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Case Report: A case of primary intracranial parasagittal meningeal angiosarcoma

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Abstract Background Angiosarcoma, also known as malignant hemangioendothelioma, is a rare vasogenic malignant tumor, commonly found on the skin of the head and neck, rarely occurring in the intracranial region.As for intracranial meningeal angiosarcoma, only 7 cases have been reported and there is no clinical study with large sample size. We report here a case of parasagittal meningeal angiosarcoma. Case Description: A 48-year-old Chinese male patient was admitted to our hospital due to headache accompanied by bilateral lower limb weakness. On admission, CT showed a high-density mass on both sides of the sagittal sinus at the top of the frontal lobe. We performed exploratory surgical resection of the tumor. During the operation, it was found that the tumor originated from the dura mater and extensively invaded the surrounding brain tissue and skull, and the surrounding hemosiderin deposition was observed. Postoperative pathology suggested angiosarcoma. Conclusions Intracranial meningeal angiosarcoma is difficult to accurately diagnose before surgery, so radiologists and neurosurgeons need to strengthen their understanding of this disease. The presence of extensive superficial hemosiderin deposition during operation may contribute to the diagnosis, and immunohistochemistry is very important for the diagnosis of intracranial angiosarcoma.
Title: Case Report: A case of primary intracranial parasagittal meningeal angiosarcoma
Description:
Abstract Background Angiosarcoma, also known as malignant hemangioendothelioma, is a rare vasogenic malignant tumor, commonly found on the skin of the head and neck, rarely occurring in the intracranial region.
As for intracranial meningeal angiosarcoma, only 7 cases have been reported and there is no clinical study with large sample size.
We report here a case of parasagittal meningeal angiosarcoma.
Case Description: A 48-year-old Chinese male patient was admitted to our hospital due to headache accompanied by bilateral lower limb weakness.
On admission, CT showed a high-density mass on both sides of the sagittal sinus at the top of the frontal lobe.
We performed exploratory surgical resection of the tumor.
During the operation, it was found that the tumor originated from the dura mater and extensively invaded the surrounding brain tissue and skull, and the surrounding hemosiderin deposition was observed.
Postoperative pathology suggested angiosarcoma.
Conclusions Intracranial meningeal angiosarcoma is difficult to accurately diagnose before surgery, so radiologists and neurosurgeons need to strengthen their understanding of this disease.
The presence of extensive superficial hemosiderin deposition during operation may contribute to the diagnosis, and immunohistochemistry is very important for the diagnosis of intracranial angiosarcoma.

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