[腹腔内硬纤维瘤]

[Intra-abdominal desmoid tumor].

作者信息

González M A, Menéndez R, Ayala J M, Herrero M, Cuesta J, Domínguez A, Martínez M, Graña J L, Pozo F

机构信息

Servicio de Cirugía General y del Aparato Digestivo, Hospital Vital Alvarez-Buylla, Mieres, Asturias, España.

出版信息

Cir Esp. 2005 Jun;77(6):362-4. doi: 10.1016/s0009-739x(05)70872-1.

DOI:10.1016/s0009-739x(05)70872-1

PMID:16420952

Abstract

Aggressive fibromatosis (desmoid tumor) are rare connective tissue tumors that occur sporadically or in association with familial adenomatous polyposis. The etiology is unknown and clinical findings depend on growth into neighboring structures. Biopsy is required to establish the diagnosis. The treatment of choice is surgery. We report a case with unusual localization in this form of presentation. The patient remains asymptomatic 15 months after surgery.

摘要

侵袭性纤维瘤病（韧带样瘤）是一种罕见的结缔组织肿瘤，可散发出现或与家族性腺瘤性息肉病相关。其病因不明，临床表现取决于肿瘤向邻近结构的生长情况。需要通过活检来确诊。首选治疗方法是手术。我们报告了一例以这种表现形式出现的异常定位病例。该患者术后15个月仍无症状。