| dc.contributor.author | Uerer, N. | |
| dc.contributor.author | Turna, A. | |
| dc.contributor.author | Guerses, A. | |
| dc.contributor.author | Pekcolaklar, A. | |
| dc.date.accessioned | 2021-03-03T09:44:09Z | |
| dc.date.available | 2021-03-03T09:44:09Z | |
| dc.date.issued | 2007 | |
| dc.identifier.citation | Pekcolaklar A., Turna A., Uerer N., Guerses A., "Pulmonary sclerosing haemangioma mimicking hydatid cyst: a case report", ACTA CHIRURGICA BELGICA, cilt.107, sa.3, ss.328-330, 2007 | |
| dc.identifier.issn | 0001-5458 | |
| dc.identifier.other | av_1e96ca53-0c1f-44c9-ad8f-54c528f42a3a | |
| dc.identifier.other | vv_1032021 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12627/25711 | |
| dc.identifier.uri | https://doi.org/10.1080/00015458.2007.11680068 | |
| dc.description.abstract | We report the case of a pulmonary sclerosing haemangioma radiologically presenting as a cystic lesion. The patient was found to have specific anti-echinococcus immunoglobulin E and therefore the preoperative diagnosis was that of pulmonary hydatid cyst. A surgical resection was performed. Although rarely encountered, pulmonary sclerosing haemangioma may show radiological and serological similarities to a pulmonary hydatid cyst. Both entities necessitate complete removal of the lesion without parenchymal resection. | |
| dc.language.iso | eng | |
| dc.subject | Klinik Tıp (MED) | |
| dc.subject | Sağlık Bilimleri | |
| dc.subject | CERRAHİ | |
| dc.subject | Klinik Tıp | |
| dc.subject | Tıp | |
| dc.subject | Cerrahi Tıp Bilimleri | |
| dc.title | Pulmonary sclerosing haemangioma mimicking hydatid cyst: a case report | |
| dc.type | Makale | |
| dc.relation.journal | ACTA CHIRURGICA BELGICA | |
| dc.contributor.department | , , | |
| dc.identifier.volume | 107 | |
| dc.identifier.issue | 3 | |
| dc.identifier.startpage | 328 | |
| dc.identifier.endpage | 330 | |
| dc.contributor.firstauthorID | 727235 | |
