Intradiploic cavernous hemangioma presenting as multiple craters on skull

Ramdasi, Raghvendra; Mahore, Amit; Thorve, Smita; Patil, Manoj

doi:10.1007/s00701-016-2752-1

Cited by 2 publications

(10 citation statements)

References 6 publications

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“…CH in cranial vault, are slow-growing lesions and typically occur in women in the second through fourth decades. Only less than 10% of cases are observed during the first decade as in our cases [1][2][3]5,6,[8][9][10] . The natural history of untreated lesions is poorly described.…”

Section: Discussioncontrasting

confidence: 49%

“…Overall, they represent less than 1% of all osseous benign tumors [1][2][3]5,6,[8][9][10] . The parietal bone is thought to be the most commonly affected, followed by the frontal bone and less frequently by occipital and temporal bones.…”

Section: Discussionmentioning

confidence: 99%

“…The natural history of untreated lesions is poorly described. Cosmetic alterations, bleeding, and cranial nerves with progressive involvement in tumors of the skull base, as well as progressive exophthalmia and impairment of ocular movements in orbital lesions, were reported in some cases 1,2,[5][6][7][8][9][10] . The symptoms are usually pain and visible or palpable bony hard mass or skull defect, slowly growing, covered by normal skin.…”

Section: Discussionmentioning

confidence: 99%

“…High signal intensity on T2-weighted MRI may be caused by pooling of blood or slow-flowing blood. In angiographic examination, most of CH lacks a vascular blush, and diagnosis of hemangioma may not be suggested [1][2][3][4][5][6][8][9][10] . CH are composed of group of large, dilated blood vessels separated by fibrous tissue, whereas capillary hemangiomas lack fibrous septa and have smaller vascular lumens.…”

Section: Discussionmentioning

confidence: 99%

“…Primary cavernous hemangiomas (CH) in cranial vault were uncommon and rare tumor, accounting for less than 1.0% of all bone neoplasms. These tumors are mostly found in vertebral bodies [1][2][3]5,6,[8][9][10] . We report a case of CH in parietal cranial vault and successfully managed with surgical resection.…”

Section: Introductionmentioning

confidence: 99%

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Cavernous Hemangioma in Cranial Vault: A Case Report

Park

Hwang

2020

Nerve

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Cavernous hemangioma (CH) in cranial vault is rare comprising about less than 1% of all benign neoplasms of the bone. The vertebral column is most often affected, followed by the cranial vault. We describe a case of CH in parietal cranial vault. A 6-year-old child presented with skull depression. Brain computed tomography scan revealed a bone defect due to extrinsic compression by soft tissue mass at right parietal bone. This lesion was not without intracranial extension or associated brain abnormality. Brain magnetic resonance image showed a lesion of signal abnormality with low signal intensity on T1 image and high signal intensity on T2-weighted images with no enhancement. She was treated by operation with total excision of mass followed by a cranioplasty. Pathologic examination revealed a capillary hemangioma consisting of thin-walled blood vessels, some of which were distended with blood. She recovered to a favorable state without any neurological deficit.

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Section: Discussioncontrasting

confidence: 49%

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

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Cavernous Hemangioma in Cranial Vault: A Case Report

Park

Hwang

2020

Nerve

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Case report: Cavernous hemangioma in the right frontoparietal junction

et al. 2022

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BackgroundPrimary intraosseous cavernous hemangioma is a benign tumor with slow growth and is rarely seen in clinics. The clinical manifestations of most patients are progressive enlargement of the head mass.Case presentationWe report a 30-year-old female patient with cavernous hemangioma at the frontoparietal junction. Upon admission, the right frontal lobe mass was progressively enlarged for 3 years and underwent lesion resection and stage I skull reconstruction. The postoperative outcome was good, with no recurrence at 1-year follow-up.ConclusionPrimary intraosseous cavernous hemangioma is a relatively rare clinical tumor, the pathogenesis of which is still unclear, and most of them have no specific clinical manifestations. Characteristic imaging findings are highly suspicious of this disease, but the definitive diagnosis still depends on histopathological examination. Currently, total surgical resection of the tumor is a relatively effective and preferred treatment.

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Intradiploic cavernous hemangioma presenting as multiple craters on skull

Cited by 2 publications

References 6 publications

Cavernous Hemangioma in Cranial Vault: A Case Report

Cavernous Hemangioma in Cranial Vault: A Case Report

Case report: Cavernous hemangioma in the right frontoparietal junction

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