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SQUMJ-Sultan Qaboos University Medical Journal. 2013; 13 (4): 597-600
in English | IMEMR | ID: emr-159048

ABSTRACT

Intraventricular hemangioblastoma [HB] is very rare; few cases of intraventricular HB have been reported in the literature, either sporadically or in association with von Hippel-Lindau disease. Furthermore, the incidence of ventricular haemorrhage from HB seems to be uncommon. We report a unique case of sporadic HB of the right lateral ventricle presenting with intratumoural and intraventricular haemorrhage in addition to multifocal intracranial superficial siderosis, indicating the presence of a subarachnoid haemorrhage [SAH] as well. Such a combination has not been reported before. In the future, the detection of an intraventricular mass in association with ventricular haemorrhage, with or without SAH, should include HB as a differential diagnosis, particularly when the imaging appearances are not typical of the more common intraventricular tumours


Subject(s)
Humans , Male , Cerebral Ventricles/pathology , Brain Neoplasms/pathology , Diagnosis, Differential , von Hippel-Lindau Disease , Neoplasm Metastasis , Subarachnoid Space
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