具有全身转移的胶质瘤对异环磷酰胺、卡铂和依托泊苷化疗反应良好:一个尸检病例报告。

NMC Case Report Journal Pub Date : 2022-08-26 eCollection Date: 2022-01-01 DOI:10.2176/jns-nmc.2022-0075
Yuki Nakagaki, Keitaro Kai, Yoshihiro Komohara, Tatsuya Takezaki, Junichiro Kuroda, Naoki Shinojima, Mari Shimomura, Fumi Kawakami, Yoshiki Mikami, Akitake Mukasa
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摘要

胶质瘤是一种罕见的恶性肿瘤。它约占所有胶质母细胞瘤的2%。迄今为止,对于胶质肉瘤还没有确定的治疗方法,通常采用多种治疗方法,如手术切除、放疗和化疗。在这里,我们描述了一个胶质肉瘤患者,尽管肿瘤在全身转移,包括肺和淋巴结,但由于局部照射和低剂量异环磷酰胺、卡铂和依托泊苷治疗的显着有效的化疗,他获得了相对较长的生存期。病人死后,我们进行了尸检,确认了原发和转移性肿瘤细胞的性质,这些肿瘤细胞已经扩散到病人全身。临床和系统组织学研究也提示从全身转移灶再转移到脑部的可能性。胶质瘤似乎具有与肉瘤相似的特征以及更高的全身转移风险。因此,对此类患者进行仔细的随访是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Gliosarcoma with Systemic Metastasis Showing Favorable Response to Ifosfamide, Carboplatin, and Etoposide Chemotherapy: An Autopsy Case Report.

Gliosarcoma is a rare malignant neoplasm. It accounts for approximately 2% of all glioblastomas. To date, there is no established treatment method for gliosarcoma, and a variety of therapies, such as surgical resection, radiotherapy, and chemotherapy, are typically employed. Here, we describe a patient with gliosarcoma who, despite multiple tumor metastases throughout the body, including the lungs and lymph nodes, achieved a relatively long survival due to salvage therapy with local irradiation and remarkably effective chemotherapy with low-dose ifosfamide, carboplatin, and etoposide therapy. When the patient died, we performed autopsy and confirmed the nature of the primary and metastatic tumor cells that had spread throughout the patient's body. Clinical and systemic histological studies also suggested the possibility of re-metastasis to the brain from systemic metastatic foci. Gliosarcoma appears to have characteristics similar to sarcoma as well as a higher risk of systemic metastasis. Therefore, a careful follow-up is necessary in such patients.

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