A Case of Thrombotic Microangiopathy, Podocytopathy, and Damage to the Renal Tubules with Severe Proteinuria and Acute Renal Dysfunction Induced by Lenvatinib
Lenvatinib, a tyrosine kinase inhibitor (TKI), is a stronger inhibitor of vascular endothelial growth factor receptor, fibroblast growth factor receptors 1 to 4, and platelet-derived growth factor receptor (PDGFR) than other TKIs. We herein report a 77-year-old Japanese woman who received the minimu...
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Veröffentlicht in: | Internal Medicine 2022, pp.8365-21 |
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creator | Nakashima, Saki Sekine, Akinari Sawa, Naoki Kawamura, Yusuke Kono, Kei Kinowaki, Keiichi Kawada, Masahiro Hasegawa, Eiko Akuta, Norio Suzuki, Yoshiyuki Ohashi, Kenichi Takaichi, Kenmei Ubara, Yoshifumi Hoshino, Junichi |
description | Lenvatinib, a tyrosine kinase inhibitor (TKI), is a stronger inhibitor of vascular endothelial growth factor receptor, fibroblast growth factor receptors 1 to 4, and platelet-derived growth factor receptor (PDGFR) than other TKIs. We herein report a 77-year-old Japanese woman who received the minimum dose of lenvatinib for treatment of hepatocellular carcinoma. Within one month of starting treatment, she developed severe proteinuria, hypertension, and renal dysfunction. A kidney biopsy showed drug-induced thrombotic microangiopathy, podocytopathy, and polar vasculosis. We also observed damage to the renal tubules, where PDGFR is located. To our knowledge, this is the first report of lenvatinib-induced damage to the renal tubules. |
doi_str_mv | 10.2169/internalmedicine.8365-21 |
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Med.</addtitle><date>2022-03-26</date><risdate>2022</risdate><spage>8365-21</spage><pages>8365-21-</pages><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>Lenvatinib, a tyrosine kinase inhibitor (TKI), is a stronger inhibitor of vascular endothelial growth factor receptor, fibroblast growth factor receptors 1 to 4, and platelet-derived growth factor receptor (PDGFR) than other TKIs. We herein report a 77-year-old Japanese woman who received the minimum dose of lenvatinib for treatment of hepatocellular carcinoma. Within one month of starting treatment, she developed severe proteinuria, hypertension, and renal dysfunction. A kidney biopsy showed drug-induced thrombotic microangiopathy, podocytopathy, and polar vasculosis. We also observed damage to the renal tubules, where PDGFR is located. To our knowledge, this is the first report of lenvatinib-induced damage to the renal tubules.</abstract><cop>Japan</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>35342129</pmid><doi>10.2169/internalmedicine.8365-21</doi><oa>free_for_read</oa></addata></record> |
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subjects | damage to the renal tubules lenvatinib podocytopathy thrombotic microangiopathy |
title | A Case of Thrombotic Microangiopathy, Podocytopathy, and Damage to the Renal Tubules with Severe Proteinuria and Acute Renal Dysfunction Induced by Lenvatinib |
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