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斯皮茨痣(大梭形细胞和/或上皮样细胞痣)。与年龄相关的基底层上方表皮受累情况。

Spitz nevus (large spindle cell and/or epithelioid cell nevus). Age-related involvement of the suprabasal epidermis.

作者信息

Mérot Y, Frenk E

机构信息

Service de dermatologie et de vénéréologie, Centre hospitalier universitaire vaudois, Lausanne, Switzerland.

出版信息

Virchows Arch A Pathol Anat Histopathol. 1989;415(2):97-101. doi: 10.1007/BF00784346.

Abstract

The Spitz nevus (large spindle and/or epithelioid cell nevus) is a benign acquired melanocytic tumour found predominantly in children and adolescents. Depending on the architecture (junctional, compound, dermal) and cytology (predominance of spindle or epithelioid cells, or presence of both cell types) several variants have been distinguished. A histological feature occasionally leading to diagnostic difficulties is the involvement of the suprabasal epidermis. The present study details the occurrence of intraepidermal involvement (pagetoid spread, nesting of cells, trans-epidermal elimination) according to the age of the patients. 89 cases of Spitz nevus were reviewed. There were 19 compound Spitz nevi with evidence of epidermal involvement, 56 cases of compound Spitz nevi without evidence of epidermal involvement and 14 cases of dermal Spitz nevi. The epidermal involvement mainly consisted of nesting of nevus cells above the basal cell layer, 9 cases clearly showing evidence of transepidermal elimination of cell nests. Upward spread of single melanocytes (pagetoid spread) was minimal and always associated with nesting or trans-epidermal elimination. The mean age of patients was significantly lower in the group of compound nevi with intraepidermal involvement (7.16 +/- 4.52 years), than in the group of compound nevi without epidermal involvement (13.18 +/- 8.88 years). The age of the latter group was significantly lower than the group of pure intradermal nevi (30.14 +/- 11.25 years). Thus, involvement of the suprabasal epidermis is not a feature of Spitz nevi in adults; in such a case the diagnosis of malignant melanoma should be considered.

摘要

斯皮茨痣(大梭形和/或上皮样细胞痣)是一种主要在儿童和青少年中发现的良性后天性黑素细胞肿瘤。根据其结构(交界性、复合性、皮内性)和细胞学特征(梭形或上皮样细胞为主,或两种细胞类型均存在),已区分出几种变体。偶尔会导致诊断困难的一个组织学特征是基底层上方表皮受累。本研究详细阐述了根据患者年龄表皮内受累(派杰样扩散、细胞巢状排列、经表皮排出)的发生情况。回顾了89例斯皮茨痣病例。其中有19例复合性斯皮茨痣有表皮受累证据,56例复合性斯皮茨痣无表皮受累证据,14例皮内斯皮茨痣。表皮受累主要表现为痣细胞在基底细胞层上方呈巢状排列,9例清楚显示有细胞巢经表皮排出的证据。单个黑素细胞的向上扩散(派杰样扩散)极少,且总是与巢状排列或经表皮排出相关。复合性痣有表皮内受累组患者的平均年龄(7.16±4.52岁)显著低于无表皮受累的复合性痣组(13.18±8.88岁)。后一组的年龄显著低于单纯皮内痣组(30.14±11.25岁)。因此,基底层上方表皮受累不是成人斯皮茨痣的特征;在这种情况下,应考虑诊断为恶性黑色素瘤。

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