Massive hemorrhage is a very uncommon event among hemangioblastomas. Forty-four cases have been reported before this review. Thorough analysis of all reported cases on literature was accomplished. The majority presented as parenchymatous or subarachnoid bleedings. Subarachnoid hemorrhage was only associated with spinal hemangioblastomas, while parenchymatous bleedings were more, but not only, originated from cranial instances. Ventricular hemorrhage from a hemangioblastoma was exceptional, with only two previous cases bleeding directly into the ventricular compartment. To our knowledge, the illustrative case is the first one of pure tetraventricular hemorrhage from a hemangioblastoma. When hemangioblastoma bleeding occurs, it is usually the very first clinical presentation of a previously undetected tumor. Solid type, large size, and spinal-radicular locations are more frequently related to hemorrhage. Hemorrhage following hemangioblastoma embolization and the association of this tumor with other bleeding lesions, such as arteriovenous malformations and aneurysms, is also discussed.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10143-009-0217-1DOI Listing

Publication Analysis

Top Keywords

hemorrhage hemangioblastoma
12
massive hemorrhage
8
hemorrhage
6
hemorrhage hemangioblastomas
4
hemangioblastomas literature
4
literature review
4
review massive
4
hemorrhage uncommon
4
uncommon event
4
event hemangioblastomas
4

Similar Publications

Purpose: To demonstrate the response of a juxtapapillary retinal hemangioblastoma (JRH) to belzutifan in a patient with Von-Hippel-Lindau syndrome (VHL).

Methods: This case report includes fundus photography and optical coherence tomography to compare a juxtapapillary retinal hemangioblastoma (JRH) before and 24 months after treatment with belzutifan.

Results: An 18-year-old woman with VHL was diagnosed with a juxtapapillary retinal hemangioblastoma (JRH) at age 13.

View Article and Find Full Text PDF
Article Synopsis
  • Hemangioblastoma is a rare type of spinal cord tumor, making up only 1-5% of such cases, particularly notable in this report is the cervical intradural extramedullary hemangioblastoma without Von Hippel-Lindau syndrome, which has never been documented in China before.
  • A 53-year-old male presented with symptoms including mild right hemiplegia, and imaging confirmed the tumor at the cervical spine; pre-surgery angiography helped minimize bleeding during the complete resection of the tumor.
  • Post-surgery, the patient showed improved motor and sensory functions, and pathology confirmed the tumor type; findings aligned with literature indicating combined surgical approaches are best for managing this rare condition while reducing risks associated with
View Article and Find Full Text PDF

Early identification of patients at risk with von Hippel-Lindau (VHL) syndrome-related pheochromocytoma and paraganglioma (PPGL) is crucial to prevent morbidity. We investigated the current surveillance recommendations in VHL-related PPGL in children and adolescents. German Pediatric Oncology and Hematology-Malignant Endocrine Tumor registry (GPOH-MET) and Freiburg-VHL registry (1996-2022).

View Article and Find Full Text PDF
Article Synopsis
  • Von Hippel-Lindau is a rare genetic disorder with an autosomal dominant inheritance pattern, leading to multiple vascular tumors, especially in the brain, eyes, and organs.
  • The disease can manifest at any age, with retinal tumors often being one of the first signs; MRI and fluorescein angiography are key diagnostic tools.
  • A case study highlights a woman in her late 30s with vision loss, revealing various eye and kidney abnormalities, including cystic lesions in her brain and elevated urine protein levels.
View Article and Find Full Text PDF

Pediatric Spinal Vascular Abnormalities: Overview, Diagnosis, and Management.

Neuroimaging Clin N Am

November 2024

Department of Radiology, Neurology & Neurosurgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Section of Interventional Neuroradiology, Department of Radiology, Northwestern Memorial Hospital, 676 North Street, Clair street, Suite 1400, Chicago, IL 60611, USA.

Article Synopsis
  • * Spinal cord hemangioblastomas make up a small percentage (1.1% to 2.4%) of central nervous system tumors, typically presenting as single tumors in adults around their 40s, while they are rare in children, especially those without VHL syndrome.
  • * The thoracic spinal cord is the most common location for these tumors, which can lead to serious symptoms like spinal cord compression and bleeding, despite being classified as benign.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!