Suster S, Nascimento A G, Miettinen M, Sickel J Z, Moran C A
Arkadi M. Rywlin Department of Pathology & Laboratory Medicine, Mount Sinai Medical Center, Miami Beach, FL 33140, USA.
Am J Surg Pathol. 1995 Nov;19(11):1257-66. doi: 10.1097/00000478-199511000-00005.
We describe 12 cases of primary soft tissue neoplasms that showed the histologic and immunohistochemical features of solitary fibrous tumors of serosal surfaces (solitary fibrous mesothelioma, submesothelial fibroma). Nine patients were women and three were men whose ages ranged from 28 to 83 years. Seven lesions were located in the head and neck region, and the remainder were located in the back, buttock, perineum, and groin. The lesions measured from 1 to 6 cm in greatest diameter and presented grossly as well-circumscribed, unencapsulated, soft to rubbery tissue masses. Histologically they were characterized by a proliferation of spindle cells exhibiting a variety of growth patterns, including storiform, herringbone, neural with wavy nuclei, and hemangiopericytic admixed with areas of sclerosis. In two cases the lesions showed areas of increased cellularity with occasionally scattered mitotic figures. Three cases were located adjacent to a major salivary gland; in one, entrapment of normal salivary gland acini and ducts could be observed at the edges of the lesion. Immunohistochemical studies showed positive staining of the spindle cells with CD34 (anti-HPCA-1) and vimentin antibodies and negative staining with keratin, actin, desmin, S-100 protein, collagen type IV, and factor VIII related antigen. Follow-up from 6 months to 12 years has shown no evidence of recurrence or metastasis in any of our patients. Solitary fibrous tumors appear to represent ubiquitous mesenchymal neoplasms that may not be necessarily restricted to serosal surfaces. Identification of these lesions is of importance to avoid misdiagnosis with other more aggressive conditions in soft tissue locations.
我们描述了12例原发性软组织肿瘤,其具有浆膜表面孤立性纤维瘤(孤立性纤维性间皮瘤、间皮下纤维瘤)的组织学和免疫组化特征。9例患者为女性,3例为男性,年龄范围为28至83岁。7个病变位于头颈部区域,其余位于背部、臀部、会阴和腹股沟。病变最大直径为1至6厘米,大体表现为边界清楚、无包膜、质地软至橡胶样的组织块。组织学上,其特征为梭形细胞增生,呈现多种生长模式,包括漩涡状、人字形、核呈波浪状的神经样以及与硬化区域混合的血管外皮细胞瘤样。2例病变显示细胞增多区域,偶见散在的有丝分裂象。3例病变位于大唾液腺附近;其中1例在病变边缘可观察到正常唾液腺腺泡和导管被包绕。免疫组化研究显示梭形细胞对CD34(抗HPCA-1)和波形蛋白抗体呈阳性染色,对角蛋白、肌动蛋白、结蛋白、S-100蛋白、IV型胶原和VIII因子相关抗原呈阴性染色。随访6个月至12年,我们所有患者均无复发或转移迹象。孤立性纤维瘤似乎代表普遍存在的间叶性肿瘤,不一定局限于浆膜表面。识别这些病变对于避免在软组织部位与其他更具侵袭性的疾病误诊很重要。