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回顾性多中心研究致命性儿科黑色素瘤。

A retrospective multicenter study of fatal pediatric melanoma.

机构信息

Harvard Medical School, Boston, Massachusetts; Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts; Boston Children's Hospital, Boston, Massachusetts.

Harvard Medical School, Boston, Massachusetts; Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.

出版信息

J Am Acad Dermatol. 2020 Nov;83(5):1274-1281. doi: 10.1016/j.jaad.2020.06.1010. Epub 2020 Jul 2.

Abstract

BACKGROUND

Pediatric melanoma is rare and diagnostically challenging.

OBJECTIVE

To characterize clinical and histopathologic features of fatal pediatric melanomas.

METHODS

Multicenter retrospective study of fatal melanoma cases in patients younger than 20 years diagnosed between 1994 and 2017.

RESULTS

Of 38 cases of fatal pediatric melanoma identified, 57% presented in white patients and 19% in Hispanic patients. The average age at diagnosis was 12.7 years (range, 0.0-19.9 y), and the average age at death was 15.6 years (range, 1.2-26.2 y). Among cases with known identifiable subtypes, 50% were nodular (8/16), 31% were superficial spreading (5/16), and 19% were spitzoid melanoma (3/16). One fourth (10/38) of melanomas arose in association with congenital melanocytic nevi.

LIMITATIONS

Retrospective nature, cohort size, and potential referral bias.

CONCLUSIONS

Pediatric melanoma can be fatal in diverse clinical presentations, including a striking prevalence of Hispanic patients compared to adult disease, and with a range of clinical subtypes, although no fatal cases of spitzoid melanoma were diagnosed during childhood.

摘要

背景

儿科黑色素瘤罕见且具有诊断挑战性。

目的

描述致命性儿科黑色素瘤的临床和组织病理学特征。

方法

对 1994 年至 2017 年间诊断的 20 岁以下致命性黑色素瘤病例进行多中心回顾性研究。

结果

确定的 38 例致命性儿科黑色素瘤中,57%的患者为白人,19%为西班牙裔。诊断时的平均年龄为 12.7 岁(范围:0.0-19.9 岁),死亡时的平均年龄为 15.6 岁(范围:1.2-26.2 岁)。在已知可识别亚型的病例中,50%为结节性(8/16),31%为浅表扩散性(5/16),19%为 Spitz 样黑色素瘤(3/16)。四分之一(10/38)的黑色素瘤与先天性黑色素细胞痣有关。

局限性

回顾性研究性质、队列规模和潜在的转诊偏倚。

结论

儿科黑色素瘤在不同的临床表现中可能是致命的,包括与成人疾病相比,西班牙裔患者的比例显著增加,以及一系列临床亚型,尽管在儿童期未诊断出致命性 Spitz 样黑色素瘤。

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