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例1:男,51岁。一月前开始头痛,渐出现智力低下,反应迟钝。于1986年5月29日入院。入院时神志清,反应迟钝。全身浅表淋巴结不大。视觉正常,双侧视乳头水肿。心、肺、腹检查无异常发现。克氏征及巴氏征阴性。四肢肌力及腱反射正常。血常规正常,血沉25mm/h。头颅CT示右颞顶占位性病变。临床诊断为脑膜瘤。于同年6月20日行颅脑手术,术中于颞顶深约1.5cm处可见粉红色瘤体,质脆,边界清,约3×3×4cm大小。完整切除肿瘤。病理诊断:非何杰金氏淋巴瘤,(氵弥)散性大小细胞混合型,中
Example 1: Male, 51 years old. A month ago began a headache, gradually appear mental retardation, unresponsive. May 29, 1986 admission. Conscious when admitted, unresponsive. Systemic superficial lymph nodes is not large. Visual acuity, bilateral papilledema. Heart, lung, abdominal examination no abnormal findings. Kirschner sign and Pakistan sign negative. Limb muscle strength and tendon reflexes normal. Normal blood, erythrocyte sedimentation rate 25mm / h. Head CT showed right temporal top occupying lesions. Clinical diagnosis of meningioma. In June 20 the same year, craniocerebral surgery, intraoperative at the top of the pit at a depth of about 1.5cm visible pink tumor, crisp, clear boundary, about 3 × 3 × 4cm size. Complete removal of the tumor. Pathological diagnosis: non-Hodgkin’s lymphoma, (Mi Mi) diffuse size cell mixed type, medium