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[一例颅底恶性淋巴瘤病例]

[A case of malignant lymphoma in the skull base].

作者信息

Tanaka S, Nihei H, Manaka S, Hori T

机构信息

Department of Neurosurgery, Ichihara Hospital, Teikyo University School of Medicine, Chiba, Japan.

出版信息

No Shinkei Geka. 1994 Jan;22(1):73-8.

PMID:8295707
Abstract

A case of malignant lymphoma located in the clivus, sella and cavernous sinus is reported. A 46-year-old female was hospitalized with a 3-week history of diplopia. Neurological examination showed left oculomotor, trochlear, abducens and hypoglossal nerve palsy. Improvement of cranial nerve palsy was achieved with the administration of prednisolone but it was only transient. Laboratory studies and endocrinological examination showed almost no abnormal findings. Skull x-ray film revealed a widely damaged base. MR studies showed a homogeneously enhanced mass lesion in the clivus, sella and bilateral cavernous sinus. Partial removal of the lesion was performed via the transsphenoidal route. The histopathological diagnosis of the mass was consistent with diffuse, medium sized cell, B-cell type malignant lymphoma. A postoperative systemic evaluation by tumor scan with 67Ga disclosed no abnormal uptake except in the skull base. Postoperatively, the patient was treated with radiation, a total of 50 Gy, followed by chemotherapy every 3 week consistent of cyclophosphamide, vincristine, pirarubicin, bleomycin, procarbazine and prednisolone. The cranial nerve symptoms disappeared during radiation therapy. The MR studies after three courses of chemotherapy revealed almost complete remission. The patient died of acute progression of pneumonia without any evidence of the recurrence of malignant lymphoma 10 months after the operation. Skull base involvement of malignant lymphoma is unusual. Five cases of malignant lymphoma invading the skull base have been reported since 1987. In most cases, the lesion originated from paranasal sinuses and was usually accompanied with intradural extensions. In the case we have reported there was no intradural invasion of the tumor.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报告一例位于斜坡、蝶鞍和海绵窦的恶性淋巴瘤。一名46岁女性因复视3周入院。神经学检查显示左侧动眼神经、滑车神经、展神经和舌下神经麻痹。给予泼尼松龙后颅神经麻痹有所改善,但只是暂时的。实验室检查和内分泌检查几乎未发现异常。颅骨X线片显示颅底广泛受损。磁共振成像(MR)研究显示斜坡、蝶鞍和双侧海绵窦有均匀强化的肿块病变。经蝶窦入路对病变进行了部分切除。肿块的组织病理学诊断与弥漫性、中等大小细胞、B细胞型恶性淋巴瘤一致。术后用67Ga肿瘤扫描进行全身评估,除颅底外未发现异常摄取。术后患者接受放疗,总量50 Gy,随后每3周进行一次化疗,化疗方案为环磷酰胺、长春新碱、吡柔比星、博来霉素、丙卡巴肼和泼尼松龙。放疗期间颅神经症状消失。三个疗程化疗后的MR研究显示几乎完全缓解。患者术后10个月死于肺炎急性进展,无恶性淋巴瘤复发迹象。恶性淋巴瘤累及颅底并不常见。自1987年以来已报告5例恶性淋巴瘤侵犯颅底。大多数情况下,病变起源于鼻窦,通常伴有硬膜内扩展。在我们报告的病例中,肿瘤没有硬膜内侵犯。(摘要截短至250字)

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