结论PPNAD是柯兴综合征的一种少见类型，诊断有赖于内分泌检查结果和病理学诊断，手术是治愈本病的有效方法。
Conclusion PPNAD is a rare type of Cushing syndrome. Diagnose depends on endocrine exams and pathological results. Operation is the effective method for the disease.
结果全部病例经手术治愈，病理诊断：肌间或灶性出血20例，机化血块10例，机化血栓9例。
Results All patients were healed by surgical operations, the pathological diagnosis revealed that among 39 patients, 20 with hemorrhage in muscles, 10 with fibrosis gore, 9 with fibrosis thrombus.
局灶型（占46.7%）仅表现为局部淋巴结肿大，病理形态学多表现为透明血管型，手术切除肿大淋巴结后治愈。
The unicentric CD(46.7%) just presented with local lymphadenopathy and was classified as the hyaline vascular type. The patients were cured by surgical resection of lymph node.
这一治疗方案能够防止HIV 病毒耐药株的产生，减少单一作用靶点药物的用药剂量和降低相应的毒性，最终治愈AIDS相关的病理学变化。
This approach could prevent the development of drug-resistant HIV strains and decrease the dosage and related toxicity of each single drug and lead to a cure for AIDS-associated pathologies.
方法回顾性分析经手术、穿刺活检病理检查证实或抗结核治疗治愈而确诊的7例脾结核的CT表现。
Methods CT features in 7 patients with STB proved by surgery or biopsy from 1998 to 2005 were retrospectively reviewed.
方法回顾性分析经手术、穿刺活检病理检查证实或抗结核治疗治愈而确诊的7例脾结核的CT表现。
Methods CT features in 7 patients with STB proved by surgery or biopsy from 1998 to 2005 were retrospectively reviewed.
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