Miyakoshi Naohisa, Nishikawa Yuji, Shimada Yoichi, Okada Kyoji, Yoshida Masayuki, Enomoto Katsuhiko, Itoi Eiji
Department of Orthopedic Surgery, Akita University School of Medicine, Akita 010-8543, Japan.
Neurol India. 2007 Jan-Mar;55(1):64-6. doi: 10.4103/0028-3886.30431.
The authors describe an extremely rare case with malignant peripheral nerve sheath tumor (MPNST) with focal epithelioid differentiation presenting as an intraosseous lesion of the spine. A 75-year-old woman presented with progressive paraplegia caused by epidural mass arising from the posterior element of the T7 vertebra. At surgery, the lesion was noted to originate from the T7 vertebra and separate from the dura and spinal nerve roots. The patient died of tumor metastases to the lungs six months after the initial presentation. Histological diagnosis was MPNST. However, the tumor also contained cystic structures lined by epithelioid cells, requiring differentiation from synovial sarcoma. From the histological and immunohistochemical features, as well as the absence of SYT-SSX fusion gene expression, the diagnosis of MPNST with focal epithelioid differentiation was made. This is the first case report of intraosseous MPNST of the spine with a peculiar biphasic appearance.
作者描述了一例极为罕见的病例,为伴有局灶性上皮样分化的恶性外周神经鞘瘤(MPNST),表现为脊柱的骨内病变。一名75岁女性因T7椎体后部硬膜外肿块导致进行性截瘫就诊。手术中发现病变起源于T7椎体,与硬脑膜和脊神经根分离。患者在初次就诊后6个月死于肿瘤肺转移。组织学诊断为MPNST。然而,肿瘤还包含由上皮样细胞衬里的囊性结构,需要与滑膜肉瘤相鉴别。根据组织学和免疫组化特征,以及SYT-SSX融合基因表达缺失,做出了伴有局灶性上皮样分化的MPNST的诊断。这是首例具有独特双相外观的脊柱骨内MPNST的病例报告。