Hansen O P, Hansen M, Hansen H H, Rose B
Acta Med Scand. 1976;200(4):327-31. doi: 10.1111/j.0954-6820.1976.tb08240.x.
A case of multiple endocrine adenomatosis (MEA) of mixed type is presented. The syndrome, observed in a 65 year-old female, consisted of multiple neurofibroadenomatosis, medullary thyroid carcinoma, multiple adenomata of the parathyroids, adrenal cortical adenoma and small cell anaplastic bronchogenic carcinoma. Thus, it was composed of type 1 as well as of type 2 MEA. On the basis of another seven cases, collected from the literature, the MEA syndrome of mixed type is reviewed with special reference to the phylogenetic origin of the cells of the APUD system.
本文报告一例混合型多发性内分泌腺瘤病(MEA)。该综合征见于一名65岁女性,包括多发性神经纤维瘤病、甲状腺髓样癌、甲状旁腺多发性腺瘤、肾上腺皮质腺瘤和小细胞间变性支气管源性癌。因此,它由1型和2型MEA组成。基于从文献中收集的另外七例病例,对混合型MEA综合征进行了综述,并特别参考了APUD系统细胞的系统发生起源。