Choroid Plexus Papilloma Originating in the Sella Turcica -Case Report-
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چکیده
منابع مشابه
Giant Choroid plexus papilloma in a child: A Case Report
Tumors of the choroid plexus are rare neoplasms of neuroectodermal origin, accounting for less than 1% of all intracranial tumors. These tumors are primarily found in children, but they can be observed as well as in adults , infants and prenatal occurrence has been reported.1 In children, tumors of the choroid plexus are located most often in the lateral ventricle, but they can also be found in...
متن کاملChoroid plexus papilloma and Aicardi syndrome: case report.
A case of Aicardi syndrome associated with a choroid plexus papilloma of the third and both lateral ventricles in a 15 months old baby girl is repported. The tumor was completely removed via three craniotomies. Reports of the literature with the association of choroid plexus papilloma and Aicardi syndrome are rare. We suggest that children diagnosed with Aicardi syndrome should routinely underg...
متن کاملIntraparenchymal Choroid Plexus Papilloma: A Case Report and Literature Review
Choroid plexus papilloma (CPP) is a rare tumor of the central nervous system, which is usually located in the ventricular system and can metastasize to cisterns along the cerebrospinal fluid circulation. CPP is only rarely located in the intraparenchymal. Here, we describe an unusual case of such a tumor in a 25-yearold man. He initially experienced a sudden, generalized tonic-clonic seizure; f...
متن کاملA Case of Papilloma of the Choroid Plexus.
A girl of 7 years was admitted to the Royal Manchester Children's Hospital under Dr. Ward's care on March 12th, 1932. The history was as follows. The child had recovered from measles 3 weeks previously, since when she had taken little interest in anybody. For a fortnight she had complained of headache and of cramp-like pain in the arms and legs, and for the same period nearly all food had been ...
متن کاملChoroid plexus papilloma of the cerebellopontine angle.
Choroid plexus papillomas are rare tumors, representing less than 1% of all intracranial neoplasms in our review of the English literature. Derived from the neuroepithelial cells of the choroid plexus, these tumors recapitulate the structure of the normal choroid plexus, often demonstrating a well-developed papillary architecture. This tumor most commonly affects children and typically arises i...
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ژورنال
عنوان ژورنال: Neurologia medico-chirurgica
سال: 2010
ISSN: 0470-8105,1349-8029
DOI: 10.2176/nmc.50.144