Pekcolaklar A, Turna A, Urer N, Gürses A
Department of Thoracic Surgery, Yedikule Teaching Hospital for Chest Diseases and Thoracic Surgery, Istanbul, Turkey.
Acta Chir Belg. 2007 Jun;107(3):328-30. doi: 10.1080/00015458.2007.11680068.
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.
我们报告了一例影像学表现为囊性病变的肺硬化性血管瘤病例。发现该患者有特异性抗棘球蚴免疫球蛋白E，因此术前诊断为肺包虫囊肿。进行了手术切除。肺硬化性血管瘤虽然罕见，但在影像学和血清学上可能与肺包虫囊肿相似。这两种情况都需要在不进行实质切除的情况下完整切除病变。
