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颅内腺泡状软组织肉瘤十分少见,主要为继发性,国内外文献中均很少报道。从1975年9月～1990年12月,我们遇到2例,占同期收治的1419例颅内肿瘤的 0.14％。现报告如下,并结合文献对其临床和病理特点加以讨论。 例1 女,31岁,因头痛、恶心、呕吐进行性加重半年于1977年9月9日入院。入院前5年曾手术切除右臀部腺泡状软组织肉瘤。检查:神志清,不语,双眼向右侧凝视,双侧视乳头水肿,左侧轻度中枢性面瘫,双侧锥体束征阳性。颅骨X线平片见脑回压迹增多。右颈动脉脑血管造影,正位示大脑前动脉明显向对侧孤形移位,
Intracranial acinar soft tissue sarcoma is very rare, mainly secondary, rarely reported in the literature at home and abroad. From September 1975 to December 1990, we encountered two cases, accounting for 0.14% of 1419 cases of intracranial tumors treated in the same period. Now report as follows, combined with the literature on its clinical and pathological features to be discussed. Example 1 Female, 31 years old, due to headache, nausea, vomiting, exacerbations Six months in September 9, 1977 admission. 5 years before admission had surgery to remove the right gluteal soft tissue sarcoma. Check: Consciousness, no words, his eyes staring to the right, bilateral papilla edema, left mild central paralysis, bilateral pyramidal tract signs positive. Skull X-ray film to see the brain back track increased. Right carotid artery angiography, anterior cerebral artery anterior was significantly displaced to the opposite side of the solitary,