Abstract
Pulmonary epithelioid hemangioendothelioma (PEH) is a rare vascular tumor of borderline or low-grade malignancy, Vascular endothelial growth factor (VEGF) and the VEGF receptor were found on PEH tumor cells, suggesting that target therapies that block VEGFR have a logical base in this rare malignancy. We report a 25 years old woman with a pulmonary hemangioendothelioma, treated with pazopanib, the only anti angiogenic registered agent for sarcoma, with clinical improvement of symptoms and durable stabilization for more than two years of lung tumor.
Keywords:
morocco, Hemangioendothelioma
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How to Cite
Ahalli, I., Oualla, K., Hejjane, L., Boujarnija, R., Messoudi, K., Mai, A., … Mellas, N. (2020). Pazopanib in Pulmonary Epithelioid Hemangioendothelioma: Report of a Case. International Journal of Innovative Research in Medical Science, 5(02), 84 to 87. https://doi.org/10.23958/ijirms/vol05-i02/828
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Copyright © 2020 Ibtihal Ahalli Karima Oualla Loubna Hejjane Raihana Boujarnija Kaouthar Messoudi Adil Mai Fatima Zahrae Er Reggad Lamiaa Amaadour Zineb Benbrahim Samia Arifi Badr Alami Laila Chbani Nawfel Mellas this is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
This work is licensed under a Creative Commons Attribution 4.0 International License.
