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白种人中肢端皮肤黑色素瘤:112例患者的临床特征、组织病理学及预后

Acral cutaneous melanoma in caucasians: clinical features, histopathology and prognosis in 112 patients.

作者信息

Kuchelmeister C, Schaumburg-Lever G, Garbe C

机构信息

Section of Dermatologic Oncology, Department of Dermatology, Eberhard-Karls-University, Liebermeisterstrasse 25, 72076 Tuebingen, Germany.

出版信息

Br J Dermatol. 2000 Aug;143(2):275-80. doi: 10.1046/j.1365-2133.2000.03651.x.

Abstract

BACKGROUND

Acral lentiginous melanoma (ALM) is the fourth distinct variant of cutaneous melanoma. The histological diagnosis and prognosis of ALM are still controversial.

OBJECTIVES

To review the features of a large series of patients with ALM, and confirm the validity of the histological criteria for this type of melanoma.

METHODS

A collection of 2642 patients with cutaneous melanoma was recorded during the period 1986-97, among these 187 were located on acral sites. Histological specimens were reviewed in 112 acral melanomas; the following study is based on this subgroup.

RESULTS

Histological examination revealed acral lentiginous melanomas predominantly in palmoplantar and subungual locations (60%), while superficial spreading melanomas (SSM) were found mainly on the dorsal aspects of hands and feet (30%). Nodular melanomas (NM) (9%) occurred in all acral sites. The histological re-examination confirmed the characteristics of ALM as described by Reed in 1976. With increasing tumour thickness nesting of tumour cells and upward migration to the cornified layer was similarly observed. The 5-year survival rate for patients with primary acral melanoma without recognizable metastasis was 82%. ALM differed significantly in survival from SSM (P = 0.001) and lentigo maligna melanoma (P < 0. 001), but survival rates were similar to NM (P = 0.9).

CONCLUSIONS

ALM, as diagnosed by current histological criteria, occur on the palms, soles and subungual sites, and have a poor prognosis.

摘要

背景

肢端雀斑样痣性黑素瘤(ALM)是皮肤黑素瘤的第四种独特亚型。ALM的组织学诊断和预后仍存在争议。

目的

回顾大量ALM患者的特征,并确认此类黑素瘤组织学标准的有效性。

方法

记录了1986 - 1997年间收集的2642例皮肤黑素瘤患者,其中187例位于肢端部位。对112例肢端黑素瘤的组织学标本进行了复查;以下研究基于该亚组。

结果

组织学检查显示,肢端雀斑样痣性黑素瘤主要位于掌跖和甲下部位(60%),而浅表扩散性黑素瘤(SSM)主要见于手足背侧(30%)。结节性黑素瘤(NM)(9%)见于所有肢端部位。组织学复查证实了1976年里德所描述的ALM特征。随着肿瘤厚度增加,同样观察到肿瘤细胞巢状排列及向上迁移至角质层。原发性肢端黑素瘤无明显转移患者的5年生存率为82%。ALM在生存率方面与SSM(P = 0.001)和恶性雀斑样痣性黑素瘤(P < 0.001)有显著差异,但生存率与NM相似(P = 0.9)。

结论

根据当前组织学标准诊断的ALM发生于手掌、足底和甲下部位,预后较差。

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