Multinucleate cell angiohistiocytoma of the upper lip

Anne Cale Jones DDS (Assistant Professor) , Diane Mullins MD (Assistant Professor) , Felix Jimenez DDS (Private Practice)
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引用次数: 23

Abstract

Multinucleate cell angiohistiocytoma is a rare benign fibrohistiocytic vascular tumor with distinctive histologic features. It appears clinically as small, slow-growing, grouped reddish-brown to purple papules and nodules that may be mistaken for other vascular proliferative or reactive conditions. Multinucleate cell angiohistiocytoma tends to occur more frequently in women, to favor the extremities, and to appear as multiple lesions. We report a case of a solitary multinucleate cell angiohistiocytoma that appeared as a nodule on the upper lip of a man but that otherwise demonstrated characteristic histologic and immunohistochemical features. Greater awareness of this uncommon benign lesion will facilitate diagnosis and appropriate management.

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上唇多核细胞血管组织细胞瘤
多核细胞血管组织细胞瘤是一种罕见的良性纤维组织细胞血管肿瘤,具有独特的组织学特征。临床表现为小的、生长缓慢的、成组的红棕色到紫色丘疹和结节,可能被误认为是其他血管增生或反应性疾病。多核细胞血管组织细胞瘤多发于女性,多发于四肢,并表现为多发病变。我们报告一例孤立的多核细胞血管组织细胞瘤,表现为男性上唇的结节,但其他方面表现出典型的组织学和免疫组织化学特征。提高对这种罕见良性病变的认识将有助于诊断和适当的治疗。
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