Primer Adrenal Schwannom : A Rare Case
Solitary-cystic Schwannoma arising from adrenal gland is seen extremely rare. Its frequency in our country is unknown. Schwannomas are responsible for 1-5% of all retroperitoneal masses and c...
| Format: | Article |
|---|---|
| Language: | English |
| Published: |
Mustafa Kemal University
2016-12-01
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| Series: | Mustafa Kemal Üniversitesi Tıp Dergisi |
| Subjects: | |
| Online Access: | http://dergipark.gov.tr/mkutfd/issue/19607/209571?publisher=mku |
| _version_ | 1797917954492334080 |
|---|---|
| collection | DOAJ |
| description | Solitary-cystic Schwannoma arising from adrenal gland
is seen extremely rare. Its frequency in
our country is unknown. Schwannomas are responsible for 1-5% of all
retroperitoneal masses and clinical signs are non-specific. They are diagnosed
incidentally as in our case and generally their first sign is referred pain. CT
and MR are important screening methods. However, the final diagnosis is made by
pathological examination. The prognosis is excellent after total resection. It
is valuable to present the primary adrenal schwannoma arising from adrenal
gland because of its rare incidence in all of the world thus this is the first case in our country. |
| first_indexed | 2024-04-10T13:21:40Z |
| format | Article |
| id | doaj.art-ae06ccb6cd84420ca5d3645f5b591883 |
| institution | Directory Open Access Journal |
| issn | 2149-3103 |
| language | English |
| last_indexed | 2024-04-10T13:21:40Z |
| publishDate | 2016-12-01 |
| publisher | Mustafa Kemal University |
| record_format | Article |
| series | Mustafa Kemal Üniversitesi Tıp Dergisi |
| spelling | doaj.art-ae06ccb6cd84420ca5d3645f5b5918832023-02-15T16:12:01ZengMustafa Kemal UniversityMustafa Kemal Üniversitesi Tıp Dergisi2149-31032016-12-01728565910.17944/mkutfd.209571102Primer Adrenal Schwannom : A Rare CaseSolitary-cystic Schwannoma arising from adrenal gland is seen extremely rare. Its frequency in our country is unknown. Schwannomas are responsible for 1-5% of all retroperitoneal masses and clinical signs are non-specific. They are diagnosed incidentally as in our case and generally their first sign is referred pain. CT and MR are important screening methods. However, the final diagnosis is made by pathological examination. The prognosis is excellent after total resection. It is valuable to present the primary adrenal schwannoma arising from adrenal gland because of its rare incidence in all of the world thus this is the first case in our country.http://dergipark.gov.tr/mkutfd/issue/19607/209571?publisher=mku-Adrenal bezschwann hücrelerineoplazmAdrenal glandschwann cellsneoplasm |
| spellingShingle | Primer Adrenal Schwannom : A Rare Case Mustafa Kemal Üniversitesi Tıp Dergisi - Adrenal bez schwann hücreleri neoplazm Adrenal gland schwann cells neoplasm |
| title | Primer Adrenal Schwannom : A Rare Case |
| title_full | Primer Adrenal Schwannom : A Rare Case |
| title_fullStr | Primer Adrenal Schwannom : A Rare Case |
| title_full_unstemmed | Primer Adrenal Schwannom : A Rare Case |
| title_short | Primer Adrenal Schwannom : A Rare Case |
| title_sort | primer adrenal schwannom a rare case |
| topic | - Adrenal bez schwann hücreleri neoplazm Adrenal gland schwann cells neoplasm |
| url | http://dergipark.gov.tr/mkutfd/issue/19607/209571?publisher=mku |