Kido Y, Kuwano H, Yano K, Mori M, Kitamura K
Department of Surgery II, Kyushu University, Fukuoka, Japan.
Tumori. 1992 Feb 29;78(1):59-62. doi: 10.1177/030089169207800115.
A 20-year-old man was admitted to Kyushu University Hospital with complaints of severe headache and episodic hypertension (200/100 mmHg). Ultrasonograms and computed tomographs revealed tumors in the left adrenal region and in the right lower lobe of the thyroid gland. Total thyroidectomy and left adrenalectomy were performed. The excised thyroid tumor and adrenal tumor were pathologically diagnosed as papillary adenocarcinoma and pheochromocytoma, respectively. A chromosome analysis revealed no karyotypic abnormality. Whereas the world literature records such occurrences in women, this is the first report of a simultaneous occurrence of pheochromocytoma and papillary adenocarcinoma of the thyroid in a young man.
一名20岁男性因严重头痛和发作性高血压(200/100 mmHg)入住九州大学医院。超声检查和计算机断层扫描显示左肾上腺区域和甲状腺右叶有肿瘤。进行了甲状腺全切术和左肾上腺切除术。切除的甲状腺肿瘤和肾上腺肿瘤经病理诊断分别为乳头状腺癌和嗜铬细胞瘤。染色体分析未发现核型异常。虽然世界文献记载了女性有此类病例,但这是首次报道一名年轻男性同时发生甲状腺乳头状腺癌和嗜铬细胞瘤。