Jafarian Fatemeh, McCuaig Catherine, Kokta Victor, Laberge Louise, Ben Nejma Bourouia
Division of Dermatology, Department of Pediatrics, Sainte-Justine Hospital, University of Montreal, Montreal, Quebec, Canada.
Pediatr Dermatol. 2008 May-Jun;25(3):317-25. doi: 10.1111/j.1525-1470.2008.00674.x.
We reviewed all occurrences of dermatofibrosarcoma protuberans in children under 17 years of age who were evaluated at Sainte-Justine Hospital, a tertiary-care pediatric center, between 1980 and 2002. The medical records and histologic features of all were reviewed. Eight patients were identified, three boys and five girls. The interval between apparent onset and diagnosis ranged from 3 months to 14 years. All lesions except one were removed by surgical excision with a margin of 1.5 to 3 cm including underlying fascia or by Mohs technique. Follow-up ranged from 2 to 15 years with median of 5 years. To date all the patients are alive and none has had a recurrence.
我们回顾了1980年至2002年间在三级儿科中心圣贾斯汀医院接受评估的17岁以下儿童发生的所有隆突性皮肤纤维肉瘤病例。对所有病例的病历和组织学特征进行了回顾。共识别出8例患者,3名男孩和5名女孩。从明显发病到诊断的间隔时间为3个月至14年。除1例病变外,所有病变均通过手术切除,切缘为1.5至3厘米,包括深部筋膜,或采用莫氏手术技术切除。随访时间为2至15年,中位随访时间为5年。迄今为止,所有患者均存活,无一例复发。