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外阴克罗恩病的临床经验与诊断算法

Clinical experience and diagnostic algorithm of vulval Crohn's disease.

作者信息

Boxhoorn Lotte, Stoof Tom J, de Meij Tim, Hoentjen Frank, Oldenburg Bas, Bouma Gerd, Löwenberg Mark, van Bodegraven Adriaan A, de Boer Nanne K H

机构信息

Departments of aGastroenterology and Hepatology bGynaecology cPediatric Gastroenterology, VU University Medical Center dDepartment of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam eDepartment of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen fDepartment of Gastroenterology and Hepatology, University Medical Center, Utrecht gDepartment of Gastroenterology, Geriatrics, Internal and Intensive Care Medicine, Zuyderland Medical Center, Heerlen-Sittard-Geleen, The Netherlands.

出版信息

Eur J Gastroenterol Hepatol. 2017 Jul;29(7):838-843. doi: 10.1097/MEG.0000000000000879.

Abstract

BACKGROUND AND AIM

Vulval Crohn's disease (VCD) is a rare extraintestinal cutaneous manifestation of Crohn's disease. No consensus on the diagnostic workup and therapeutic management of this condition has been provided in the current literature.

PATIENTS AND METHODS

Retrospective, multicentre descriptive case series of female patients diagnosed and treated with VCD. By chart review, data on initial symptoms, clinical courses, histologic findings and therapeutic management were collected.

RESULTS

Fifteen female patients with a median age of 28 years (interquartile range: 28-44 years) suffering from Crohn's disease of the ileum (27%), colon (33%) and ileocolon (40%) were included. VCD manifested most frequently with vulval swelling (93%), pain (80%) and erythema (73%). Histologic analysis demonstrated granulomatous inflammation in 78% and a mixed inflammatory cell infiltrate in 67% of cases. In eight (53%) cases, topical therapy resulted in temporary reduction of vulval symptoms. Combotreatment with immunosuppressive agents and tumour necrosis factor α inhibitors was the most effective second-line therapy: five (33%) patients achieved sustained clinical remission with this therapeutic strategy.

CONCLUSION

The diagnostic workup of VCD is challenging and should be approached in a multidisciplinary manner. Histopathologic analysis of the vulva supports the diagnosis. Topical therapy and systemic treatment with immunosuppressive agents and tumour necrosis factor α inhibitors are advised to treat this condition.

摘要

背景与目的

外阴克罗恩病(VCD)是克罗恩病一种罕见的肠外皮肤表现。目前文献中尚未就该病的诊断检查和治疗管理达成共识。

患者与方法

对诊断并接受VCD治疗的女性患者进行回顾性、多中心描述性病例系列研究。通过查阅病历,收集初始症状、临床病程、组织学检查结果及治疗管理方面的数据。

结果

纳入15例女性患者,中位年龄28岁(四分位间距:28 - 44岁),患回肠克罗恩病(27%)、结肠克罗恩病(33%)和回结肠克罗恩病(40%)。VCD最常见的表现为外阴肿胀(93%)、疼痛(80%)和红斑(73%)。组织学分析显示,78%的病例有肉芽肿性炎症,67%的病例有混合性炎性细胞浸润。8例(53%)患者经局部治疗后外阴症状暂时减轻。免疫抑制剂与肿瘤坏死因子α抑制剂联合治疗是最有效的二线治疗方法:5例(33%)患者采用该治疗策略后实现了持续临床缓解。

结论

VCD的诊断检查具有挑战性,应采用多学科方法进行。外阴组织病理学分析有助于诊断。建议采用局部治疗以及免疫抑制剂和肿瘤坏死因子α抑制剂进行全身治疗来处理该病。

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