Ro J Y, Ayala A G, Ordóñez N G, Swanson D A, Babaian R J
Am J Clin Pathol. 1986 Nov;86(5):583-90. doi: 10.1093/ajcp/86.5.583.
The light-microscopic, immunohistochemical, and ultrastructural features of two examples of a pseudosarcomatous fibromyxoid tumor of the urinary bladder are reported. Both patients were women, 56 and 52 years old. Gross hematuria was the chief complaint and occurred for two days and two weeks, respectively, before presentation. Cystoscopy revealed a 2 X 1 X 1 cm mass located at the dome in case 1 and a 4 X 3 X 3 cm mass at the left posterior lateral wall in case 2. Microscopically, the lesions were composed of spindle, plump, or stellated fibroblast-like cells embedded in myxoid stroma with little collagen; mitotic figures were about 2 per 10 high-power fields, and both cases showed encroachment of the superficial muscle bundles. Because of bizarre spindle cell proliferation, occasional mitoses, and invasion to the underlying muscle, these lesions were initially diagnosed as embryonal rhabdomyosarcoma. However, follow-up examination disclosed the benign nature of these lesions. There was no previous instrumentation or surgery on the genitourinary tract. Immunohistochemical and ultrastructural studies revealed the fibroblastic-myofibroblastic nature of these lesions. These cases illustrate that clinicopathologic correlation is essential to define certain pseudosarcomatous lesions.
报道了两例膀胱假肉瘤性纤维黏液样肿瘤的光镜、免疫组化及超微结构特征。两名患者均为女性,年龄分别为56岁和52岁。主要症状为肉眼血尿,分别在就诊前2天和2周出现。膀胱镜检查显示,病例1中一个2×1×1 cm的肿块位于膀胱顶部,病例2中一个4×3×3 cm的肿块位于左后外侧壁。显微镜下,病变由梭形、丰满或星状的成纤维细胞样细胞组成,嵌入黏液样基质中,胶原极少;每10个高倍视野中有约2个有丝分裂象,两例均显示浅表肌束受侵犯。由于怪异的梭形细胞增生、偶见的有丝分裂及对下方肌肉的侵犯,这些病变最初被诊断为胚胎性横纹肌肉瘤。然而,随访检查显示这些病变为良性。既往无泌尿生殖道器械检查或手术史。免疫组化及超微结构研究显示这些病变具有成纤维细胞-肌成纤维细胞性质。这些病例表明,临床病理相关性对于某些假肉瘤性病变的诊断至关重要。