Isolated posterior fossa hypertension and brainstem compression caused by entrapped Dandy-Walker cyst: a case report.

نویسندگان

  • NaimU Rahman
  • A Jamjoom
  • Z A Jamjoom
چکیده

Lateral ventricular shunting alone is often considered to be adequate treatment for hydrocephalus caused by Dandy-Walker syndrome. A patient is presented in whom progressive spastic tetraparesis and signs of severe brainstem compression developed due to an entrapped posterior fossa cysts, in spite of an adequately functioning lateral ventricular shunt. Addition of a cystoperitoneal shunt resulted in rapid resolution of symptoms and deficits. This case illustrates that potentially fatal brainstem compression and dangerous posterior fossa hypertension may develop if the posterior fossa cyst does not communicate with the lateral ventricles, where the shunt is placed.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

گزارش یک مورد سندرم دندی واکر در یک نوزاد

ABSTRACT Dandy-Walker syndrom was described by blackfan, dandy in 1914. Dandy-Walker syndrome is characterized by a triad of complete or partial agenesis of the cerebellar vermis, cystic dilatation of the forth ventricle and enlarged posterior fossa with upward displacement of the transvers sinus, tentorium and torcular. The most striking abnormality is the presence of a huge dilated f...

متن کامل

Association of Dandy-Walker Malformation and Neurocutaneous Melanosis in a Newborn: A Case Report

Background: This case report presents a very rare Dandy-Walker malformation (DWM) in association with a sporadic condition characterized by congenital melanocytic nevi and melanocytic thickening of the leptomeninges called Neurocutaneous melanosis (NCM). The DWM is a rare congenital disorder characterized by enlarged posterior fossa and a cystic enlargement of the four...

متن کامل

Asymptomatic Dandy-Walker syndrome in an adult

This 34 years old man presented with moderate and persistent headache occurring 48 hours following Benin head injury. There were no symptoms of increased intracranial pressure. Neurological examination was unremarkable without cerebellar ataxia or psychomotor retardation .the patient was submitted to CT scan and magnetic resonance imaging (MRI) of the brain that revealed agenesis of cerebellar ...

متن کامل

Extensive intracranial calcification of pseudo-TORCH syndrome with features of Dandy–Walker malformation

Pseudo-TORCH syndrome or congenital infection-like syndrome is a group of conditions which resemble congenital infections such as those caused by toxoplasmosis, rubella, cytomegalovirus (CMV), herpes (TORCH) group of organisms, clinico-radiologically, but serological tests are negative for the organisms. One of the variety shows features such as microcephaly, extensive intracranial calcificatio...

متن کامل

Spontaneous resolution of Blake’s pouch cyst

Blake's pouch cyst is a rare posterior fossa cystic lesion characterized by posterior ballooning of the superior medullary velum into the cisterna magna. It must be differentiated from severe malformations like inferior vermian hypoplasia and Dandy Walker malformation. We describe a case in which a diagnosis of Blake's pouch cyst was made on prenatal ultrasound and later confirmed by MRI. The c...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • JPMA. The Journal of the Pakistan Medical Association

دوره 45 7  شماره 

صفحات  -

تاریخ انتشار 1995