Results 41 to 50 of about 222,552 (156)
Choroid plexus tumours are rare, intraventricular, primary central nervous system tumours derived from the choroid plexus epithelium. They occur predominantly in children and are classified based on histological criteria as choroid plexus papilloma ...
Maria Santos +3 more
core +1 more source
An overview of the European standard clinical practice recommendations for choroid plexus tumours
Choroid plexus tumours (CPT) are rare epithelial brain tumours that primarily affect very young children. They can be classified as benign choroid plexus papilloma (CPP, WHO grade 1), intermediate grade atypical choroid plexus papilloma (aCPP, WHO grade ...
David King +16 more
doaj +1 more source
Congenital Intracranial Tumors: Prenatal Diagnosis by Fetal Magnetic Resonance Imaging
Fetal intracranial tumors are rare, comprising 0.5%–1.9% of all childhood tumors, with their true incidence potentially underestimated. This review highlights the role of fetal MRI, particularly with advanced sequences, in diagnosing common fetal brain tumors such as teratomas, astrocytomas, and choroid plexus papillomas, often presenting unique ...
Jing‐Ya Ren +3 more
wiley +1 more source
Choroid plexus papilloma of bilateral lateral ventricle
PubMedID: 12601462Background. Choroid plexus papillomas are rare, accounting for less than 1% of all intracranial tumours in adults. However, they are relatively more common in childhood and constitute 1.5 to 4% of intracranial tumours.
Tuna M. +6 more
core +1 more source
Choroid-Plexus Papilloma of the Cerebellopontine Angle
We report a case of a transdural choroid plexus papilloma of the cerebellopontine angle in a 23-year-old woman. Choroid plexus papillomas are rare intracranial tumors, usually occurring intraventricularly.
Panizza, BJ +3 more
core +1 more source
ABSTRACT A critical clinical consideration, in addition to other common risk factors predisposing individuals to idiopathic intracranial hypertension (IIH), involves the potential co‐occurrence of increased intracranial pressure and elevated cerebrospinal fluid protein levels in the presence of underlying malignancies.
Shiva Sareh +8 more
wiley +1 more source
Posterior pituitary tumors and other rare entities involving the pituitary gland
Abstract Non‐neuroendocrine tumors account for around 10% of all primary neoplasms of the sella. If meningiomas, craniopharyngiomas, and germ cell tumors are excluded, the remaining lesions include a broad spectrum of uncommon, benign, and aggressive, often diagnostically challenging lesions.
Federico Roncaroli, Caterina Giannini
wiley +1 more source
Developing a nomogram based on SEER database for predicting prognosis in choroid plexus tumors
Choroid plexus tumors (CPT) are rare and highly vascularized neoplasms that have three histologically confirmed diagnoses, including choroid plexus papilloma, atypical choroid plexus papilloma, and choroid plexus carcinoma (CPC).
Zedi Yang +8 more
doaj +1 more source
First report of occurrence of choroid plexus papilloma and medulloblastoma in the same patient
Introduction: Choroid plexus papilloma is a benign epithelial brain tumour showing a striking predilection for infants and occurring most frequently in the lateral and fourth ventricles.
Brundler, Marie Anne +2 more
core +1 more source
INTRODUCTION: Choroid plexus tumors are rare neuroectodermal tumors that arise from the choroid plexus. Choroid plexus papillomas (CPPs) represent the lowest grade of these types of tumors and have a WHO grade I designation.
Mazur-Hart, David J +6 more
core +1 more source

