结果：肾上腺皮质腺瘤45例，肾上腺皮质增生1例。
Results: Of which, 45 cases were adrenal adenomas and 1 adrenocortical hyperplasia.
结合临床资料，肾上腺皮质腺瘤能与部分肾上腺病变鉴别。
Combined with clinic date, adrenocortical adenoma can be differentiated from other adrenal diseases.
显微镜下，右侧的肾上腺皮质腺瘤类似正常的肾上腺束状带，左边为包膜。肿瘤细胞具有一定的异型性。
Microscopically, the adrenal cortical adenoma at the right resembles normal adrenal fasciculata. The capsule is at the left. There may be some cellular pleomorphism.
结果皮质腺瘤12例，皮质腺癌5例，嗜铬细胞瘤3例，髓样脂肪瘤4例，转移瘤6例，肾上腺节细胞神经瘤1例。
Results Of 31 cases, there were 12 adenomas, 5 adenocarcinomas, 3 pheochromocytomas, 4 myelolipomas, 6 metastatic tumor and 1 adrenal ganglioneuroma.
结果：本组99例肾上腺肿瘤中，腺瘤32例，嗜铬细胞瘤41例，髓性脂肪瘤5例，皮质腺癌8例，转移瘤13例。
Results: Of 99 adrenal tumors, 32 cases were adenoma, 41 cases were pheochromocytoma, 5 cases were adrenal myelolipoma, 8 cases were adenocarcinoma and 13 cases were metastatic tumors.
皮质醇腺瘤肿块稍大，中等密度。
术后病理检查证实：原发性醛固酮增多症8例，皮质醇腺瘤2例，嗜铬细胞瘤2例。
The pathologic study confirm that 8 cases were primary aldosteronism, 2 cases adrenocortical adenoma, 2 cases pheochromocytoma.
目的探讨儿童和青春期垂体促肾上腺皮质激素(ACTH)微腺瘤的诊断和治疗方法。
Objective To investigate the methods of diagnosis and treatment of pediatric and hebetic adrenocorticotropic hormone (ACTH) secreting pituitary microadenoma.
结果4 5例中醛固酮瘤15例，误诊的双侧肾上腺增生3例，嗜铬细胞瘤8例，腺瘤、腺癌型皮质醇增多症4例和意外瘤15例。
Results Of 45 cases, 15 were with aldosterone producing adenoma (APA), 3 with of BAH, 8 pheochromocytoma, 4 adrenal tumor with hypercortisolism and 15 adrenal incidentaloma.
下边是皮质增生的肾上腺，可能是垂体腺瘤分泌acth (Cushing病)，或异位分泌acth引起的库欣综合征，或特发性肾上腺增生。
This could be due to a pituitary adenoma secreting ACTH (Cushing's disease), or Cushing's syndrome from ectopic ACTH production, or idiopathic adrenal hyperplasia.
下边是皮质增生的肾上腺，可能是垂体腺瘤分泌acth (Cushing病)，或异位分泌acth引起的库欣综合征，或特发性肾上腺增生。
This could be due to a pituitary adenoma secreting ACTH (Cushing's disease), or Cushing's syndrome from ectopic ACTH production, or idiopathic adrenal hyperplasia.
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