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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2022-09-29</publicationDate>
    
        <volume>15</volume>
        <issue>3</issue>

 
    <startPage>1791</startPage>
    <endPage>1795</endPage>

	 
      <doi>10.13005/bpj/2518 </doi>
        <publisherRecordId>45652</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Cystoperitoneal Shunting for Patient with Hydrocephalus Associated with Aqueductal Obstruction in Dandy-Walker Malformation: A Case Report</title>

    <authors>
	 


      <author>
       <name>I Wayan Niryana</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Steven Awyono</name>


		
	<affiliationId>2</affiliationId>

      </author>
    

	 


      <author>
       <name>Kevin Kristian Putra</name>

		
	<affiliationId>2</affiliationId>
      </author>
    

	 


      <author>
       <name>Nyoman Golden</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Neurosurgery Division, Department of Surgery, Faculty of Medicine, Universitas Udayana, Sanglah General Hospital, Bali, Indonesia</affiliationName>
    

		
		<affiliationName affiliationId="2">Neurosurgery Residency Program, Faculty of Medicine, Universitas Udayana, Sanglah General Hospital, Bali, Indonesia</affiliationName>
    
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Dandy-Walker Malformation presents  as a congenital anomaly that affects the posterior fossa. Presenting hydrocephalus as secondary to Dandy-Walker Malformation is the main concern and complication. The cyst formation in the posterior fossa obstructs the cerebrospinal flow that led to the hydrocephalus. Ideal management to treat Dandy-Walker malformation are varied. Shunting, cyst excision, and endoscopy third ventriculostomy are the proposed management.

Case Report

Presenting a case of a 1-month-age male baby who was diagnosed with vermis agenesis and posterior fossa enlargement by antenatal ultrasound. Later on, Magnetic Resonance Imaging revealed Dandy-Walker Malformation with hydrocephalus and aqueduct obstruction. Cystoperitoneal shunt was performed for this patient. Proximal shunt trajectory measured from Magnetic Resonance Imaging. As the goal of therapy is to achieve normal development, this patient needs long-term follow-up in collaboration with pediatric and physiotherapy. After 18 months of follow-up, he was able to crawl with routine and proper physiotherapy.

Conclusion

Hydrocephalus in Dandy-Walker Malformation patients related to aqueduct obstruction may be treated with a single Cystoperitoneal shunt. Aqueduct obstruction in these patients may be temporary due to high pressure on the posterior fossa that pushed the vermis forward. Cystoperitoneal shunt may reduce posterior fossa pressure and then deprive the pressure that obstructs aqueduct.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol15no3/cystoperitoneal-shunting-for-patient-with-hydrocephalus-associated-with-aqueductal-obstruction-in-dandy-walker-malformation-a-case-report/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Aqueduct Obstruction</keyword>
      

      
        <keyword> Cystoperitoneal shunt</keyword>
      

      
        <keyword> Dandy-Walker malformation</keyword>
      

      
        <keyword> Hydrocephalus</keyword>
      

      
        <keyword> Posterior Fossa Cyst Formation</keyword>
      
</keywords>
  </record>
</records>