Jeanne-Pasquier C, Mallet J F, Bronfen C, Minckes O, Boutard P, Comoz F, Galateau-Salle F, Rousselot P
Service d'Anatomie et Cytologie Pathologiques, 14033 Caen, Cedex.
Ann Pathol. 2001 Jun;21(3):255-8.
Angiomatoid fibrous histiocytoma is an unusual tumor, affecting primarily young adults who develop local disease with favorable prognosis. This contrasts with the aggressive natural history of malignant fibrohistiocytoma. We report case of a 9-year-old girl who presented with a tumor mass of soft tissues with an unusual deep location, thereby with non distinctive clinical features. Surgical treatment was performed.
血管样纤维组织细胞瘤是一种罕见的肿瘤,主要影响年轻成年人,他们患局部疾病,预后良好。这与恶性纤维组织细胞瘤的侵袭性自然病程形成对比。我们报告一例9岁女孩,她出现一个软组织肿瘤肿块,位置异常深,因此临床特征不明显。进行了手术治疗。