Sporadic Lateral Ventricular Hemangioblastoma Presenting with Intraventricular and Subarachnoid Haemorrhage = ورم أرومي وعائي فردي في البطين الوحشي ظهر بنزف داخل البطين و نزف تحت العنكبوتية

Al-Najar, Mahasen; Al-Hadidy, Azmy M.; Saleh, Ahmed A.; Altamimi, Ahmad Mousa; Al-Darawish, Asaad; Obeidat, Firas

doi:10.12816/0003324

Cited by 9 publications

(4 citation statements)

References 11 publications

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“…[ 16 ] On reviewing the literature from 1902 to 2014, we found 57 cases of supratentorial HBL without VHL as shown in Table 1 . [ 6 8 9 15 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 ] On reviewing the literature, we found that supratentorial HBL affected patients ranging from 3 months to 80 years with maximum cases belonging to 20–30 years and 40–50 years age group. Among the infants, only one case was found, thus making it a rare tumor in infancy.…”

Section: Discussion and Review Of Literaturementioning

confidence: 99%

“…Supratentorial HBL is a rare and benign neoplasm with a favorable prognosis. Being a rare entity, not much clinical [61] 21/male 2013 Frontal Cystic Kishore et al [62] 50/male 2013 Parietal Cystic with peripheral solid nodule Al-Najar et al [63] 2013 Lateral ventricle Xie et al [64] 64/female 2013 Suprasellar Solid Raghava et al [65] 50/male 2014 Frontal Solid Present study 39/male 2015 Parietal Cystic NA -Not available; VHL -Von Hippel-Lindau…”

Section: Discussionmentioning

confidence: 99%

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Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature

Pandey

Sharma

Pandey³

et al. 2016

Asian J Neurosurg

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Supratentorial hemangioblastomas (HBLs) are rare, benign vascular tumors of the central nervous system neoplasms. Very scarce literature is available regarding supratentorial HBL without von Hippel–Lindau (VHL) syndrome in an adult. We reviewed the literature and PubMed advanced search showed only a few results of supratentorial HBL without VHL syndrome. We reported a rare case of cystic supratentorial HBL in 39-year-old male affecting the parietal lobe without VHL syndrome. Supratentorial HBL is a rare tumor and supratentorial HBL without VHL syndrome are even rarer. Being a rare entity, not much clinical data is currently available regarding supratentorial HBLs, thus necessitating the need for further reporting and review of such cases.

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Section: Discussion and Review Of Literaturementioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature

Pandey

Sharma

Pandey³

et al. 2016

Asian J Neurosurg

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“…The main clinical manifestations include progressive blurred vision, headache, cognitive impairment and generalized tonicclonus in severe cases. 3,8−9 As presented in table1, [10][11][12][13][14][15][16][17][18][19] there were only a few reports on lateral ventricular HB. The case reports by Ho et al, Prieto et al, Jaggi et al and Al-Najar et al were similar to our case in terms of the tumor size, but only the case report by Jaggi et al was very similar to our case, which had no typical clinical symptoms and no VHL-relation.…”

Section: Discussionmentioning

confidence: 99%

A Solitary Hemangioblastoma in the Lateral Ventricle: Case Report and Review of the Literature

Guo

Cao

2022

Preprint

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Background: Hemangioblastoma is a benign tumor occurring in the central nervous system. As known, the most common sites are the cerebellum and spinal cord with the typical appearance which is a nodule with a cyst and contrast-enhanced scan demonstrates the obvious enhancement of the nodule and the local cyst wall. However, it’s difficult to diagnose the hemangioblastoma when it occurs in the lateral ventricle, due to the rare incidence of hemangioblastoma in the lateral ventricle.Case presentation: A 28-year-old man with a 1-month history of recurrent headache accompanied by slight dizziness, then the computed tomography (CT) and magnetic resonance imaging (MRI) of brain showed the cystic solid tumor with obvious enhancement in the parenchymal part and local cystic wall, also, there was abnormal dilated blood vessel in the parenchymal part which was considered as the hemangioblastoma in the lateral ventricle.Conclusions: Total resection of the tumor was performed under neuronavigation, then the tumor was pathologically confirmed to be hemangioblastoma which was the Grade WHOI. Based on this study, we have increased the understanding of hemangioblastoma in the differential diagnosis of tumors located in the lateral ventricle and provide a new method of resection of the tumor.

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“…[ 9 ] To this date, 56 cases of acute hemorrhage have been described with an underlying HGB. [ 1 2 3 5 6 7 10 11 15 16 17 18 20 22 23 24 25 31 33 34 35 37 41 ] A total of 19 cases have been described in the posterior fossa. Large hemorrhages related to HGBs have been described more commonly in spinal locations.…”

Section: Discussionmentioning

confidence: 99%

Recurrent hemorrhage in hemangioblastoma involving the posterior fossa: Case report

Marvin¹,

Akhter²,

Coppens³

2017

Surg Neurol Int

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Background:Hemangioblastomas (HGBs) are the most common primary intra-axial posterior fossa tumor in adults. Although spontaneous hemorrhage of these tumors is exceedingly rare, despite their vascular nature, we describe a case of recurrent hemorrhage with associated tonsillar herniation, and demonstrate that a surgical approach can provide a suitable outcome.Case Description:A 54-year-old female with von Hippel-Lindau (VHL) syndrome presented with acute loss of consciousness and Glasgow Coma Scale (GCS) was 4. Computed tomographic (CT) images demonstrated large volume subarachnoid hemorrhage of the posterior fossa with intraventricular extension and intraparenchymal hemorrhage involving the right cerebellar tonsil. Magnetic resonance imaging (MRI) displayed three lesions in the posterior fossa, two near the hemorrhage site. Patient underwent suboccipital craniectomy with a decent recovery followed by radiosurgery as she refused resection. A second hemorrhage occurred ultimately prompting surgical resection of the three posterior fossa lesions, with a reasonable postoperative course.Conclusion:Hemorrhage of HGBs of the posterior fossa can present in conjunction of tonsillar herniation. Re-hemorrhage appears to be likely if prior acute hemorrhage has occurred. A stepwise approach of surgical decompression and resection may provide the best outcome.

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Sporadic Lateral Ventricular Hemangioblastoma Presenting with Intraventricular and Subarachnoid Haemorrhage = ورم أرومي وعائي فردي في البطين الوحشي ظهر بنزف داخل البطين و نزف تحت العنكبوتية

Cited by 9 publications

References 11 publications

Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature

Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature

A Solitary Hemangioblastoma in the Lateral Ventricle: Case Report and Review of the Literature

Recurrent hemorrhage in hemangioblastoma involving the posterior fossa: Case report

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