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Malignant hepatic vascular tumors in adults: Characteristics,diagnostic difficulties and current management 被引量:10
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作者 Daniela Cornelia Lazar Mihaela Flavia Avram +3 位作者 Ioan Romosan Violetta Vacariu Adrian Goldis Marioara Cornianu 《World Journal of Clinical Oncology》 2019年第3期110-135,共26页
Malignant vascular tumors of the liver include rare primary hepatic mesenchymal tumors developed in the background of a normal liver parenchyma. Most of them are detected incidentally by the increased use of performin... Malignant vascular tumors of the liver include rare primary hepatic mesenchymal tumors developed in the background of a normal liver parenchyma. Most of them are detected incidentally by the increased use of performing imaging techniques. Their diagnosis is challenging, involving clinical and imaging criteria, with final confirmation by histology and immunohistochemistry. Surgery represents the mainstay of treatment. Liver transplantation(LT) has improved substantially the prognosis of hepatic epithelioid hemangioendothelioma(HEHE), with 5-year patient survival rates of up to 81%, based on the European Liver Intestine Transplantation AssociationEuropean Liver Transplant Registry study. Unfortunately, the results of surgery and LT are dismal in cases of hepatic angiosarcoma(HAS). Due to the disappointing results of very short survival periods of approximately 6-7 mo after LT, because of tumor recurrence and rapid progression of the disease, HAS is considered an absolute contraindication to LT. Recurrences after surgical resection are high in cases of HEHE and invariably present in cases of HAS. The discovery of reliable prognostic markers and the elaboration of prognostic scores following LT are needed to provide the best therapeutic choice for each patient.Studies on a few patients have demonstrated the stabilization of the disease in a proportion of patients with hepatic vascular tumors using novel targeted antiangiogenic agents, cytokines or immunotherapy. These new approaches,alone or in combination with other therapeutic modalities, such as surgery and classical chemotherapy, need further investigation to assess their role in prolonging patient survival. Personalized therapeutic algorithms according to the histopathological features, behavior, molecular biology and genetics of the tumors should be elaborated in the near future for the management of patients diagnosed with primary malignant vascular tumors of the liver. 展开更多
关键词 Hepatic malignant vascular tumors Hepatic small vessel neoplasia Hepaticperivascular epithelioid cell tumor Hepatic hemangiopericytoma Hepatic epithelioidhemangioendothelioma Kaposi sarcoma Hepatic angiosarcoma DIAGNOSTIC Prognostic Treatment
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肺上皮样血管内皮瘤的诊治进展 被引量:5
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作者 薛志红(综述) 何朗(审校) 《肿瘤预防与治疗》 2020年第3期262-268,共7页
上皮样血管内皮瘤属于血管源性肿瘤,起源于血管内皮,可发生于身体多个部位,以肝脏、骨骼和肺为主。而原发于肺的上皮样血管内皮瘤(pulmonary epithelioid hemangioendothelioma,P-EHE)是罕见的中低度恶性肿瘤,大多以散发病例报道为主,... 上皮样血管内皮瘤属于血管源性肿瘤,起源于血管内皮,可发生于身体多个部位,以肝脏、骨骼和肺为主。而原发于肺的上皮样血管内皮瘤(pulmonary epithelioid hemangioendothelioma,P-EHE)是罕见的中低度恶性肿瘤,大多以散发病例报道为主,缺乏流行病学调查。因P-EHE发病率低、临床症状及影像学表现缺乏特异性,易误诊、漏诊,导致患者接受不适当治疗及预后不良。其诊断依据是基于独特的组织学、免疫组化及分子特征。因P-EHE较为少见,目前尚无标准有效治疗措施,手术适用于病灶较少的病例,放疗在骨转移病灶及病灶局控上显示较好疗效,抗血管生成的靶向治疗显示较好的应用前景。P-EHE异质性较强,预后介于良性及高度恶性肿瘤之间。本文对该病的发病机制、诊断、临床特征、治疗及预后的研究进展进行综述。 展开更多
关键词 上皮样血管内皮瘤 肺上皮样血管内皮瘤 发病机制 诊断 治疗 预后
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