Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Department of Pathology, Unit 85, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX, 77030, USA.
Head Neck Pathol. 2020 Jun;14(2):562-569. doi: 10.1007/s12105-019-01054-w. Epub 2019 Jul 30.
We report a rare case of Cushing's syndrome in a 59-year-old man who initially presented with concurrent acinic cell carcinoma of the parotid with high-grade transformation and co-existing papillary and medullary thyroid carcinomas, without noticeable cushinoid symptoms. Six-months later, he developed clinical features of Cushing's syndrome which coincided with disease progression in the form of lung metastasis and mediastinal lymphadenopathy. Ectopic adrenocorticotropic hormone (ACTH) production and protein expression was limited to the high-grade transformed component of acinic cell carcinoma and in the lymph node metastasis, and was absent in the conventional acinic cell carcinoma as well as in the papillary and medullary thyroid carcinoma. He received adjuvant chemotherapy and supportive management with interval improvement for 8 months followed by disease progression with increasing serum cortisol levels and bone metastasis. He was offered palliative chemotherapy, however, declined further therapy and was lost to follow up. We discussed clinical and pathologic implications of ectopic ACTH production associated with acinic carcinoma and also reviewed the literature of this rare paraneoplastic syndrome.
我们报告了一例罕见的库欣综合征病例,患者为 59 岁男性,最初表现为同时发生的腮腺涎腺闰管细胞癌伴高级别转化,以及共存的甲状腺乳头癌和髓样癌,但无明显库欣样症状。6 个月后,他出现了库欣综合征的临床特征,同时伴有肺转移和纵隔淋巴结病的疾病进展。异位促肾上腺皮质激素 (ACTH) 的产生和蛋白表达仅限于涎腺闰管细胞癌的高级别转化部分以及淋巴结转移,而在常规涎腺闰管细胞癌以及甲状腺乳头癌和髓样癌中均不存在。他接受了辅助化疗和支持性治疗,间隔 8 个月后病情有所改善,随后疾病进展,血清皮质醇水平升高并发生骨转移。他接受了姑息性化疗,但拒绝进一步治疗,并失访。我们讨论了与涎腺闰管细胞癌相关的异位 ACTH 产生的临床和病理意义,并回顾了这种罕见副肿瘤综合征的文献。