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婴儿期甲状腺发育异常性肿瘤:两例报告

Dysontogenetic neoplasms of the thyroid gland in infancy: two case reports.

作者信息

Pinelli V, Pierro V, Bottero S, Marsella P, Camarda M

出版信息

Int J Pediatr Otorhinolaryngol. 1985 Oct;10(1):101-10. doi: 10.1016/s0165-5876(85)80063-x.

Abstract

Two rare cases of benign dysontogenetic neoplasms of the thyroid gland in pediatric age are presented, which were observed at the E.N.T. department of the Bambino Gesù Hospital of Rome, and successfully operated. The first case turned out to be a dysembryoma, classified as monodermic because of its origin from derivatives of only one germinal layer, the entoderm. The second case, a teratoma, presented a high seric concentration of AFP as the consequence of the synthetic activity of the share of embryonal epatic tissue present in the neoformation. Criteria to distinguish thyroid from cervical teratomata and to classify the different types of dysontogenetic neoplasms are discussed. The usual clinical and pathological manifestations of teratomas of the neck in infancy are mentioned. The necessity of a prompt surgical removal and of pre- and postoperative thyroid function studies is mentioned.

摘要

本文介绍了两例小儿甲状腺良性发育异常性肿瘤的罕见病例,这两例病例均在罗马的圣婴儿童医院耳鼻喉科被观察到,并成功进行了手术。第一例病例是一个胚胎瘤,因其仅起源于一个胚层即内胚层的衍生物,故被归类为单胚层的。第二例病例是一个畸胎瘤,由于肿瘤中存在的胚胎肝组织部分的合成活性,导致血清甲胎蛋白浓度升高。文中讨论了区分甲状腺肿瘤与颈部畸胎瘤以及对不同类型发育异常性肿瘤进行分类的标准。文中还提到了婴儿期颈部畸胎瘤常见的临床和病理表现。文中指出了及时进行手术切除以及术前和术后甲状腺功能研究的必要性。

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