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大腿部具有棘皮瘤样和发育不良特征的非典型黑素细胞病变:29 例临床病理研究。

Atypical melanocytic lesions of the thigh with spitzoid and dysplastic features: a clinicopathologic study of 29 cases.

机构信息

Department of Pathology, Section of Dermatopathology, Medical College of Wisconsin, Milwaukee, WI, USA.

出版信息

Ann Diagn Pathol. 2013 Jun;17(3):265-9. doi: 10.1016/j.anndiagpath.2012.12.001. Epub 2013 Jan 9.

DOI:10.1016/j.anndiagpath.2012.12.001
PMID:23312707
Abstract

Melanocytic nevi in certain anatomic locations can display unusual histopathologic features potentially creating diagnostic uncertainty. Benign melanocytic nevi in sites such as acral, genital, and flexural areas may show unusual architecture and cytologic atypia, which can mimic dysplastic nevi and, sometimes, melanoma. Twenty-nine benign melanocytic skin lesions were identified in the thigh of 26 women and 3 men who showed atypical histologic features, including both dysplastic and spitzoid features. All lesions measured less than 1 cm in diameter. Eighteen cases showed features of compound nevi, and 11 were junctional. In all cases, the lesions displayed spitzoid features including large epithelioid and/or spindle cells, some melanocytes with ganglion-like cytomorphology, and focal suprabasilar upward migration. All cases showed dysplastic features. Clinical follow-up was available in 26 patients; no recurrences or metastases were observed. The demographic features and the anatomical sites of these melanocytic nevi appear to be reproducible, and in the assessment of histologically difficult cases, these data are helpful. It is our opinion that the malignant potential of these lesions with hybrid patterns (spitzoid/dysplastic) has yet to be determined, and although we favor these lesions to be benign, longer follow-up may yield a more complete understanding of their biologic potential.

摘要

某些解剖部位的黑素细胞痣可能具有不寻常的组织病理学特征,这可能会导致诊断不确定。肢端、生殖器和屈肌部位等部位的良性黑素细胞痣可能表现出不寻常的结构和细胞学异型性,这可能类似于发育不良痣,有时也类似于黑色素瘤。在 26 名女性和 3 名男性的大腿上发现了 29 个良性黑素细胞皮肤病变,这些病变表现出不典型的组织学特征,包括发育不良和 Spitz 样特征。所有病变的直径均小于 1 厘米。18 例显示复合痣特征,11 例为交界痣。在所有病例中,病变均显示 Spitz 样特征,包括大的上皮样和/或梭形细胞、一些具有神经节样细胞形态的黑素细胞,以及局灶性基底上方向上迁移。所有病例均显示发育不良特征。在 26 例患者中可获得临床随访;未观察到复发或转移。这些黑素细胞痣的人口统计学特征和解剖部位似乎是可重复的,在评估组织学上困难的病例时,这些数据很有帮助。我们认为这些具有混合模式(Spitz 样/发育不良)的病变的恶性潜能尚未确定,尽管我们倾向于认为这些病变是良性的,但更长时间的随访可能会更全面地了解其生物学潜能。

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