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抗N-甲基-D-天冬氨酸受体脑炎治疗后的卵巢畸胎瘤发育

Ovarian teratoma development after anti-NMDA receptor encephalitis treatment.

作者信息

Omata Taku, Kodama Kazuo, Watanabe Yoshimi, Iida Yukiko, Furusawa Yoshiaki, Takashima Akiko, Takahashi Yukitoshi, Sakuma Hiroshi, Tanaka Keiko, Fujii Katsunori, Shimojo Naoki

机构信息

Division of Child Neurology, Chiba Children's Hospital, Chiba, Japan.

Division of Child Neurology, Chiba Children's Hospital, Chiba, Japan.

出版信息

Brain Dev. 2017 May;39(5):448-451. doi: 10.1016/j.braindev.2016.12.003. Epub 2016 Dec 28.

Abstract

BACKGROUND

Anti-NMDA-R receptor encephalitis occurs predominantly in younger women and is often comorbid with ovarian teratoma, a feature that is often absent in children. Here, we report our experience with two pediatric patients, in whom no tumors were present during treatment for encephalitis, but in whom ovarian teratomas developed without encephalitis relapse after treatment was completed.

CASES

Patient 1 was a 14-year-old girl who was diagnosed due to characteristic symptoms and anti-NMDA-R antibody. MRI scanning during treatment revealed no ovarian tumors, but a tumor developed in the right ovary 10months after onset. Another tumor developed in the left ovary 3years after onset, and a mature ovarian teratoma was confirmed after bilateral partial ovariectomy. Patient 2 was an 11-year old girl who was also diagnosed due to characteristic symptoms and anti-NMDA-R antibody. Imaging during treatment revealed no ovarian tumors, but a 2.5-cm tumor mass was found in the left ovary 10months after onset, and a mature ovarian teratoma was confirmed after partial ovariectomy.

DISCUSSION

This case report suggests the need for regular tumor screening after treatment for anti-NMDA receptor encephalitis because of potential subsequent tumor development, even in pediatric patients who initially present with no comorbid tumors. No analysis of relapse risk has yet been reported in cases of tumor development after treatment, and at this point, whether or not resection is needed to prevent relapse remains unclear. However, because teratomas usually grow, have an associated risk of torsion, and can be malignant, tumor removal should be considered.

摘要

背景

抗N-甲基-D-天冬氨酸受体(NMDA-R)脑炎主要发生于年轻女性,常与卵巢畸胎瘤合并存在,而这一特征在儿童中往往不存在。在此,我们报告两例儿科患者的情况,这两名患者在脑炎治疗期间未发现肿瘤,但在治疗结束后出现了卵巢畸胎瘤,且脑炎未复发。

病例

患者1是一名14岁女孩,因典型症状和抗NMDA-R抗体而被确诊。治疗期间的MRI扫描未发现卵巢肿瘤,但发病10个月后右侧卵巢出现一个肿瘤。发病3年后左侧卵巢又出现一个肿瘤,双侧部分卵巢切除术后确诊为成熟性卵巢畸胎瘤。患者2是一名11岁女孩,同样因典型症状和抗NMDA-R抗体而被确诊。治疗期间的影像学检查未发现卵巢肿瘤,但发病10个月后左侧卵巢发现一个2.5厘米的肿瘤肿块,部分卵巢切除术后确诊为成熟性卵巢畸胎瘤。

讨论

本病例报告表明,抗NMDA受体脑炎治疗后需要定期进行肿瘤筛查,因为即使是最初未合并肿瘤的儿科患者,后续也可能发生肿瘤。目前尚无关于治疗后出现肿瘤病例的复发风险分析报告,此时是否需要切除肿瘤以预防复发尚不清楚。然而,由于畸胎瘤通常会生长,有扭转风险,且可能恶变,因此应考虑切除肿瘤。

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