonstrated, patients can be refractory to therapy.

摘要

口腔受累在克罗恩病(CD)患者中很常见,且可能先于肠道症状出现,这使得诊断变得困难。我们报告一例严重的口面部克罗恩病病例。一名41岁女性出现腭部和舌部溃疡。活检显示溃疡处有急性炎症。结肠镜检查显示升结肠溃疡。活检显示急性结肠炎和轻度结构扭曲。开始使用泼尼松,但症状在减量时复发;恢复使用类固醇,并输注英夫利昔单抗(IFX)5mg/kg。病情改善后,口腔疼痛和体重减轻又复发。放置了胃造瘘管。开始每天使用1.5mg/kg的巯嘌呤。IFX增加至10mg/kg。对口部溃疡进行清创,并对唇部进行植皮。口腔和面部病变的病理检查结果与伴有慢性炎症的肉芽组织和纤维化一致。几个月后,她因体重减轻和脱水再次入院。胃造瘘管周围出现腹痛、腹胀和粪便样引流物。重复计算机断层扫描(CT)显示有积气。剖腹探查发现乙状结肠穿孔段有脓性引流物。组织学检查结果与穿孔性克罗恩病一致。尽管给予了通气和血流动力学支持以及广谱抗生素治疗,患者1周后仍死亡。我们的病例突出了口面部克罗恩病诊断和管理的困难。在该病例中,基于高度怀疑开始了药物治疗。直到疾病病程很晚进行肠道切除后才确诊为克罗恩病。口面部克罗恩病的治疗包括局部或全身使用类固醇、免疫调节剂和抗肿瘤坏死因子(TNF)疗法。正如我们的病例所示,患者可能对治疗无效。

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本文引用的文献

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