Gosain A K, Clark O H
Arch Surg. 1984 May;119(5):515-9. doi: 10.1001/archsurg.1984.01390170015004.
We studied the records of patients with Hürthle cell neoplasms seen at the University of California at San Francisco, from 1943 to 1982, because of controversy concerning the malignant potential of these tumors. Of our 84 patients, 71 had Hürthle cell adenomas (HCAs), nine had Hürthle cell change in chronic thyroiditis, and four had Hürthle cell carcinomas. Coexisting papillary thyroid carcinoma occurred in three patients with HCA. Twelve patients with HCAs had multiple lesions, five of which were bilateral. Patients with HCA were followed up for 675 patient-years, 45 for four years or more (maximum duration, 36 years). There were no recurrences or deaths among the patients with benign Hürthle cell tumors. Thus, patients with HCA had a benign course, and histologic examination results accurately reflected malignant potential.
由于这些肿瘤的恶性潜能存在争议,我们研究了1943年至1982年期间在旧金山加利福尼亚大学就诊的许特莱细胞肿瘤患者的记录。在我们的84例患者中,71例患有许特莱细胞腺瘤(HCA),9例在慢性甲状腺炎中有许特莱细胞改变,4例患有许特莱细胞癌。3例HCA患者并存甲状腺乳头状癌。12例HCA患者有多个病灶,其中5个为双侧病灶。HCA患者随访了675个患者年,45例随访4年或更长时间(最长36年)。良性许特莱细胞肿瘤患者无复发或死亡。因此,HCA患者病程呈良性,组织学检查结果准确反映了恶性潜能。