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儿童和青少年甲下非典型性小痣样黑素细胞增生:一项临床病理研究。

Subungual atypical lentiginous melanocytic proliferations in children and adolescents: A clinicopathologic study.

机构信息

Department of Pathology, University of Michigan, Ann Arbor, Michigan.

Department of Dermatology, University of Michigan, Ann Arbor, Michigan.

出版信息

J Am Acad Dermatol. 2018 Aug;79(2):327-336.e2. doi: 10.1016/j.jaad.2018.03.030. Epub 2018 Mar 27.

Abstract

BACKGROUND

Most subungual melanocytic lesions in children are benign, but some are difficult to classify due to prominent lentiginous growth and high-grade cytologic atypia.

OBJECTIVE

To characterize the clinicopathologic features of these rare lesions.

METHODS

Subungual atypical lentiginous melanocytic proliferations from patients <20 years of age were collected for clinical and histopathologic review. Fluorescence in situ hybridization (FISH) was performed when possible.

RESULTS

Eleven patients aged 2-19 years had expanding or darkening longitudinal pigmented streak(s) with or without Hutchinson sign. Microscopically, all revealed predominantly single-cell growth, pagetoid scatter, and poor circumscription. Eight (73%) cases showed focal or poor nesting, and 3 (27%) demonstrated confluence. Nuclear enlargement, hyperchromasia, and angulation were present in 8 (73%) cases, 7 (64%) cases, and 6 (55%) cases, respectively. One of 4 cases tested by FISH was positive. Three lesions recurred locally without other adverse outcome.

LIMITATIONS

Small sample size and short clinical follow-up. Two cases were examined in partial biopsies only.

CONCLUSION

Some subungual melanocytic lesions in children and adolescents are histologically indistinguishable from adult subungual melanoma in situ. While the biologic potential remains elusive, FISH might aid in risk stratification. Awareness of this rare group of lesions is crucial for facilitating future investigation into its biologic behavior.

摘要

背景

大多数儿童的甲下黑素细胞病变为良性,但由于存在明显的雀斑样生长和高级别细胞学异型性,有些病变难以分类。

目的

描述这些罕见病变的临床病理特征。

方法

收集了 11 名年龄在 2 至 19 岁的患者的甲下非典型性雀斑样黑素细胞增生症,进行临床和组织病理学回顾。在可能的情况下进行荧光原位杂交(FISH)。

结果

11 名患者年龄在 2 至 19 岁之间,表现为纵向色素条纹扩张或变暗,伴有或不伴有 Hutchinson 征。显微镜下,所有病变均显示主要为单细胞生长、派杰样散布和边界不良。8 例(73%)表现为局灶性或差的巢状结构,3 例(27%)表现为融合。8 例(73%)、7 例(64%)和 6 例(55%)分别显示核增大、深染和扭曲。FISH 检测的 4 例中有 1 例阳性。3 例病变局部复发,无其他不良后果。

局限性

样本量小且临床随访时间短。仅有 2 例进行了部分活检检查。

结论

一些儿童和青少年的甲下黑素细胞病变在组织学上与成人甲下原位黑色素瘤无法区分。虽然生物学潜能尚不清楚,但 FISH 可能有助于分层风险。了解这组罕见病变至关重要,有助于未来对其生物学行为进行研究。

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