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[甲状腺髓样癌——家族性疾病还是散发性疾病?]

[Medullary thyroid carcinoma--familial or sporadic disease?].

作者信息

Høie J, Jørgensen O G, Nesland J M, Møller P, Bjøro K

机构信息

Avdeling for kirurgisk onkologi, Det Norske Radiumhospital, Oslo.

出版信息

Tidsskr Nor Laegeforen. 1994 Oct 20;114(25):2951-4.

PMID:7974404
Abstract

Medullary thyroid cancer may be autosomal dominantly inherited. Calcitonin is a very sensitive tumour marker in medullary thyroid cancer. It is essential to measure calcitonin in first grade relatives of these patients, in order to expose familial incidents of subclinical disease. In 55 patients with medullary thyroid cancer and no history of familial disease, nine close relatives with elevated calcitonin were identified in four different families. Eight of these nine have been thyroidectomized. Five were found to have medullary thyroid cancer, one had definite C-cell-hyperplasia, and two had equivocal C-cell hyperplasia. The last two, had elevated basal serum calcitonin-levels were increased, but with no further increase after intravenous pentagastrin bolus injection. Thyroidectomy did not modify these results and DNA-analysis may be necessary to draw a conclusion about the hereditary situation of these patients.

摘要

甲状腺髓样癌可能为常染色体显性遗传。降钙素是甲状腺髓样癌中一种非常敏感的肿瘤标志物。对这些患者的一级亲属进行降钙素检测至关重要,以便发现亚临床疾病的家族性发病情况。在55例无家族性疾病史的甲状腺髓样癌患者中,在4个不同家庭中发现9名降钙素升高的近亲。这9人中的8人已接受甲状腺切除术。其中5人被发现患有甲状腺髓样癌,1人有明确的C细胞增生,2人有可疑的C细胞增生。最后两人基础血清降钙素水平升高,但静脉注射五肽胃泌素后无进一步升高。甲状腺切除术并未改变这些结果,可能需要进行DNA分析才能得出这些患者遗传情况的结论。

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