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单纯型大疱性表皮松解症基础上发生的恶性黑素瘤:与大疱性表皮松解痣的重要区别。

Malignant melanoma arising in the setting of epidermolysis bullosa simplex: an important distinction from epidermolysis bullosa nevus.

机构信息

Department of Pathology, University of Michigan, Ann Arbor.

出版信息

JAMA Dermatol. 2013 Oct;149(10):1195-8. doi: 10.1001/jamadermatol.2013.4833.

Abstract

IMPORTANCE

Patients with epidermolysis bullosa (EB) do not carry a significantly increased risk of melanoma but are prone to developing large, markedly atypical melanocytic nevi (EB nevi), which may mimic melanoma clinically and histologically. Many authors now favor a conservative approach in managing atypical pigmented lesions in patients with EB.

OBSERVATIONS

We present the case of a 30-year-old woman with severe EB simplex who sought care for a large red and black ulcerated plaque. The clinical differential diagnosis included EB nevus and melanoma. An incisional punch biopsy specimen revealed an atypical melanocytic proliferation with focal florid pagetoid spread and involving elongated rete ridges, consistent with invasive acral lentiginous melanoma. The subsequent amputation was confirmatory. Micrometastasis was detected in 1 of 5 sentinel lymph nodes.

CONCLUSIONS AND RELEVANCE

To our knowledge, this is the first reported case of melanoma arising in EB simplex-affected skin. It highlights the difficulty in differentiating melanoma from an EB nevus. Despite the increasing awareness of EB nevi, a high index of suspicion for melanoma should be maintained, and early biopsy is recommended when evaluating large pigmented lesions in patients with EB.

摘要

重要性

患有大疱性表皮松解症(EB)的患者患黑色素瘤的风险并不显著增加,但易发生大而显著非典型性黑色素细胞痣(EB 痣),这些痣在临床上和组织学上可能类似于黑色素瘤。现在,许多作者倾向于对 EB 患者的非典型色素性病变采取保守的处理方法。

观察结果

我们报告了一例 30 岁的单纯性 EB 女性患者,因一个大的红色和黑色溃疡性斑块就诊。临床鉴别诊断包括 EB 痣和黑色素瘤。一个切开性打孔活检标本显示出非典型性黑色素细胞增生,伴有局灶性华丽的派杰样扩散,并累及拉长的网嵴,符合侵袭性肢端雀斑样黑色素瘤。随后的截肢术得到了证实。在 5 个前哨淋巴结中,有 1 个发现了微转移。

结论和相关性

据我们所知,这是首例报告的发生在单纯性 EB 皮肤的黑色素瘤病例。它强调了区分黑色素瘤与 EB 痣的困难。尽管对 EB 痣的认识不断提高,但在评估 EB 患者的大色素性病变时,应保持对黑色素瘤的高度怀疑,并建议早期进行活检。

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