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[平滑肌肉瘤转移至蝶骨导致眼球突出:一例报告]

[Leiomyosarcoma metastatizing to the sphenoid bone presenting exophthalmos: a case report].

作者信息

Matsumoto S, Yamamoto T, Ban S, Sato S, Yoshida S, Tokuno T, Nakazawa K, Uchida H

机构信息

Department of Neurosurgery, Kobe City General Hospital.

出版信息

No Shinkei Geka. 1995 Jul;23(7):621-5.

PMID:7637846
Abstract

A rare subcutaneous leiomyosarcoma metastatizing to the sphenoid bone and presenting exophthalmos is reported. A 56-year-old female presented with protrusion of the right eye and a slowly growing lump on the right temporal region. Six years previously, she had undergone removal of a subcutaneous mass in the back, which was histologically diagnosed in another hospital as leiomyosarcoma. She had undergone four other operations, including removal of local recurrences and a right renal metastasis. On admission, physical examination showed no neurological deficits. Craniogram revealed an osteolytic lesion without marginal sclerosis in the right sphenoid bone. CT showed an inhomogeneously enhanced mass with irregular expansion of the diploic space, which was partly invading the right orbit. MRI demonstrated an extradural mass in the right sphenoid region, which was slightly low-intense in T1-weighted image, high-intense in T2-weighted image, and inhomogeneously enhanced by Gd-DTPA. Right external carotid angiogram showed a highly vascular stain fed by meningeal arteries. Radionuclide bone scintigram showed multiple high-uptake areas in the left femoral head, the ribs, and the sphenoid bone. Preoperative embolization of the tumor vessels fed by the external carotid artery was performed. Following this procedure, the tumor stain disappeared completely. The tumor was totally excised with minimal bleeding through an orbitozygomatic approach. The tumor was loosely adherent to the dura and periorbit. The bone defect was covered with a methylmethacrylate resin plate. the histological examination demonstrated fascicular arrangement of the spindle shaped cells with mitotic figures. Immunohistochemical studies showed that most tumor cells were positive for actin and myosin, but negative for desmin.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报告了一例罕见的皮下平滑肌肉瘤转移至蝶骨并导致眼球突出的病例。一名56岁女性,右眼突出,右侧颞部有一缓慢生长的肿块。6年前,她曾接受背部皮下肿物切除术,在另一家医院经组织学诊断为平滑肌肉瘤。她还接受了另外4次手术,包括切除局部复发灶和右肾转移灶。入院时,体格检查未发现神经功能缺损。颅骨X线片显示右侧蝶骨有一溶骨性病变,无边缘硬化。CT显示一不均匀强化肿块,板障间隙不规则扩大,部分侵犯右侧眼眶。MRI显示右侧蝶骨区域硬膜外肿块,T1加权像呈稍低信号,T2加权像呈高信号,Gd-DTPA增强不均匀。右侧颈外动脉血管造影显示由脑膜动脉供血的高血运染色区。放射性核素骨扫描显示左侧股骨头、肋骨和蝶骨有多个高摄取区。对由颈外动脉供血的肿瘤血管进行了术前栓塞。栓塞后,肿瘤染色完全消失。通过眶颧入路以最小的出血量将肿瘤完整切除。肿瘤与硬脑膜和眶周组织疏松粘连。骨缺损用甲基丙烯酸甲酯树脂板覆盖。组织学检查显示梭形细胞呈束状排列并可见核分裂象。免疫组织化学研究显示,大多数肿瘤细胞肌动蛋白和肌球蛋白呈阳性,但结蛋白呈阴性。(摘要截短至250字)

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