Lee J R, Hancock S M, Martindale R G
Department of Pathology, Veterans Affairs Medical Center, and Institute of Molecular Medicine and Genetics, Medical College of Georgia, Augusta 30904, USA.
Am Surg. 2001 Jun;67(6):577-81.
Solitary fibrous tumor (SFT) of the peritoneum is an unusual spindle-cell neoplasm. SFT was originally described in the pleura; however it is now diagnosed in multiple extrathoracic sites. Most believe that the tumor is of mesenchymal origin and should be classified as a variant of fibroma. SFT of the pleura and peritoneum have also been called fibrous mesothelioma, and the cell of origin is felt to be a pluripotential submesothelial mesenchymal cell. Primary tumors arising in hernia sacs are rare, and we report on two patients with hernia SFT. The first is a 67-year-old man who had a diffusely thickened distal left inguinal hernia sac. Within the sac was copious myxoid material mimicking pseudomyxoma peritonei. Herniorrhaphy and orchiectomy were performed. The second is a 44-year-old woman with a midepigastric mass attached to a ventral hernia. Wide local excision was performed. Both tumors demonstrated plump spindle cells, one with myxoid background and the other with keloidal collagen. Calretinin immunostaining was positive in both tumors, whereas CD34 was negative. This suggests tumor origin from a submesothial pluripotential cell that maintains potential for mesothelial differentiation. Surgical excision is the treatment of choice with the degree of resectability being a powerful predictor of outcome.
腹膜孤立性纤维性肿瘤(SFT)是一种罕见的梭形细胞瘤。SFT最初在胸膜中被描述;然而,现在在多个胸外部位都有诊断。大多数人认为该肿瘤起源于间充质,应归类为纤维瘤的一种变体。胸膜和腹膜的SFT也被称为纤维性间皮瘤,其起源细胞被认为是一种多能的间皮下间充质细胞。疝囊内发生的原发性肿瘤很少见,我们报告了两例疝SFT患者。第一例患者是一名67岁男性,左侧腹股沟疝囊远端弥漫性增厚。囊内有大量黏液样物质,类似腹膜假黏液瘤。进行了疝修补术和睾丸切除术。第二例患者是一名44岁女性,中腹部有一肿块附着于腹疝。进行了广泛的局部切除。两个肿瘤均显示丰满的梭形细胞,一个有黏液样背景,另一个有瘢痕疙瘩样胶原。钙视网膜蛋白免疫染色在两个肿瘤中均为阳性,而CD34为阴性。这表明肿瘤起源于间皮下多能细胞,该细胞保持着间皮分化的潜能。手术切除是首选的治疗方法,可切除程度是预后的有力预测指标。