A case with congenital hydrocephaly and West syndrome who recovered from hypsarrhythmia after the resolution of shunt trouble

J. Hattori, H. Yoshinaga, N. Murakami, E. Oka, M. Kawauchi, T. Ohmoto

Research output: Contribution to journalArticle

Abstract

Hydrocephalus occasionally causes West syndrome, but the mechanism is unknown. We experienced a case with West syndrome and congenital hydrocephaly, in which the EEG findings improved after the resolution of shunt complications. The course of this case implied the pathogenesis of West syndrome associated with congenital hydrocephaly, as well as the origin of the seizures and that of the EEG findings in West syndrome. A 7-month-old girl had congenital hydrocephaly. A prenatal diagnosis was made by ultrasonography, and ventricle-peritoneal shunting was performed 7 days after birth. During the following 7 months several shunt replacements were done because of recurrent shunt complications. Her first series of infantile spasms began at the age of 6 months, and treatment was started under the diagnosis of West syndrome. One month later, her seizures were controlled by pyridoxal phosphate, while the EEG still showed hypsarrythmia. Her shunt was then removed again, because of bacterial meningitis due to shunt infection. The recovery from shunt complication resulted in marked improvement of the hypsarrhythmia. Our experience and previous literature suggest the involvement of cerebral cortex in the occurrence of West syndrome associated with congenital hydrocephaly.

Original languageEnglish
Pages (from-to)341-345
Number of pages5
JournalNo To Hattatsu
Volume32
Issue number4
Publication statusPublished - 2000

Fingerprint

Infantile Spasms
Hydrocephalus
Electroencephalography
Seizures
Pyridoxal Phosphate
Bacterial Meningitides
Prenatal Diagnosis
Cerebral Cortex
Ultrasonography
Parturition

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health

Cite this

Hattori, J., Yoshinaga, H., Murakami, N., Oka, E., Kawauchi, M., & Ohmoto, T. (2000). A case with congenital hydrocephaly and West syndrome who recovered from hypsarrhythmia after the resolution of shunt trouble. No To Hattatsu, 32(4), 341-345.

A case with congenital hydrocephaly and West syndrome who recovered from hypsarrhythmia after the resolution of shunt trouble. / Hattori, J.; Yoshinaga, H.; Murakami, N.; Oka, E.; Kawauchi, M.; Ohmoto, T.

In: No To Hattatsu, Vol. 32, No. 4, 2000, p. 341-345.

Research output: Contribution to journalArticle

Hattori, J, Yoshinaga, H, Murakami, N, Oka, E, Kawauchi, M & Ohmoto, T 2000, 'A case with congenital hydrocephaly and West syndrome who recovered from hypsarrhythmia after the resolution of shunt trouble', No To Hattatsu, vol. 32, no. 4, pp. 341-345.
Hattori, J. ; Yoshinaga, H. ; Murakami, N. ; Oka, E. ; Kawauchi, M. ; Ohmoto, T. / A case with congenital hydrocephaly and West syndrome who recovered from hypsarrhythmia after the resolution of shunt trouble. In: No To Hattatsu. 2000 ; Vol. 32, No. 4. pp. 341-345.
@article{eb4dc0daff5f4ed9bd6e599341059314,
title = "A case with congenital hydrocephaly and West syndrome who recovered from hypsarrhythmia after the resolution of shunt trouble",
abstract = "Hydrocephalus occasionally causes West syndrome, but the mechanism is unknown. We experienced a case with West syndrome and congenital hydrocephaly, in which the EEG findings improved after the resolution of shunt complications. The course of this case implied the pathogenesis of West syndrome associated with congenital hydrocephaly, as well as the origin of the seizures and that of the EEG findings in West syndrome. A 7-month-old girl had congenital hydrocephaly. A prenatal diagnosis was made by ultrasonography, and ventricle-peritoneal shunting was performed 7 days after birth. During the following 7 months several shunt replacements were done because of recurrent shunt complications. Her first series of infantile spasms began at the age of 6 months, and treatment was started under the diagnosis of West syndrome. One month later, her seizures were controlled by pyridoxal phosphate, while the EEG still showed hypsarrythmia. Her shunt was then removed again, because of bacterial meningitis due to shunt infection. The recovery from shunt complication resulted in marked improvement of the hypsarrhythmia. Our experience and previous literature suggest the involvement of cerebral cortex in the occurrence of West syndrome associated with congenital hydrocephaly.",
author = "J. Hattori and H. Yoshinaga and N. Murakami and E. Oka and M. Kawauchi and T. Ohmoto",
year = "2000",
language = "English",
volume = "32",
pages = "341--345",
journal = "No To Hattatsu",
issn = "0029-0831",
publisher = "Japanese Society of Child Neurology",
number = "4",

}

TY - JOUR

T1 - A case with congenital hydrocephaly and West syndrome who recovered from hypsarrhythmia after the resolution of shunt trouble

AU - Hattori, J.

AU - Yoshinaga, H.

AU - Murakami, N.

AU - Oka, E.

AU - Kawauchi, M.

AU - Ohmoto, T.

PY - 2000

Y1 - 2000

N2 - Hydrocephalus occasionally causes West syndrome, but the mechanism is unknown. We experienced a case with West syndrome and congenital hydrocephaly, in which the EEG findings improved after the resolution of shunt complications. The course of this case implied the pathogenesis of West syndrome associated with congenital hydrocephaly, as well as the origin of the seizures and that of the EEG findings in West syndrome. A 7-month-old girl had congenital hydrocephaly. A prenatal diagnosis was made by ultrasonography, and ventricle-peritoneal shunting was performed 7 days after birth. During the following 7 months several shunt replacements were done because of recurrent shunt complications. Her first series of infantile spasms began at the age of 6 months, and treatment was started under the diagnosis of West syndrome. One month later, her seizures were controlled by pyridoxal phosphate, while the EEG still showed hypsarrythmia. Her shunt was then removed again, because of bacterial meningitis due to shunt infection. The recovery from shunt complication resulted in marked improvement of the hypsarrhythmia. Our experience and previous literature suggest the involvement of cerebral cortex in the occurrence of West syndrome associated with congenital hydrocephaly.

AB - Hydrocephalus occasionally causes West syndrome, but the mechanism is unknown. We experienced a case with West syndrome and congenital hydrocephaly, in which the EEG findings improved after the resolution of shunt complications. The course of this case implied the pathogenesis of West syndrome associated with congenital hydrocephaly, as well as the origin of the seizures and that of the EEG findings in West syndrome. A 7-month-old girl had congenital hydrocephaly. A prenatal diagnosis was made by ultrasonography, and ventricle-peritoneal shunting was performed 7 days after birth. During the following 7 months several shunt replacements were done because of recurrent shunt complications. Her first series of infantile spasms began at the age of 6 months, and treatment was started under the diagnosis of West syndrome. One month later, her seizures were controlled by pyridoxal phosphate, while the EEG still showed hypsarrythmia. Her shunt was then removed again, because of bacterial meningitis due to shunt infection. The recovery from shunt complication resulted in marked improvement of the hypsarrhythmia. Our experience and previous literature suggest the involvement of cerebral cortex in the occurrence of West syndrome associated with congenital hydrocephaly.

UR - http://www.scopus.com/inward/record.url?scp=0033925944&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0033925944&partnerID=8YFLogxK

M3 - Article

C2 - 10916375

AN - SCOPUS:0033925944

VL - 32

SP - 341

EP - 345

JO - No To Hattatsu

JF - No To Hattatsu

SN - 0029-0831

IS - 4

ER -