Meah F A, Abdullah T, Jasmi A Y, Hisham A N, Tan T T, Khalid B A, Tahir A
Department of Surgery, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Ann Acad Med Singap. 1996 Mar;25(2):251-4.
Between January 1978 to December 1993, 130 cases of adrenal diseases were diagnosed and surgically treated at the National University of Malaysia. They were 58 cases (44.6%) of Conn's syndrome, 40 cases (30.7%) of Cushing's syndrome, 20 cases (15.3%) of phaeochromocytoma and 12 cases (9.2%) of adrenocortical carcinoma (ACC). The commonest cause of Conn's syndrome was an adenoma (96.5%) which affected the left gland four times more than the right gland. Cushing's syndrome was caused by adrenocortical adenoma (32.5%), diffuse bilateral adrenal hyperplasia (40.0%), pigmented macronodular hyperplasia (20.0%) and adrenal carcinoma (7.5%). Twenty-five percent of the phaeochromocytomas were extraadrenal in origin arising mainly from the abdominal sympathetic chain. More than 50% of ACCs were non-functioning tumours. Fifty percent of the patients with ACC had inoperable tumours. The prognosis was poor even with adjuvant chemoradiotherapy. The main surgical approach was the anterior transabdominal route. There was no operative mortality or morbidity in all operated cases.
1978年1月至1993年12月期间,马来西亚国立大学诊断并手术治疗了130例肾上腺疾病。其中,原发性醛固酮增多症58例(44.6%),库欣综合征40例(30.7%),嗜铬细胞瘤20例(15.3%),肾上腺皮质癌(ACC)12例(9.2%)。原发性醛固酮增多症最常见的病因是腺瘤(96.5%),左侧肾上腺受累的几率是右侧的四倍。库欣综合征的病因包括肾上腺皮质腺瘤(32.5%)、双侧肾上腺弥漫性增生(40.0%)、色素沉着性大结节性增生(20.0%)和肾上腺癌(7.5%)。25%的嗜铬细胞瘤起源于肾上腺外,主要来自腹部交感神经链。超过50%的肾上腺皮质癌为无功能性肿瘤。50%的肾上腺皮质癌患者肿瘤无法切除。即使进行辅助放化疗,预后也很差。主要的手术方式是经腹前路。所有手术病例均无手术死亡或并发症。