| dc.contributor.author | GUNES, HA | |
| dc.contributor.author | EGILMEZ, R | |
| dc.contributor.author | DULGER, M | |
| dc.date.accessioned | 2019-07-27T12:10:23Z | |
| dc.date.accessioned | 2019-07-28T10:38:57Z | |
| dc.date.available | 2019-07-27T12:10:23Z | |
| dc.date.available | 2019-07-28T10:38:57Z | |
| dc.date.issued | 1990 | |
| dc.identifier.issn | 0007-0947 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12418/11992 | |
| dc.description | WOS: A1990FM70000093 | en_US |
| dc.description | PubMed ID: 2102218 | en_US |
| dc.description.abstract | Although ovaries have a very rich vasculature, haemangiomas of the ovary are extremely rare. There are only another 39 cases of ovarian haemangioma recorded in the literature. We describe an 11-year-old girl with an ovarian haemangioma who presented clinically with an acute abdomen. The patient has been well without complications for a year. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | MEDICOM INTERNATIONAL | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | OVARIAN HEMANGIOMA | en_US |
| dc.type | article | en_US |
| dc.relation.journal | BRITISH JOURNAL OF CLINICAL PRACTICE | en_US |
| dc.identifier.volume | 44 | en_US |
| dc.identifier.issue | 12 | en_US |
| dc.identifier.endpage | 735 | en_US |
| dc.identifier.startpage | 734 | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
