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骶部脊髓脉络丛癌初次发病17年后的延迟复发

Delayed Recurrence of Choroid Plexus Carcinoma in the Sacral Spinal Cord 17 Years after Its Initial Presentation.

作者信息

Nagai Arata, Kanamori Masayuki, Shimoda Yoshiteru, Watanabe Mika, Saito Ryuta, Kumabe Toshihiro, Aizawa Toshimi, Tominaga Teiji

机构信息

Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.

Department of Pathology, Tohoku University Hospital, Sendai, Miyagi, Japan.

出版信息

NMC Case Rep J. 2022 Sep 15;9:301-306. doi: 10.2176/jns-nmc.2022-0056. eCollection 2022.

Abstract

Choroid plexus carcinomas (CPCs) are rare malignant tumors of neuro-ectodermal origin, accounting for less than 1% of all intracranial tumors. The recurrence rates of CPCs are very high and typically occur in the short-term following surgery, even after gross total removal. Here we present a rare case of CPC with spinal metastasis, which occurred long after its initial presentation. A 25-year-old woman with a history of increased intracranial pressure underwent resection for a tumor of the fourth ventricle, with a histopathological diagnosis of CPC. After tumor resection, she received 30 Gy of radiation therapy to the craniospinal axis and 20 Gy to the primary site, followed by nimustine hydrochloride chemotherapy. The residual lesion completely responded to these treatments. She suffered sensory loss in the sacral region 13 years later, followed by refractory skin ulcer in the sacral region 17 years after the initial treatments. Magnetic resonance imaging at 17 years after the initial treatments showed tumor in the sacral region, which was enlarged upon follow-up after 18 months, causing incontinence and loss of urinary intention. She underwent tumor resection, with a histological diagnosis of recurrent CPC. She received salvage re-irradiation. This case shows that CPC can spread via the cerebrospinal fluid pathways and cause spinal metastasis, with relatively slow clinical course. The present case suggests that patients with CPCs may need long-term follow-up imaging of the total neural axis to identify late recurrence at both the primary site and spinal metastasis.

摘要

脉络丛癌(CPCs)是一种罕见的神经外胚层起源的恶性肿瘤,占所有颅内肿瘤的比例不到1%。CPCs的复发率非常高,通常在手术后短期内发生,即使是在肿瘤全切之后。在此,我们报告一例罕见的CPC伴有脊柱转移的病例,其在初次发病很久之后才出现转移。一名有颅内压升高病史的25岁女性因第四脑室肿瘤接受了切除术,组织病理学诊断为CPC。肿瘤切除后,她接受了全脑脊髓轴30 Gy的放射治疗和原发部位20 Gy的放射治疗,随后进行了盐酸尼莫司汀化疗。残留病灶对这些治疗完全缓解。13年后,她出现骶部感觉丧失,初始治疗17年后,骶部出现难治性皮肤溃疡。初始治疗17年后的磁共振成像显示骶部有肿瘤,18个月后随访发现肿瘤增大,导致尿失禁和尿意丧失。她接受了肿瘤切除术,组织学诊断为复发性CPC。她接受了挽救性再放疗。该病例表明,CPC可通过脑脊液途径扩散并导致脊柱转移,临床病程相对缓慢。本病例提示,CPC患者可能需要对整个神经轴进行长期随访成像,以发现原发部位和脊柱转移的晚期复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8995/9534564/eb800ae2e039/2188-4226-9-0301-g001.jpg

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