尽管如此，大部分的肾上腺瘤与遗传疾病无关。
However, most adrenal adenomas are not linked with an inherited disease.
过去要想切除肾上腺瘤必须从腹部、侧腹部或者背部开一个6至12英寸的切口。
In the past, making a large 6 to 12 inch incision in the abdomen, flank, or back was necessary for removal of an adrenal gland tumor.
大多数偶然发现的肾上腺肿块是不造成激素分泌异常的良性非功能性肾上腺瘤，没有任何症状，也不需要做切除。
Most incidentally found adrenal masses do not make excess hormones, cause no symptoms, are benign, and do not need to be removed.
偶然在肾上腺发现的肿块可能属于上述任何类型的功能性肾上腺瘤或者是不造成激素分泌异常的非功能性肾上腺瘤。
An incidentally found mass in the adrenal may be any of the above types of tumors, or may produce no hormones at all.
结论肾上腺瘤通过多层面螺旋CT三维重建后，可以更好地认识肾上腺，为更安全地施行后腹腔镜肾上腺切除术提供有力的帮助。
Conclusion adrenal tumors having been taken MSCT and 3-dimensional reconstruction, helping us to know the adrenal tumors better, provided good help for retroperitoneal laparoscopic adrenalectomy.
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.
高血压病人左侧肾上腺的直径为1.3厘米的腺瘤。
Here is a 1.3 cm left adrenal adenoma found in a patient with hypertension.
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.
目的探讨磁共振成像（MRI）对肾上腺腺瘤及增生的诊断价值。
Purpose To evaluate the adrenal neoplasms and cortical hyperplasia with MRI.
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.
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.
目的分析肾上腺大腺瘤的CT征象，对比大、小腺瘤的病理特征，提高对肾上腺大腺瘤的认识。
Objective to analyze the ct features of large adrenal adenoma and to compare the pathological features of large adenoma and small adenoma in order to improve the diagnosis of large adenoma.
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.
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.
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.
应用推荐