Cummings T J, Liu K, Jordan L K, Dodd L G
Department of Pathology and Cytopathology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Diagn Cytopathol. 2000 Jul;23(1):55-8. doi: 10.1002/1097-0339(200007)23:1<55::aid-dc13>3.0.co;2-b.
A 51-yr-old male presented with an 8-mo history of lower back pain. Computerized axial tomography (CT) and magnetic resonance imaging (MRI) studies showed a 3.5 X 3.0 cm sacral mass within the spinal canal in the region of the left S2 nerve root. A fine-needle aspirate biopsy (FNAB) was performed under CT guidance. The cytologic findings included a spindle-cell population with a fibrillary background arranged in a vaguely streaming pattern, wavy nuclei with mild atypia, wispy cytoplasm, rare intranuclear inclusions, and dilated vascular spaces. Some cells contained a nonrefractile granular brown pigment consistent with melanin. Also identified were calcified concentric laminations typical of psammoma bodies. Immunohistochemically, the neoplastic cells were strongly immunoreactive for S-100 protein and HMB-45. A diagnosis of psammomatous melanotic schwannoma was rendered. No stigmata of Carney's complex were identified on physical examination. The patient has declined the recommendation of surgical excision of the mass. We herein describe a case unequivocally diagnosed as psammomatous melanotic schwannoma by FNAB.
一名51岁男性,有8个月的下背部疼痛病史。计算机断层扫描(CT)和磁共振成像(MRI)检查显示,在左侧S2神经根区域的椎管内有一个3.5×3.0厘米的骶骨肿物。在CT引导下进行了细针穿刺抽吸活检(FNAB)。细胞学检查结果包括:有梭形细胞群,其纤维背景呈模糊的束状排列,细胞核呈波浪状,有轻度异型性,细胞质纤细,罕见核内包涵体,血管间隙扩张。一些细胞含有与黑色素一致的非折光性颗粒状棕色色素。还发现了砂粒体典型的钙化同心层。免疫组织化学检查显示,肿瘤细胞对S-100蛋白和HMB-45呈强免疫反应。诊断为砂粒体性黑色素性神经鞘瘤。体格检查未发现卡尼综合征的体征。患者拒绝了手术切除肿物的建议。我们在此描述一例通过FNAB明确诊断为砂粒体性黑色素性神经鞘瘤的病例。