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报告一例具有不同寻常临床表现和病理表现的巨细胞室管膜瘤。

Report of a case of giant cell ependymoma with unusual clinical and pathological presentation.

机构信息

Pathology Department, Hospital Pirovano, Buenos Aires, Argentina.

Plastic Surgery Unit, Hospital Pirovano, Buenos Aires, Argentina.

出版信息

Neuropathology. 2019 Aug;39(4):313-318. doi: 10.1111/neup.12580. Epub 2019 Jun 26.

Abstract

Giant cell ependymoma (GCE) is a very uncommon variant of ependymoma, known for having varying degrees of nuclear pleomorphism. There are only 34 reported cases of GCE in the English literature. We describe an additional case of a young woman who presented with a tumor located in sacral soft tissue, which was not connected to the spinal cord and did not show additional lesions in the central nervous system. Complete tumor resection was performed and no recurrences or metastasis were detected after 5 months of follow-up. Only one of all the reported GCE was located in the sacral subcutaneous region, where ependymomas are rarely found and usually have myxopapillary histology. Ours is the second report showing microscopic features of GCE in the soft-tissue region. GCE should be considered in the differential diagnosis of lumbosacral subcutaneous tumors to avoid misdiagnosing it as a malignant lesion. Since GCE could be an extraspinal extension of an intraneural ependymoma, it would be important to evaluate whether it is connected to the spinal cord.

摘要

巨细胞室管膜瘤(GCE)是一种非常罕见的室管膜瘤变体,以不同程度的核多形性为特征。在英文文献中仅报道了 34 例 GCE。我们描述了另一个年轻女性的病例,其肿瘤位于骶部软组织,与脊髓无连接,且中枢神经系统无其他病变。进行了完全肿瘤切除,随访 5 个月后未发现复发或转移。所有报道的 GCE 中只有 1 例位于骶骨皮下区域,而此处很少发现室管膜瘤,且通常具有黏液乳头型组织学特征。我们的报告是第二个显示软组织区域 GCE 微观特征的报告。在鉴别腰骶部皮下肿瘤时,应考虑 GCE,以避免误诊为恶性病变。由于 GCE 可能是神经内室管膜瘤的椎管外延伸,因此评估其与脊髓的连接情况非常重要。

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