Cystic adenomatoid malformation of the lung causing hydrops fetalis: case report and review of the literature.

Abstract:

OBJECTIVE:Fetal congenital cystic adenomatoid malformation (CCAM) is a rare lung abnormality with a highly variable prognosis depended on the presence of fetal hydrops and the size of the cysts. In case of fetal hydrops the prognosis is fatal without intervention. METHODS AND DESIGN:Case report and literature review. SETTING:We report on the ultrasound and pathological findings of a hydropic fetus due to a CCAM Type II at 22 weeks of gestation. CONCLUSIONS:Congenital cystic adenomatoid malformation is a rare fetal lung disease with an excellent prognosis in the absence of fetal hydrops. CCAM associated with fetal hydrops carries a grave prognosis but survival rates of 70% can be achieved by thoraco-amniotic drainage in those with macrocystic lesions.

journal_name

Arch Gynecol Obstet

authors

Schott S,Mackensen-Haen S,Wallwiener M,Meyberg-Solomayer G,Kagan KO

doi

10.1007/s00404-008-0880-4

subject

Has Abstract

pub_date

2009-08-01 00:00:00

pages

293-6

issue

2

eissn

0932-0067

issn

1432-0711

journal_volume

280

pub_type

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