Perineuriomatous Melanocytic Nevi: A Case Series of Four Cases.

IF 1.6 4区 医学 Q3 DERMATOLOGY
Aya Almashad, Miki Lindsey, Nicholas Zoumberos, Sara C Shalin
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Abstract

Background: Melanocytic tumors with perineuriomatous differentiation may pose diagnostic challenges. This study explores characteristics of perineuriomatous melanocytic nevi, an entity merging features of perineurioma and melanocytic nevi. The aim is to elucidate histopathological features of perineuriomatous nevi to allow dermatopathologists to recognize them and differentiate them from other spindle cell lesions.

Method: This study reviews four cases (2020-2023) of melanocytic nevi with perineuriomatous components.

Results: All cases comprised adults (median age: 64.50, mean age: 60.25), with a female predominance, and exhibited clinical features characterized by irregular brown macules or papules on the trunk and extremities. Histopathologically, all lesions were compound, and biphasic patterns were evident, encompassing superficial nevoid and deeper spindled populations arranged in whorled fascicles and embedded in a sclerotic or myxoid stroma. Immunohistochemistry revealed expression of at least one perineuriomatous marker in deeper cells. Cases were assessed and compared with previously published cases for comprehensive insights. Three of our four cases demonstrated the presence of a junctional component that was smaller than the dermal component. We suggest that this unusual feature, which we term the "reverse shoulder", may allow dermatopathologists to help consider perineurial differentiation in the appropriate setting.

Conclusion: Perineuriomatous nevi can pose diagnostic challenges. This study contributes to the growing body of literature on perineuriomatous nevi, emphasizing their unique features and the importance of accurate diagnosis to avoid unnecessary interventions.

毛周黑素细胞痣:四例病例系列
背景:会厌分化的黑色素细胞肿瘤可能会给诊断带来挑战。本研究探讨了会厌黑色素细胞痣的特征,这是一种融合了会厌瘤和黑色素细胞痣特征的实体。目的是阐明会厌痣的组织病理学特征,以便皮肤病理学家识别它们,并将它们与其他纺锤形细胞病变区分开来:本研究回顾了四例(2020-2023年)具有会厌瘤成分的黑素细胞痣:所有病例均为成年人(中位年龄:64.50岁,平均年龄:60.25岁),女性居多,临床特征为躯干和四肢出现不规则的棕色斑丘疹或丘疹。从组织病理学角度看,所有病变均为复合型,双相模式明显,包括表层的痣状和深层的纺锤形群体,呈轮状束状排列,嵌入硬化或肌样基质中。免疫组化结果显示,深层细胞中至少有一种瘤周标志物的表达。我们对病例进行了评估,并与以前发表的病例进行了比较,以获得全面的认识。在我们的四个病例中,有三个病例的交界部分比真皮部分小。我们认为,这种不寻常的特征(我们称之为 "反向肩")可能有助于皮肤病理学家在适当的情况下考虑会阴分化:结论:会厌痣会给诊断带来挑战。本研究为不断增加的会阴瘤样痣文献做出了贡献,它强调了会阴瘤样痣的独特特征和准确诊断的重要性,以避免不必要的干预。
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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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