分泌性acth腮腺腺泡细胞癌是一种罕见的副肿瘤综合征。

Q3 Medicine Endocrine regulations Pub Date : 2022-07-13 DOI:10.2478/enr-2022-0017
Magdelene Doris Amoateng, Georges El Hasbani, Armando Vera, Jose Vargas, Abraham Rodriguez, Renu Cheriyan, Imran Siddiqui, Ilja Hulinsky
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引用次数: 0

摘要

由免疫交叉反应或激素/肽分泌引起的副肿瘤综合征是肿瘤的一种非典型表现。有些肿瘤,如小细胞肺癌和支气管类癌,可以是促肾上腺皮质激素(ACTH)分泌的肿瘤。不太常见的腮腺腺泡细胞癌可能是导致库欣综合征的acth分泌肿瘤。关于腮腺癌ACTH相关副肿瘤综合征的文献报道较少。由于这种情况罕见,对这种现象的治疗和预后知之甚少。在本报告中,我们报告了一位59岁男性患者,既往有腮腺癌病史,曾接受手术、化疗和放疗,临床和生化指标均表现为高醛固酮增多症。腹部超音波、电脑断层及核磁共振显示肝脏肿块。肝活检与免疫组织化学证实腮腺腺癌的存在分泌ACTH。他正在接受紫杉醇和卡铂药物治疗,临床反应良好。
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ACTH-secreting parotid acinic cell carcinoma unusually reported as a paraneoplastic syndrome.

Paraneoplastic syndromes, induced by an immunological cross-reaction or hormone/peptide secretion, are an atypical presentation of tumors. Some tumors, such as small cell lung cancer and bronchial carcinoid, can be adrenocorticotropic hormone (ACTH) secreting tumors. Less commonly, parotid acinic cell carcinoma can be ACTH-secreting tumor leading to Cushing's syndrome. Few literature cases have described ACTH related paraneoplastic syndrome of parotid adenocarcinoma. Because of the rarity of the condition, little is known about the management and prognosis of this phenomenon. In this report, we highlighted the case of a 59-year-old male with a past medical history of parotid adenocarcinoma treated with surgery, chemotherapy, and radiation therapy presented with clinical and biochemical signs of hyperaldosteronism. Abdominal ultra-sound, computed tomography, and magnetic resonance imaging showed hepatic mass. Liver biopsy with immunohistochemistry confirmed the presence of parotid adenocarcinoma secreting ACTH. He is on paclitaxel and carboplatin medication with good clinical response.

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来源期刊
Endocrine regulations
Endocrine regulations Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.70
自引率
0.00%
发文量
33
审稿时长
8 weeks
期刊最新文献
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