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经活检证实的延髓原发性中枢神经系统淋巴瘤,表现为厌食。

Biopsy-proven Primary CNS Lymphoma in the Medulla Oblongata Presenting as Anorexia.

作者信息

Kawajiri Takaharu, Takeuchi Hayato, Takahashi Yoshinobu, Shimura Yuji, Kuroda Junya, Hashimoto Naoya

机构信息

Department of Neurosurgery, Kyoto Prefectural University Graduate School of Medical Science, Kyoto, Kyoto, Japan.

Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University Graduate School of Medical Science, Kyoto, Kyoto, Japan.

出版信息

NMC Case Rep J. 2023 May 17;10:131-137. doi: 10.2176/jns-nmc.2022-0399. eCollection 2023.

Abstract

Eating disorders caused by brain tumors are infrequently seen. Recent studies revealed that a neurocircuit from the nucleus tractus solitarius of the medulla oblongata to the hypothalamus participates in the control of appetite. Among brain tumors, those located in the brain stem, especially a solitary one in the medulla oblongata, are rare. Tumors in the brainstem are generally considered gliomas, and with the difficulty in reaching the lesion, treatment without histological confirmation is often performed. However, there are a few reported cases of medulla oblongata tumors other than gliomas. We describe a case of a 56-year-old man who presented with persistent anorexia. Magnetic resonance images revealed a solitary tumor in the medulla oblongata. After several examinations, craniotomy for the biopsy of the tumor using the cerebellomedullary fissure approach was carried out and primary central nervous system lymphoma (PCNSL) was histologically proven. The patient was treated with effective adjuvant therapy and was discharged home after he recovered from the symptoms. No tumor recurrence was recognized 24 months after surgery. A PCNSL arising only from the medulla oblongata is very rare, and anorexia can be an initial symptom of a tumor in the medulla oblongata. Surgical intervention is safely achieved and is a key to a better clinical outcome.

摘要

脑肿瘤引起的饮食失调较为罕见。最近的研究表明,从延髓孤束核到下丘脑的神经回路参与食欲控制。在脑肿瘤中,位于脑干的肿瘤,尤其是延髓的孤立性肿瘤很罕见。脑干肿瘤通常被认为是胶质瘤,由于难以到达病变部位,常进行未经组织学证实的治疗。然而,有少数关于非胶质瘤的延髓肿瘤的报道病例。我们描述了一例56岁男性患者,其表现为持续性厌食。磁共振成像显示延髓有一个孤立性肿瘤。经过多项检查后,采用小脑延髓裂入路对肿瘤进行活检的开颅手术,组织学证实为原发性中枢神经系统淋巴瘤(PCNSL)。患者接受了有效的辅助治疗,症状缓解后出院。术后24个月未发现肿瘤复发。仅起源于延髓的PCNSL非常罕见,厌食可能是延髓肿瘤的首发症状。手术干预能够安全实施,是获得更好临床结果的关键。

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