皮肤性病诊疗学杂志2023,Vol.30Issue(6) :558-560.DOI:10.3969/j.issn.1674-8468.2023.06.014

先天性丛状血管瘤1例

A case of congenital tufted angioma

何萍秀 程丽芳 吴忆 夏碧霞
皮肤性病诊疗学杂志2023,Vol.30Issue(6) :558-560.DOI:10.3969/j.issn.1674-8468.2023.06.014

先天性丛状血管瘤1例

A case of congenital tufted angioma

何萍秀 1程丽芳 1吴忆 1夏碧霞1
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作者信息

  • 1. 江西省皮肤病专科医院江西省皮肤病临床医学研究中心,江西 南昌 330001
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摘要

报告1例先天性丛状血管瘤.患者男,5岁,右肩胛部暗红色斑块5年.皮肤科检查:右肩胛部见一大小约5.0 cm ×4.0 cm暗红色浸润性斑块,表面光滑,边缘呈堤状隆起,中央凹陷于周围正常皮肤约4 mm,质硬.皮损组织病理检查:真皮全层见多个肿瘤细胞团块,由毛细血管和大小均一的梭形或类圆形内皮细胞组成,成"炮弹"样分布.免疫组织化学染色示:CD31(+),CD34(+),Ki-67(+,<1%).诊断:先天性丛状血管瘤.行皮损完整切除,随访1年半无复发.

Abstract

A case of congenital tufted angioma is reported.A 5-year-old boy presented with a dark red plaque on the right shoulder blade for 5 years.The dermatological examination showed a smooth dark-red patch of 5.0 cm ×4.0 cm in size on the right shoulder blade,with raised broders and a sunken center(4 mm deep).Histopathological examination showed lots of tumor masses composed of capillaries and cannonballs of spindle or oval endothelial cells without atypia in the dermis.Immunohistochemistry showed positive for CD31,CD34,and<1%of Ki-67 positive.The diagnosis was congenital tufted angioma.The lesion was completely excised and no recurrence was observed during the one and a half-year follow-up.

关键词

先天性/丛状/血管瘤

Key words

congenital/tufted/angioma

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基金项目

江西省皮肤病临床医学研究中心科研项目(20212BCG74003)

出版年

2023
皮肤性病诊疗学杂志
广东省皮肤性病防治中心

皮肤性病诊疗学杂志

影响因子:0.666
ISSN:1674-8468
参考文献量4
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