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起源于良性神经鞘瘤并伴有多发脊柱骨内转移的梭形细胞型恶性外周神经鞘膜瘤:一例报告

Spindle cell type malignant peripheral nerve sheath tumor arising in benign schwannoma with multiple intraosseous spinal metastasis: A case report.

作者信息

Chung Jae Yoon, Kim Sung Sun, Kim Sung Kyu

机构信息

Department of Orthopedic Surgery, Chonnam National University Hospital, Gwangju, Korea.

Department of Pathology, Chonnam National University Hospital, Gwangju, Korea.

出版信息

J Back Musculoskelet Rehabil. 2017 Sep 22;30(5):1129-1135. doi: 10.3233/BMR-169590.

Abstract

BACKGROUND

Malignant peripheral nerve sheath tumor (MPNST) arising in benign schwannoma with multiple intraosseous spinal metastasis is extremely rare, having a highly aggressive progression and poor prognosis. In such cases, the malignant cells of MPNST usually have an epithelioid morphology. Here, the authors present a very rare case of spindle cell type MPNST arising in benign schwannoma.

CASE

A 47-year-old woman had a history of wide marginal excision of right buttock spindle cell sarcoma previously. However, metastatic lesions to C7, L1 body, and the right lung were detected during follow-up. Total spondylectomy and stabilization of the C7 and L1 tumors were performed within an interval of 5 months. However, the patient expired 6 months after the last surgery. From analysis and study of three tumor specimens (right buttock, cervical and lumbar spine), the pathological diagnosis based on histomorphologic and immunohistochemical studies was spindle cell sarcoma, high grade, most consistent with MPNST arising in schwannoma.

RESULTS

It is important that pathologists and surgeons recognize that spindle cell type MPNST may arise in benign schwannoma, as this recognition aids in assessment of patients with schwannoma and contributes to the pathologist making a more precise diagnosis, and the surgeon better determining the appropriate therapeutic options and surgical methods.

摘要

背景

起源于良性神经鞘瘤并伴有多发脊柱骨内转移的恶性外周神经鞘膜瘤(MPNST)极为罕见,具有高度侵袭性进展且预后不良。在这类病例中,MPNST的恶性细胞通常具有上皮样形态。在此,作者报告一例起源于良性神经鞘瘤的极为罕见的梭形细胞型MPNST病例。

病例

一名47岁女性既往有右臀部梭形细胞肉瘤广泛边缘切除史。然而,随访期间发现C7、L1椎体及右肺有转移灶。在5个月内对C7和L1肿瘤进行了全脊椎切除术及固定术。但患者在最后一次手术后6个月死亡。通过对三个肿瘤标本(右臀部、颈椎和腰椎)的分析研究,基于组织形态学和免疫组化研究的病理诊断为高级别梭形细胞肉瘤,最符合起源于神经鞘瘤的MPNST。

结果

病理学家和外科医生认识到梭形细胞型MPNST可能起源于良性神经鞘瘤很重要,因为这种认识有助于评估神经鞘瘤患者,有助于病理学家做出更精确的诊断,也有助于外科医生更好地确定合适的治疗方案和手术方法。

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