Pattee S F, Hansen R C, Bangert J L, Joganic E F
Section of Dermatology, University of Arizona College of Medicine, Tucson, Arizona, USA.
Pediatr Dermatol. 2001 Jul-Aug;18(4):320-4. doi: 10.1046/j.1525-1470.2001.01938.x.
Giant congenital melanocytic nevi are a rare occurrence in the pediatric population. The risk of malignant transformation associated with these lesions has been well established; however, the management strategies for giant congenital nevi remain controversial. We report an unusual sclerodermoid reaction in a giant congenital nevus in a 6-week-old Caucasian girl. Given its abnormal clinical appearance, the entire lesion was excised. The histology was consistent with an atypical compound/sclerosing spindle and epithelioid cell congenital nevus. No evidence of malignant change was seen histologically. The incidence of malignant transformation in giant congenital nevi has been difficult to calculate. Review of the literature yields an incidence of between 4 and 9%, favoring surgical excision of these lesions where possible. Atypical presentations of giant congenital nevi are rare, and we have found no other reported cases with a stromal change similar to that seen in our patient. We hypothesize that this change may represent an atypical host reaction to the nevus cells.
巨大先天性黑素细胞痣在儿科人群中较为罕见。与这些病变相关的恶性转化风险已得到充分证实;然而,巨大先天性痣的管理策略仍存在争议。我们报告了一名6周大的白种女孩巨大先天性痣中出现的一种不寻常的硬皮病样反应。鉴于其异常的临床表现,整个病变被切除。组织学检查结果与非典型复合性/硬化性梭形和上皮样细胞先天性痣一致。组织学上未见恶性改变的证据。巨大先天性痣的恶性转化率很难计算。文献回顾显示其发生率在4%至9%之间,因此在可能的情况下倾向于对这些病变进行手术切除。巨大先天性痣的非典型表现很少见,我们未发现其他报道的病例有与我们患者所见类似的间质改变。我们推测这种改变可能代表了宿主对痣细胞的一种非典型反应。