[1例醛固酮产生性肾上腺皮质癌]。

Q4 Medicine
Hiroki Oshiro, Yousuke Shimizu, Ryota Nakayasu, Noriaki Utsunomiya, Cheol Son, Kazuo Tsuji, Satsuki Asai, Hiroki Katsushima, Misa Ishihara, Kimio Hashimoto, Sojun Kanamaru
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引用次数: 0

摘要

59岁男性,表现为高血压、低血钾和肌肉无力。醛固酮/肾素比值高,血浆肾素活性低。计算机断层扫描(CT)显示一个不均匀的左肾上腺肿块。确诊为原发性醛固酮增多症,行腹腔镜左肾上腺切除术。病理诊断为肾上腺皮质癌伴手术切缘阳性。他接受了放疗和米托坦作为辅助治疗。随后,CT显示肝脏和腹膜后多发转移灶。经6个疗程的EDP(依托泊苷、阿霉素和顺铂联合治疗)后,CT显示腹膜后广泛转移,患者选择接受最佳支持治疗。醛固酮产生的肾上腺皮质癌极为罕见。据我们所知,仅报告了67例。需要完全切除以改善预后,但我们的病例没有做到这一点。因此,我们建议谨慎选择手术程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A Case of Aldosterone-Producing Adrenocortical Carcinoma].

A 59-year-old man presented with high blood pressure, hypokalemia and muscle weakness. His aldosterone/renin ratio was high and plasma renin activity was low. Computed tomography (CT) showed a heterogeneous left adrenal mass. Primary aldosteronism was diagnosed and laparoscopic left adrenalectomy was performed. The pathological diagnosis was adrenocortical carcinoma with positive surgical margins. He underwent radiotherapy and mitotane as adjuvant therapies. Subsequently, CT revealed multiple metastases, in the liver and retroperitoneum. After six courses of EDP (a combination of etoposide, doxorubicin and cisplatin), CT showed widespread metastases in the retroperitoneum and he chose to receive the best supportive care. Aldosterone-producing adrenocortical carcinoma is exceedingly rare. To the best of our knowledge, only67 cases have been reported. Complete resection is needed to improve prognosis and this was not achieved in our case. We therefore recommend careful selection of the operative procedure.

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来源期刊
Acta Urologica Japonica
Acta Urologica Japonica Medicine-Medicine (all)
CiteScore
0.20
自引率
0.00%
发文量
74
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