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患有BAP1相关癌症易感性综合征的家族中BAP1阴性黑素细胞肿瘤的组织形态学谱

Histomorphologic spectrum of BAP1 negative melanocytic neoplasms in a family with BAP1-associated cancer susceptibility syndrome.

作者信息

Marušić Zlatko, Buljan Marija, Busam Klaus J

机构信息

Ljudevit Jurak Department of Pathology, Clinical Hospital Center "Sestre milosrdnice", Zagreb, Croatia.

Department of Dermatology, Clinical Hospital Center "Sestre milosrdnice", Zagreb, Croatia.

出版信息

J Cutan Pathol. 2015 Jun;42(6):406-12. doi: 10.1111/cup.12493. Epub 2015 May 12.

Abstract

BACKGROUND

Multiple BAP1 negative melanocytic neoplasms are a hallmark of familial cancer susceptibility syndrome caused by BAP1 germline mutation. The syndrome is characterized by increased incidence of renal cell carcinoma, mesothelioma, cholangiocarcinoma, cutaneous and uveal melanoma and some other neoplasms.

METHODS

We report histomorphologic characteristics of six cutaneous melanocytic neoplasms with loss of BAP1 expression in two members of a family with BAP1-associated cancer susceptibility syndrome.

RESULTS

The neoplasms were dermal melanocytic nevi characterized by a proliferation of large epithelioid (spitzoid) melanocytes, and adipocytic metaplasia. Nuclear pseudoinclusions and multinucleated melanocytes were present in most neoplasms. In two of the cases, a nodular melanoma was found associated with a dermal nevus. None of the melanomas recurred or metastasized after 6 and 3 years of follow up.

CONCLUSIONS

We report two new cases of melanoma arising in a BAP1-deficient melanocytic nevus in the setting of familial tumor predisposition syndrome. Adipocytic metaplasia and nuclear pseudoinclusions may be additional morphologic clues to a BAP1-deficient nevus. It remains to be seen whether these features are more common in familial than sporadic lesions.

摘要

背景

多种BAP1阴性黑素细胞肿瘤是由BAP1种系突变引起的家族性癌症易感性综合征的标志。该综合征的特征是肾细胞癌、间皮瘤、胆管癌、皮肤和葡萄膜黑色素瘤以及其他一些肿瘤的发病率增加。

方法

我们报告了一个患有BAP1相关癌症易感性综合征的家族中两名成员的6例皮肤黑素细胞肿瘤的组织形态学特征,这些肿瘤均有BAP1表达缺失。

结果

这些肿瘤为真皮黑素细胞痣,其特征为大的上皮样(梭形样)黑素细胞增殖和脂肪化生。大多数肿瘤中存在核假包涵体和多核黑素细胞。在其中2例病例中,发现结节性黑色素瘤与真皮痣相关。经过6年和3年的随访,所有黑色素瘤均未复发或转移。

结论

我们报告了2例在家族性肿瘤易感性综合征背景下,发生于BAP1缺陷型黑素细胞痣的黑色素瘤新病例。脂肪化生和核假包涵体可能是BAP1缺陷型痣的额外形态学线索。这些特征在家族性病变中是否比散发性病变更常见,仍有待观察。

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