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Late‐onset isolated cystic hygroma: The obstetrical significance, management, and outcome
Author(s) -
Goldstein Israel,
Jakobi Peter,
Shoshany Gideon,
Filmer Shlomo,
Itskoviz Ioseph,
Maor Bar
Publication year - 1994
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.1970140818
Subject(s) - cystic hygroma , medicine , caesarean section , prenatal diagnosis , pregnancy , pediatrics , retrospective cohort study , surgery , obstetrics , fetus , genetics , biology
We add two cases of prenatally diagnosed late‐onset isolated cystic hygroma to the eight cases reported previously in the English literature. The obstetrical significance, management, and outcome of this entity are reviewed. A retrospective study of late‐onset isolated cystic hygromas delivered in one medical centre between 1978 and 1992 was made. The medical records of these newborns served as the basis of the present report. A Medline search of the English literature was carried out. Over a period of 15 years, we observed 11 cases of late‐onset congenital isolated cystic hygroma, two of whom had prenatal sonographic diagnosis. In one case, a Caesarean section was performed due to a huge lesion. All cases underwent surgical excision with a favourable outcome. Of the eight prenatally diagnosed cases reported previously, one died at birth due to inability to ventilate and two required a tracheostomy. Late‐onset isolated cystic hygroma should be differentiated from the early‐onset nuchal cystic hygroma. The differential diagnosis is important, as late‐onset isolated cystic hygroma does not require any prenatal intervention, but special awareness during labour and Caesarean section in extreme cases. Transport to a perinatal centre with expert neonatal, respiratory, and paediatric surgical care is recommended. The prognosis in general is favourable.

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