Sciubba J J, D'Amico E, Attie J N
Department of Dentistry, Long Island Jewish Medical Center, New Hyde Park, NY 11042.
J Oral Pathol. 1987 Jul;16(6):310-6. doi: 10.1111/j.1600-0714.1987.tb00700.x.
Two children with multiple endocrine neoplasia syndrome, Type IIb, (MEN IIb), whose natural mother died from complications of general anesthesia, due to undiagnosed bilateral pheochromocytomas, are described. Of particular interest is the fact that the daughter presented with many stigmata of the syndrome, including the typical facies, while her brother had no obvious clinical manifestations of the syndrome. Both children to date have undergone total thyroidectomy, and pathology reports have confirmed the presence of medullary thyroid carcinoma.
本文描述了两名患有IIb型多发性内分泌肿瘤综合征(MEN IIb)的儿童,他们的生母因双侧嗜铬细胞瘤未被诊断而死于全身麻醉并发症。特别值得注意的是,女儿表现出该综合征的许多体征,包括典型面容,而她的哥哥没有该综合征的明显临床表现。迄今为止,两名儿童均已接受甲状腺全切术,病理报告证实存在甲状腺髓样癌。