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巨大先天性蓝色痣表现为脑回状头皮:病例报告及文献复习。

Giant Congenital Blue Nevus Presenting as Cutis Verticis Gyrata: A Case Report and Review of the Literature.

机构信息

School of Medicine, University of Kansas, Kansas City, KS, USA.

Department of Pathology, University of Kansas, Kansas City, KS, USA.

出版信息

Ann Otol Rhinol Laryngol. 2021 Dec;130(12):1407-1411. doi: 10.1177/00034894211007236. Epub 2021 Apr 3.

DOI:10.1177/00034894211007236
PMID:33813872
Abstract

OBJECTIVES

Cerebriform intradermal nevus and giant congenital blue nevi are rarely reported melanocytic nevi with clinical and histopathologic similarities. Both are known to produce cutis verticis gyrata. We report a significantly large occipital scalp congenital blue nevus with secondary cutis verticis gyrata. The aim of this report is to increase clinical awareness of this entity, highlight histopathologic and mutational features of cerebriform intradermal nevi and giant congenital blue nevi, and stress the importance of clinicopathologic correlation for diagnosis.

METHODS

Case report and review of the literature.

RESULTS

A 20-year-old Asian male presented with a long-standing, large (20 cm × 30 cm), exophytic tumor at the occipital scalp and posterior neck. The skin overlying the lesion was arranged in thick folds resembling the surface of the brain, devoid of hair follicles, and discolored by salt-and-pepper pattern hyperpigmentation. After correlating the clinical and histopathologic findings, we diagnosed giant congenital blue nevus with secondary cutis verticis gyrata. Staged surgical excision was performed with subsequent treatment for hypertrophic scarring and occipital alopecia.

CONCLUSIONS

Cerebriform intradermal nevus and giant congenital blue nevus have overlapping histologic and clinical features. Head and neck surgeons should be aware that nomenclature of these tumors is subjective and often imprecise. Diagnosis requires correlation of clinical findings, patient history, and histopathology. Surgical excision is advised due to rare malignant transformation potential.

摘要

目的

脑回状真皮内痣和巨大先天性蓝色痣是罕见的具有临床和组织病理学相似性的黑色素瘤。两者均已知会产生脑回状头皮。我们报告了一例枕部头皮巨大先天性蓝色痣伴继发性脑回状头皮。本报告的目的是提高对该实体的临床认识,强调脑回状真皮内痣和巨大先天性蓝色痣的组织病理学和突变特征,并强调临床病理相关性对诊断的重要性。

方法

病例报告和文献复习。

结果

一名 20 岁的亚裔男性,其枕部头皮和后颈部有一个长期存在的、大的(20cm×30cm)外生性肿瘤。病变上方的皮肤呈厚褶皱状,类似于大脑表面,无毛囊,呈椒盐样色素沉着。在将临床和组织病理学发现相关联后,我们诊断为巨大先天性蓝色痣伴继发性脑回状头皮。进行了分期手术切除,随后对肥厚性瘢痕和枕部脱发进行了治疗。

结论

脑回状真皮内痣和巨大先天性蓝色痣具有重叠的组织学和临床特征。头颈部外科医生应该意识到这些肿瘤的命名是主观的,而且往往不准确。诊断需要将临床发现、患者病史和组织病理学进行关联。由于罕见的恶性转化潜力,建议进行手术切除。

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Ann Otol Rhinol Laryngol. 2021 Dec;130(12):1407-1411. doi: 10.1177/00034894211007236. Epub 2021 Apr 3.
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