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皮肤脑膜瘤罕见,国内报告尚少.本文报告两例,并略加讨论.例1.女性,67岁,住院号2563.枕部肿块逐渐增大半年,近因伴头痛就诊.无呕吐.检查:枕部见一肿块突出,约6×4×3厘米,质软.x线见肿块基部颅骨有骨质破坏.临床拟诊头皮粉瘤恶变.1978年5月16日于局麻下手术.术中见肿块表面包膜完整,血管丰富,基部与帽状腱膜粘连,深达颅骨,分离困难,未能完整切除.术中出血较多.术后情况尚好,但仍有头痛症状.出院后失访.
Skin meningioma is rare, the domestic report is still small.This article reports two cases, and a little discussion.Example 1. Female, 67 years old, hospital number 2563. Occipital tumor gradually increased six months, near due to headache treatment .No vomiting .Check : Occipital see a mass prominent, about 6 × 4 × 3 cm, soft .x line to see the base mass of the skull bone destruction .Clinical clinical diagnosis of scleroderma malignant transformation. May 16, 1978 under local anesthesia surgery. Surgery, see the surface of the tumor mass capsule complete, rich in blood vessels, the base and the aponeurosis adhesions, deep skull, separation difficulties, failed to complete resection .Hemorrhage more .Postoperative condition is good, but there are still headache symptoms. After losing the visit.