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个体肿瘤综合征的管理。甲状腺髓样癌和甲状旁腺功能亢进。

Management of individual tumor syndromes. Medullary thyroid carcinoma and hyperparathyroidism.

作者信息

Snow K J, Boyd A E

机构信息

Division of Endocrinology, Diabetes, Metabolism, and Molecular Medicine, New England Medical Center Hospitals, Tufts University School of Medicine, Boston, Massachusetts.

出版信息

Endocrinol Metab Clin North Am. 1994 Mar;23(1):157-66.

PMID:7913022
Abstract

Significant advances have been made in the understanding of the pathophysiology and the ability to effectively screen for and treat medullary thyroid carcinoma. The parafollicular cells, or C-cells, are the cell of origin for medullary thyroid carcinoma. C-cell hyperplasia is a premalignant disease that progresses rapidly to medullary thyroid carcinoma. C-cells produce calcitonin, which serves as a marker to prospectively screen patients for C-cell disease. One major concern in screening for this disease has been the incidence of false positive results. This problem is addressed in light of new, more stringent criteria for the diagnosis of C-cell hyperplasia. The association of hyperparathyroidism with MEN 2 is discussed with evidence that thyroidectomy of C-cell disease may affect the incidence of parathyroid disease.

摘要

在甲状腺髓样癌的病理生理学认识以及有效筛查和治疗能力方面已经取得了重大进展。甲状腺滤泡旁细胞,即C细胞,是甲状腺髓样癌的起源细胞。C细胞增生是一种癌前疾病,可迅速发展为甲状腺髓样癌。C细胞产生降钙素,它可作为前瞻性筛查C细胞疾病患者的标志物。筛查这种疾病的一个主要问题是假阳性结果的发生率。根据新的、更严格的C细胞增生诊断标准解决了这个问题。讨论了甲状旁腺功能亢进与MEN 2的关联,并有证据表明C细胞疾病的甲状腺切除术可能会影响甲状旁腺疾病的发生率。

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