产生醛固酮的肾上腺皮质癌具有不寻常的初始表现:一个罕见的疾病和病例报告

Jen-Hwa Chen, T. Wei, C. Pan, Yen-Hua Chang, William V. Huang
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引用次数: 0

摘要

醛固酮产生性肾上腺皮质癌(APAC)极为罕见。它不仅是最罕见的功能性肾上腺皮质癌(ACC),也是原发性醛固酮增多症(PH)最罕见的病因。此外,如果ACC患者出现高血压和低钾血症,则更有可能继发于糖皮质激素的过量产生,而不是ph。据我们所知,台湾尚未报道APAC有详细的临床表现。我们报告了一位由于不寻常的初始表现而被诊断为APAC的患者,主要是右侧精索静脉曲张,通过整体切除成功治疗,无病10个月。由于APAC的罕见性和不良预后,我们报告患者的临床病程、治疗和随访结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aldosterone-producing adrenocortical carcinoma with unusual initial presentations: A rare disease and case report
Aldosterone-producing adrenocortical carcinoma (APAC) is extremely rare. It is not only the rarest functional adrenocortical carcinoma (ACC) but also the most infrequent cause of primary hyperaldosteronism (PH). Furthermore, if hypertension and hypokalemia present in a patient with ACC, they are more likely secondary to overproduction of glucocorticoid, rather than PH. To our knowledge, APAC has not yet been reported in Taiwan with detailed clinical manifestations. We present a patient diagnosed with APAC due to an unusual initial presentation, predominantly right-sided varicocele, treated successfully by en bloc resection, being disease-free for 10 months. Due to the rarity and unfavorable outcomes of APAC, we report the patient's clinical course, treatment, and follow-up outcomes.
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来源期刊
自引率
0.00%
发文量
16
审稿时长
24 weeks
期刊介绍: JCRP aims to provide an exchange forum for the cancer researchers and practitioners to publish their timely findings in oncologic disciplines. The scope of the Journal covers basic, translational and clinical research, Cancer Biology, Cancer Immunotherapy, Hemato-oncology, Digestive cancer, Urinary tumor, Germ cell tumor, Breast cancer, Lung cancer, Head and Neck Cancer in a vast range of cancer related topics. The Journal also seeks to enhance and advance the cancer care standards in order to provide cancer patients the best care during the treatments.
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