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IIb型多发性内分泌肿瘤综合征:一例报告

Multiple endocrine neoplasia syndrome type IIb: a case report.

作者信息

Edwards M, Reid J S

机构信息

Department of Child Dental Health, Glasgow Dental Hospital and School NHS Trust, Scotland.

出版信息

Int J Paediatr Dent. 1998 Mar;8(1):55-60. doi: 10.1046/j.1365-263x.1998.00063.x.

Abstract

Multiple endocrine neoplasia type IIb (MEN IIb) is a syndrome, part of which can involve neoplastic change in the thyroid and adrenal glands. It has unusual oro-facial manifestations including mucosal neuromata on the lips, cheeks and tongue. A child aged 3 years and 10 months presented with mucosal tags at the corners of the mouth, early eruption of permanent teeth, malocclusion and facial asymmetry. Biopsy of the excess mucosal tissue suggested a diagnosis of either MEN type IIb or neurofibromatosis. Genetic testing eventually confirmed MEN type IIb. The patient has been followed up regularly for 9 years. He has developed modular lesions on his tongue and irregular enlargement of his lower lip, but to date there have been no signs of tumour development. This report emphasizes the importance of thorough examination of the oral mucosa and follow-up of any abnormalities.

摘要

多发性内分泌腺瘤病IIb型(MEN IIb)是一种综合征,其中一部分可涉及甲状腺和肾上腺的肿瘤性改变。它有不寻常的口面部表现,包括嘴唇、脸颊和舌部的黏膜神经瘤。一名3岁10个月大的儿童出现嘴角黏膜赘生物、恒牙早萌、错牙合畸形和面部不对称。对多余黏膜组织进行活检提示诊断为MEN IIb型或神经纤维瘤病。基因检测最终确诊为MEN IIb型。该患者已定期随访9年。他的舌头出现了结节性病变,下唇不规则增大,但迄今为止尚无肿瘤发展的迹象。本报告强调了全面检查口腔黏膜以及对任何异常情况进行随访的重要性。

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