“Acquired” Dandy–Walker malformation and cerebellar hemorrhage: Usefulness of serial MRI

2016 ◽  
Vol 20 (1) ◽  
pp. 188-191 ◽  
Author(s):  
Anna Pichiecchio ◽  
Alice Decio ◽  
Carol Di Perri ◽  
Cecilia Parazzini ◽  
Andrea Rossi ◽  
...  
2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Tadashi Shiohama ◽  
Ryo Ando ◽  
Katsunori Fujii ◽  
Hiroki Mukai ◽  
Yuki Naruke ◽  
...  

Dandy-Walker malformation (DWM) is a posterior fossa anomaly characterized by hypoplasia and upward rotation of the cerebellar vermis and cystic dilation of the fourth ventricle. The cyst of DWM rarely extends posteriorly to almost completely fill the entire posterior fossa, which mimics primary cerebellar agenesis, a cerebellar porencephalic cyst, and an arachnoid cyst due to the lack of clarity of the thin cystic wall. A 10-month-old female born at 23 weeks’ gestation with cerebellar hemorrhage in the neonatal period was admitted to our hospital with dysphagia and side-to-side head bobbing. The detection of hemosiderin deposits enveloping the cyst wall by T2 star-weighted angiography (SWAN) was useful for the differential diagnosis of an acquired form of DWM from primary cerebellar agenesis. Cyst fenestration successfully improved dysphagia and head bobbing. A pathological specimen of the perforated cyst consisted of collagen fibers with hemosiderin deposits but lacked congenital cyst components. In infants with posterior fossa cysts, SWAN will be useful for a differential diagnosis between DWM and primary cerebellar agenesis.


Author(s):  
Matthew T. Whitehead ◽  
Gilbert Vezina ◽  
Sarah D. Schlatterer ◽  
Sarah B. Mulkey ◽  
Adre J. du Plessis

1997 ◽  
Vol 16 (4) ◽  
pp. 326-328 ◽  
Author(s):  
Véronique T. Humbertclaude ◽  
Philippe A. Coubes ◽  
Nicolas Leboucq ◽  
Bernard B. Echenne

1996 ◽  
Vol 16 (12) ◽  
pp. 1137-1140 ◽  
Author(s):  
CHIH-PING CHEN ◽  
FEN-FEN LIU ◽  
SHEAU-WEN JAN ◽  
YUH-CHENG YANG ◽  
CHUNG-CHI LAN

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