Neurocutaneous Melanosis: Prenatal Presentation as a Posterior Fossa Cyst

2021 ◽  
Author(s):  
James E. East ◽  
Bruno P. Soares
2011 ◽  
Vol 7 (5) ◽  
pp. 549-556 ◽  
Author(s):  
Daniel H. Fulkerson ◽  
Todd D. Vogel ◽  
Abdul A. Baker ◽  
Neal B. Patel ◽  
Laurie L. Ackerman ◽  
...  

Object The optimal treatment of symptomatic posterior fossa arachnoid cysts is controversial. Current options include open or endoscopic resection, fenestration, or cyst-peritoneal shunt placement. There are potential drawbacks with all options. Previous authors have described stenting a cyst into the ventricular system for supratentorial lesions. The current authors have used a similar strategy for posterior fossa cysts. Methods The authors performed a retrospective review of 79 consecutive patients (1993–2010) with surgically treated intracranial arachnoid cysts. Results The authors identified 3 patients who underwent placement of a stent from a posterior fossa arachnoid cyst to a supratentorial ventricle. In 2 patients the stent construct consisted of a catheter placed into a posterior fossa arachnoid cyst and connecting to a lateral ventricle catheter. Both patients underwent stent placement as a salvage procedure after failure of open surgical fenestration. In the third patient a single-catheter cyst-ventricle stent was stereotactically placed. All 3 patients improved clinically. Two patients remained asymptomatic, with radiographic stability in a follow-up period of 1 and 5 years, respectively. The third patient experienced initial symptom resolution with a demonstrable reduction of intracystic pressure. However, he developed recurrent headaches after 2 years. Conclusions Posterior fossa cyst–ventricle stenting offers the benefits of ease of surgical technique and a low morbidity rate. It may also potentially reduce the incidence of shunt-related headaches by equalizing the pressure between the posterior fossa and the supratentorial compartments. While fenestration is considered the first-line therapy for most symptomatic arachnoid cysts, the authors consider cyst-ventricle stenting to be a valuable additional strategy in treating these rare and often difficult lesions.


2019 ◽  
pp. 239-245
Author(s):  
Peter J. Morone ◽  
John C. Wellons

A Dandy-Walker malformation is an anatomical triad characterized by a large posterior fossa, agenesis of the cerebellar vermis, and dilation of the 4th ventricle. Up to 90% of patients will have hydrocephalus secondary to obstruction of fourth ventricular outflow through the foramen of Luschka and Magendie. The differential diagnosis of Dandy-Walker malformation includes Blake’s pouch cyst, a cystic structure originating within the roof of the 4th ventricle that herniates into the cisterna magna, and posterior fossa arachnoid cysts, which typically displace both the cerebellum and 4th ventricle anteriorly and demonstrate a propensity to enlarge. Brain MRI is the best diagnostic imaging modality to evaluate posterior fossa anatomy and cystic structures. Not all posterior fossa cysts require treatment. Indications for surgical intervention include enlargement, symptomatic mass effect and/or hydrocephalus.


1976 ◽  
Vol 4 (1) ◽  
pp. 29-30 ◽  
Author(s):  
Timothy G. Lee ◽  
Burritt W. Newton

1997 ◽  
Vol 86 (5) ◽  
pp. 907 ◽  
Author(s):  
Tomoo Tokime ◽  
Shinichiro Okamoto ◽  
Sen Yamagata ◽  
Tsuneki Konishi

2005 ◽  
Vol 20 (6) ◽  
pp. 524-527 ◽  
Author(s):  
Mehmet Teksam ◽  
Umut Ozyer ◽  
Alexander McKinney ◽  
Ismail Kirbas ◽  
Banu Cakir

1987 ◽  
Vol 28 (3) ◽  
pp. 215-220 ◽  
Author(s):  
Arthur N. Wang ◽  
Benjamin S. Carson

Author(s):  
Sandip Ojha ◽  
Aditya Singhal ◽  
Sandesh Shrestha ◽  
Prasanta Poudyal

<p class="abstract">Dandy-Walker variant (DWV) has been used to describe a combination of cystic dilation of the fourth ventricle and hypoplastic cerebellar vermis in the absence of an enlargement of the posterior fossa. Magnetic resonance imaging (MRI) is the modality of choice for diagnosing DWV. But it can also be diagnosed by evaluating the subject clinically and by CT scans. We presented here a case report of a patient with DWV who was diagnosed by clinical evaluation and CT scans. A 15 years old girl presented with the symptoms of pain and ear discharge from both ears. She had developmental delay, mental retardation and poor nutritional status. The CT scan of the patient showed a posterior fossa cyst with hypoplastic vermis and communicating hydrocephalus without obvious enlargement of the posterior fossa. Hence, a diagnosis of DWV was made. For the ear pathology, she underwent modified radical mastoidectomy and other medical treatments.</p>


1991 ◽  
Vol 19 (7) ◽  
pp. 434-437 ◽  
Author(s):  
S. Raman ◽  
S. P. Rachagan ◽  
C. T. Lim

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