Journal of Japan Society of Perinatal and Neonatal Medicine
Online ISSN : 2435-4996
Print ISSN : 1348-964X
Case reports
A case of amniotic band syndrome with extensive acrania
Konosuke SuzukiYukiko ToyaAtsushi MatsumotoShigekuni TsuchiyaNao TakashimizuYu KonishiGenichiro SotodateSachiko TanifujiManami Akasaka
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2023 Volume 59 Issue 1 Pages 62-66

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Abstract

 We report a case of a male infant born at 38 weeks and 0 days of gestation. The patient was referred to our hospital after suspicion of acrania by fetal ultrasonography at 25 weeks. The cranium could be identified only up to the frontal region, and the brain tissue was floating in the amniotic fluid, surrounded by membrane-like structures. The patient was born by cesarean section and was found to have acrania, encephalocele, phalangeal defect, and strangulated ring. Placental pathology showed extensive omental defects, and a diagnosis of anencephaly due to amniotic band syndrome was made. We administered medical treatment for convulsive seizures and infections associated with spinal fluid leakage from the head. The patient underwent encephalocele repair and ventriculoperitoneal shunting for encephalocele and ventricular enlargement, respectively, at the age of 1 year and 9 months. The patient is currently being managed at home. Prenatally diagnosed cases of widespread anencephaly often lead to pregnancy interruption and fetal death. The possibility of long-term survival is suggested for acrania without anencephaly and other major visceral abnormalities. Accumulation of further cases is warranted.

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© 2023 Journal of Japan Society of Perinatal and Neonatal Medicine
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