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[一例伴有脑转移的腺泡状软组织肉瘤]

[A case of alveolar soft-part sarcoma with cerebral metastases].

作者信息

Haga Y, Kusaka G, Mori S, Shinoda S, Masuzawa T

机构信息

Department of Surgical Neurology, Jichi Medical School, Tochigi, Japan.

出版信息

No To Shinkei. 1996 Mar;48(3):269-74.

PMID:8868339
Abstract

A case of alveolar soft-part sarcoma with multiple cerebral metastases in addition to multiple lung and bone metastases is reported. This is a rare tumor which thus far has only been recognized as a malignant soft tissue tumor with great uncertainty. A 24-year-old man with a chief complaint of left frontal headache was admitted to our unit on September 26, 1994. A tumor of the right forearm had been surgically removed 9 years previously, and surgery had been followed by two courses of chemotherapy with vincristine, cyclophosphamide and actinomycin-D and subsequent irradiation for bone metastasis. The chemotherapy, however, did not have any clear effect. Neurological examination at the time revealed only bilateral papilledema, but CT and MRI scan of the brain showed a round mass in the left occipital lobe with homogeneous enhancement and another small mass was detected in the right occipital lobe. A cerebral angiogram showed a vascular tumor. The preoperative diagnosis was multiple cerebral metastases of alveolar soft part sarcoma. Left occipital craniotomy was performed on October 12, 1994, and the tumor was completely removed by lobectomy. Specimens of the tumor showed typical histological features of alveolar soft-part sarcoma. Whole-brain radiotherapy was administered postoperatively, and the patient is well neurologically without right homonymous hemianopsia. The clinical features of alveolar soft-part sarcoma are discussed. Only a few cases have been reported in the literature, but the most frequent site of the primary lesion has been the lower extremities, and cerebral metastasis has not been rare. All efforts should be focused on discovering this tumor in the early stage because surgical removal can yield good results, and radiotherapy is thought to be effective in terms of patient "quality of life".

摘要

报告了一例肺泡软部肉瘤,除多发肺和骨转移外,还伴有多发脑转移。这是一种罕见的肿瘤,迄今为止仅被认为是一种恶性软组织肿瘤,存在很大的不确定性。一名24岁男性,主要症状为左前额头痛,于1994年9月26日入住我院。9年前曾手术切除右前臂肿瘤,术后接受了两疗程长春新碱、环磷酰胺和放线菌素-D化疗,随后对骨转移进行了放疗。然而,化疗没有明显效果。当时的神经学检查仅发现双侧视乳头水肿,但脑部CT和MRI扫描显示左枕叶有一个圆形肿块,强化均匀,右枕叶还发现另一个小肿块。脑血管造影显示为血管性肿瘤。术前诊断为肺泡软部肉瘤多发脑转移。1994年10月12日进行了左枕部开颅手术,通过肺叶切除术将肿瘤完全切除。肿瘤标本显示出肺泡软部肉瘤典型的组织学特征。术后进行了全脑放疗,患者神经功能良好,无右侧同向性偏盲。讨论了肺泡软部肉瘤的临床特征。文献中仅报道了少数病例,但原发灶最常见的部位是下肢,脑转移并不罕见。应尽一切努力在早期发现这种肿瘤,因为手术切除可取得良好效果,并且就患者“生活质量”而言,放疗被认为是有效的。

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