Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
The Ronald O. Perelman Department of Dermatology, NYU Grossman School of Medicine, New York, New York, USA.
Pediatr Dermatol. 2024 Sep-Oct;41(5):807-813. doi: 10.1111/pde.15689. Epub 2024 Jul 16.
Cutaneous (or "Metastatic") Crohn disease (CCD) is a rare and underrecognized disease characterized by cutaneous granulomatous inflammation. We describe patient demographics, clinical characteristics, histology, and treatment of 89 pediatric cases of CCD, including 78 previously reported and 11 new cases seen at four academic institutions. We emphasize the efficacy of biologic mono- and dual therapy.
PubMed identified cases using keywords including "metastatic Crohn disease" and "cutaneous Crohn disease". Patients were identified by retrospective review of the electronic health record including histopathologic diagnosis consistent with CCD. Chart review collected demographic, clinical, and histologic data.
Most pediatric patients with CCD are male 55% (49/89), present with edema (73/89, 82%) and erythema (47/89, 53%) of the genitals (33/49, 67%), and have intestinal Crohn disease (69/89, 78%). Oral corticosteroids (53/75, 71%) and metronidazole (29/75, 39%) are the most frequently prescribed medications. Of the 17 patients treated with tumor necrosis factor (TNF)-blockade, 94% (16/17) had partial or total clearance. Ustekinumab resulted in clearance of cutaneous disease in two patients (2/3, 67%) and partial clearance in one patient (1/3, 33%). Two cases achieved total clearance with the use of dual biologic therapy defined as the use of two biologic therapies with differing mechanisms of action or the use of a biologic therapy and small molecule inhibitor.
TNF blockade is an effective treatment for pediatric CCD, and interleukin-12/23 inhibitors may be similarly effective. Consideration of dual biologic therapy may be useful in pediatric patients requiring discordant therapies for their intestinal and cutaneous CD.
皮肤(或“转移性”)克罗恩病(CCD)是一种罕见且未被充分认识的疾病,其特征为皮肤肉芽肿性炎症。我们描述了 89 例儿科 CCD 患者的人口统计学、临床特征、组织学和治疗情况,包括 78 例先前报告的病例和在四个学术机构中发现的 11 例新病例。我们强调生物单药和双联治疗的疗效。
使用包括“转移性克罗恩病”和“皮肤克罗恩病”在内的关键词在 PubMed 上搜索病例。通过电子病历的回顾性分析确定患者,包括符合 CCD 的组织病理学诊断。通过图表回顾收集人口统计学、临床和组织学数据。
大多数患有 CCD 的儿科患者为男性(55%,49/89),表现为生殖器肿胀(73/89,82%)和红斑(47/89,53%),并且患有肠道克罗恩病(69/89,78%)。最常开的药物是口服皮质类固醇(53/75,71%)和甲硝唑(29/75,39%)。17 例接受肿瘤坏死因子(TNF)阻滞剂治疗的患者中,94%(16/17)有部分或完全缓解。乌司奴单抗使两例(2/3,67%)患者的皮肤疾病完全清除,一例(1/3,33%)患者部分清除。两例患者使用两种不同作用机制的生物制剂或生物制剂联合小分子抑制剂的双重生物治疗实现了完全清除。
TNF 阻滞剂是儿科 CCD 的有效治疗方法,白细胞介素-12/23 抑制剂可能同样有效。对于需要对其肠道和皮肤 CD 进行不同治疗的儿科患者,考虑双重生物治疗可能是有用的。