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[颈部囊状水瘤与非免疫性胎儿水肿]

[Cystic hygroma of the neck and non-immunologic hydrops fetalis].

作者信息

Schmid G, Gembruch U, Hansmann M, Kowalewski S

机构信息

Universitäts-Kinderklinik, Bonn.

出版信息

Monatsschr Kinderheilkd. 1987 Aug;135(8):518-21.

PMID:3309629
Abstract

Fetal cystic hygromas are a manifestation of early lymphatic obstruction. They are mostly associated with nonimmune hydrops fetalis. They often occur in a number of chromosome abnormalities (Turner syndrome and Down syndrome). We report on a prenatally detected case with nuchal cystic hygroma and nonimmune hydrops fetalis without chromosome aberration and without further major malformations. Postnatally hygroma and hydrops regressed.

摘要

胎儿囊状水瘤是早期淋巴管阻塞的一种表现。它们大多与胎儿非免疫性水肿相关。它们常发生于多种染色体异常(特纳综合征和唐氏综合征)。我们报告一例产前检测到的伴有颈部囊状水瘤和胎儿非免疫性水肿的病例,该病例无染色体畸变且无其他严重畸形。出生后,水瘤和水肿消退。

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1
[Cystic hygroma of the neck and non-immunologic hydrops fetalis].[颈部囊状水瘤与非免疫性胎儿水肿]
Monatsschr Kinderheilkd. 1987 Aug;135(8):518-21.
2
[Sonographic detection of hygroma colli in the fetus].[胎儿颈部水囊瘤的超声检测]
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Spontaneous resolution of fetal cystic hygroma and hydrops in Turner syndrome.Turner综合征中胎儿囊状水瘤和水肿的自然消退
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A case report of Turner syndrome associated with fetal nuchal cystic hygroma and bilateral syndactyly of the hands and feet.特纳综合征合并胎儿颈项透明层囊状水肿及手足并指(趾)畸形 1 例报告
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