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[家族性髓样癌的诊断]

[Diagnosis of familial medullary cancers].

作者信息

Argémi B, Vagneur J P, Cannoni M, Charpin C, Even F, Rollat M C, Bollet C

出版信息

Biomed Pharmacother. 1984;38(5):270-2.

PMID:6525427
Abstract

Medullary thyroid carcinoma (MTC) is hereditary in 20 to 25% of cases. It is inherited as an autosomal dominant trait. MTC can be considered as a sporadic form only after a clinical and biological survey of the two parents, siblings and children of the patient, using pentagastrin stimulation test. The authors have studied 36 patients from 26 families. Hereditary MTC with different clinical features, were discovered in two kindreds. The systematic investigation leads to the discovery of 7 cases in the first family, and of 3 in the second. The treatment of the disease at the first stage of its evolution has been possible when an early diagnosis had been made, such as in the second family.

摘要

甲状腺髓样癌(MTC)在20%至25%的病例中具有遗传性。它作为常染色体显性性状遗传。只有在对患者的双亲、兄弟姐妹及子女进行临床和生物学检查,并采用五肽胃泌素刺激试验后,MTC才能被视为散发型。作者研究了来自26个家庭的36例患者。在两个家族中发现了具有不同临床特征的遗传性MTC。系统调查在第一个家族中发现了7例,在第二个家族中发现了3例。如在第二个家族中那样,当做出早期诊断时,在疾病演变的第一阶段对其进行治疗是可行的。

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