Ouadnouni Yassine, Bouchikh Mohammed, Achir Abdellah, Zouaidia Fouad, Smahi Mohammed, Msougar Yassine, Lakranbi Marouane, Afqir Said, Mahassini Najat, Benosman Abdellatif
Department of Thoracic Surgery, Ibn Sina University Hospital, Rabat, Morocco.
Cases J. 2009 Sep 3;2:8235. doi: 10.4076/1757-1626-2-8235.
The pulmonary epithelioid hemangioendothelioma is a rare vascular intermediate malignancy tumour.
A 45-year-old man, he shows an isolated chronic cough with a preserved general state of health. The thoracoabdominal Computed tomography showed three well limited opacities of the right lung, among them one shows some calcifications; which we entirely resected by enucleation after a pneumotomy. The histologic examination with immunomarking led to an epithelioid hemangioendothelioma.
The pulmonary epithelioid hemangioendothelioma is a tumour of unpredictable prognosis, bad when linked to the plurifocal and symptomatic forms.
肺上皮样血管内皮瘤是一种罕见的血管中间型恶性肿瘤。
一名45岁男性,表现为单纯慢性咳嗽,全身健康状况良好。胸腹部计算机断层扫描显示右肺有三个边界清晰的不透明区,其中一个有一些钙化;我们在开胸术后通过摘除术将其完全切除。免疫标记的组织学检查结果为上皮样血管内皮瘤。
肺上皮样血管内皮瘤是一种预后不可预测的肿瘤,与多灶性和有症状的形式相关时预后较差。