肢端皮肤血管骨瘤：1例罕见病例。
Acral angioosteoma cutis: A rare case.
作者信息
Erdogan-Durmus Senay, Ozekinci Selver, Yarikkaya Enver, Erzurumluoglu Nurhan
机构信息
Department of Pathology, Erzurum Region Training and Research Hospital, Erzurum, Turkey.
Department of Pathology, Okmeydanı Training and Research Hospital, İstanbul, Turkey.
出版信息
Indian J Dermatol Venereol Leprol. 2018 Nov-Dec;84(6):685-686. doi: 10.4103/ijdvl.IJDVL_117_17.
Acral angioosteoma cutis is a rare and benign cutaneous lesion clinically characterized by an exophytic growth resembling pyogenic granuloma on the acral skin; first described in 2006. Its pathogenesis is still unclear while well-formed capillaries, pale stroma, bland fibroblast-like cells, and multiple tiny spicules of woven bone constitute the histological hallmarks. Here, we present a case of acral angioosteoma cutis in a 34-year-old man to increase awareness regarding this rare condition.
肢端皮肤血管骨瘤是一种罕见的良性皮肤病变，临床特征为肢端皮肤出现类似化脓性肉芽肿的外生性生长；于2006年首次被描述。其发病机制尚不清楚，而形态良好的毛细血管、淡染的间质、温和的成纤维细胞样细胞以及多个编织骨小刺构成了组织学特征。在此，我们报告一例34岁男性的肢端皮肤血管骨瘤病例，以提高对这种罕见疾病的认识。
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