Loading…
A primary intraosseous cystic meningioma: Case report
•Intraosseous cystic meningioma is a very rare.•There are no reports of similar cases in the last 30 years.•Primary intraosseous meningioma is a subtype of primary extradural meningioma.•Cystic meningioma is rare, 2–4% of all meningiomas.•A meningioma with both characteristics is an exceptional occu...
Saved in:
Published in: | International journal of surgery case reports 2017-01, Vol.37, p.189-192 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | •Intraosseous cystic meningioma is a very rare.•There are no reports of similar cases in the last 30 years.•Primary intraosseous meningioma is a subtype of primary extradural meningioma.•Cystic meningioma is rare, 2–4% of all meningiomas.•A meningioma with both characteristics is an exceptional occurrence.
This is a very rare case of intraosseous cystic meningioma. There have been no reports of similar cases in the last 30 years.
A 62-year-old man, suffering from a swelling of the lateral wall of the left orbit was admitted to our hospital. MRI and CT scan showed a large intradiploic lesion involving the lateral wall of the orbit and the greater wing of the sphenoid. The lesion was cystic with a mural nodule. We operated the patient and removed completely the mural nodule and the fibrous wall of cyst. Histological examination showed that the mural nodule was a benign meningothelial meningioma.
Primary intraosseous meningiomas represent a subtype of primary extradural meningiomas; they comprise about 2% of all meningiomas and are therefore rare entities. Cystic meningiomas are rare, their incidence compared to all other types of meningiomas is of 2–4%. The presence of a meningioma with both characteristics: cystic and intraosseous, like in our case, is an exceptional occurrence.
The surgical management of tumor was easy; its rarity means that the case is interesting. |
---|---|
ISSN: | 2210-2612 2210-2612 |
DOI: | 10.1016/j.ijscr.2017.06.049 |