Blue Nevus-Like Metastatic Melanoma in a Patient With Primary Lentigo Maligna Melanoma.

IF 1.6 4区 医学 Q3 DERMATOLOGY
Kristen Fernandez, Mitul B Modi, Jodi J Speiser
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引用次数: 0

Abstract

Metastatic melanoma with unusual histopathology can be diagnostically challenging. One exceptionally rare cutaneous manifestation of metastases is blue-nevus-like metastatic melanoma (BNLMM). A 74-year-old male presented with a blue-gray lesion on his left helix in the same anatomical region of a previously resected lentigo maligna. Histopathological sections demonstrated an atypical biphasic proliferation of dendritic melanocytes with pigment incontinence and epidermal sparing, measuring > 0.05 mm in diameter. Although the majority of the cell population exhibited cytologic features consistent with a blue nevus, there was a subset of dendritic cells with irregular epithelioid contours and rare, typical dermal mitotic figures. Sections showed an increased Mart-1/Ki67 rate. Perineural and angiotropic involvement by the atypical melanocytes was identified. Immunohistochemical (IHC) stains for SOX-10, HMB45, and PRAME highlighted melanocytic proliferation. BAP-1 IHC was retained, and p16 IHC showed complete loss. No previous procedure site changes were present, indicating that the dendritic cell proliferation was separated from the primary invasive melanoma by normal dermis. The histopathological and immunohistochemical findings led to a diagnosis of microsatellite BNLMM. We report this case to highlight the importance of this rare entity and to avoid misdiagnosis of BNLMM, which would significantly impact patient prognosis, treatment, follow-up, and outcomes.

原发性黄斑性恶性黑色素瘤患者的蓝色痣样转移性黑色素瘤。
具有异常组织病理学的转移性黑色素瘤可能具有诊断挑战性。一种非常罕见的皮肤转移表现是蓝痣样转移性黑色素瘤(BNLMM)。一个74岁的男性提出了一个蓝灰色病变在他的左螺旋在相同的解剖区域以前切除的恶性晶状体。组织病理切片显示树突状黑色素细胞非典型双期增生,伴色素失禁和表皮保留,直径约0.05 mm。虽然大多数细胞群表现出与蓝色痣一致的细胞学特征,但也有一部分树突状细胞具有不规则的上皮样轮廓和罕见的典型真皮有丝分裂象。切片显示Mart-1/Ki67率升高。发现非典型黑色素细胞累及神经周围和血管增生。免疫组化(IHC)染色显示SOX-10、HMB45和PRAME的黑色素细胞增殖。BAP-1 IHC保留,p16 IHC完全丢失。先前的手术部位没有改变,表明树突状细胞增生是通过正常真皮从原发性侵袭性黑色素瘤中分离出来的。组织病理学和免疫组织化学检查结果诊断为微卫星型BNLMM。我们报告这个病例是为了强调这种罕见的实体的重要性,并避免误诊BNLMM,这将显著影响患者的预后,治疗,随访和结果。
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来源期刊
CiteScore
3.20
自引率
5.90%
发文量
174
审稿时长
3-8 weeks
期刊介绍: Journal of Cutaneous Pathology publishes manuscripts broadly relevant to diseases of the skin and mucosae, with the aims of advancing scientific knowledge regarding dermatopathology and enhancing the communication between clinical practitioners and research scientists. Original scientific manuscripts on diagnostic and experimental cutaneous pathology are especially desirable. Timely, pertinent review articles also will be given high priority. Manuscripts based on light, fluorescence, and electron microscopy, histochemistry, immunology, molecular biology, and genetics, as well as allied sciences, are all welcome, provided their principal focus is on cutaneous pathology. Publication time will be kept as short as possible, ensuring that articles will be quickly available to all interested in this speciality.
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