先天性黑素细胞痣合并神经性皮肤错构瘤1例。

IF 1.6 Q3 DERMATOLOGY
Dina El-Rayes, Katlin Wilson, Sheilagh Maguiness, Daniel Miller, Gerardo Cazzato, Alessio Giubellino
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引用次数: 0

摘要

先天性黑素细胞痣(CMN)是出生时或出生后几个月出现的良性肿瘤。这些痣的一小部分表现为轻度非典型特征和异质性分化,包括许旺氏分化。我们报告一个3周大的病例,7厘米的红色/紫色头皮结节与CMN一致,伴有轻度非典型异质区。在组织学上,纤维基质中可见梭形细胞的真皮巢,血管增多,胶原束之间和附件结构周围散布着小的圆形黑色素细胞簇。病变也表现出罕见的黑素细胞呈单细胞和巢状上升。总的来说,这些特征与CMN合并结节性增生性神经性皮肤错构瘤(NCH)一致,并伴有轻度非典型黑素细胞增殖的复合成分。下一代测序(NGS)鉴定了一种新的SH2B1::BRAF融合。本病例强调了在幼儿CMN中异质分化的诊断挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital Melanocytic Nevus with Neurocristic Cutaneous Hamartoma: A Case Report.

Congenital melanocytic nevi (CMN) are benign tumors present at birth or arising in the first few months of life. A small subset of these nevi present with mild atypical features and heterogeneous differentiation, including Schwannian differentiation. We present a case of a 3-week-old with a 7 cm red/purple scalp nodule consistent with CMN with mild atypical heterogeneous areas. On histology, there were dermal nests of spindle cells in a fibrillar matrix, with increased vessels and clusters of small round melanocytes interspersed between collagen bundles and around adnexal structures. The lesion also exhibited rare pagetoid ascent of melanocytes as single cells and nests. Overall, these features were consistent with a CMN with nodular proliferative neurocristic cutaneous hamartoma (NCH) with a component of a compound mild atypical melanocytic proliferation. Next generation sequencing (NGS) identified a novel SH2B1::BRAF fusion. This case highlights the diagnostic challenges of heterogeneous differentiation within CMN in young children.

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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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