Zingrillo M, Errico M, D'Aloiso L, Torlontano M, Parracino T, Gomes V
Istituto di Ricovero e Cura a Carattere Scientifico, Ospedale Casa Sollievo della Sofferenza, San Giovanni Rotondo (Foggia).
Minerva Endocrinol. 1991 Oct-Dec;16(4):193-7.
The Authors report a case of left adrenal mass incidentally discovered by upper abdominal echogram in a 40 year old man. Physical examination showed no signs of hypercortisolism and plasma cortisol and ACTH levels were in the normal range as well as urinary free cortisol. After adrenalectomy, 4 and 8 month follow-up was performed, without clinical, hormonal and TC evolution. Thirteen months later the patient was referred to our department for widespread oedema, hypertension, hypokalemia and alkalosis. These symptoms were associated with dramatically elevated concentrations of plasmatic and free urinary cortisol. TC showed a large mass in the same adrenal region and diffuse hepatic metastases. In spite of mitotane and ketoconazole therapy the patient died few weeks later.
作者报告了一例40岁男性患者,上腹部超声检查偶然发现左肾上腺肿块。体格检查未发现皮质醇增多症迹象,血浆皮质醇、促肾上腺皮质激素(ACTH)水平以及尿游离皮质醇均在正常范围内。肾上腺切除术后,进行了4个月和8个月的随访,临床、激素及计算机断层扫描(TC)均无进展。13个月后,该患者因全身水肿、高血压、低钾血症和碱中毒转诊至我科。这些症状与血浆和尿游离皮质醇浓度显著升高有关。TC显示同一肾上腺区域有一个大肿块及弥漫性肝转移。尽管使用了米托坦和酮康唑治疗,患者几周后仍死亡。