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The efficacy and safety of an oral iron chelating agent, deferasirox, for iron overload in a patient with chronic kidney disease and myelodysplastic syndrome
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- Fukui Shinji
- Department of Urology, Nara Prefectural Nara Hospital
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- Torimoto Kazumasa
- Department of Urology, Nara Prefectural Nara Hospital
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- Kagebayashi Yoriaki
- Department of Urology, Nara Prefectural Nara Hospital
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- Morimoto Katsuhiko
- Department of Cardiology and Nephrology, Nara Prefectural Nara Hospital
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- Yamaguchi Soichi
- Department of Cardiology and Nephrology, Nara Prefectural Nara Hospital
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- Hamano Kazumasa
- Department of Cardiology and Nephrology, Nara Prefectural Nara Hospital
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- Samma Shoji
- Department of Urology, Nara Prefectural Nara Hospital
Bibliographic Information
- Other Title
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- 慢性腎不全・骨髄異形成症候群合併症例における鉄過剰症に対する経口鉄キレート剤の効果と安全性
- マンセイ ジンフゼン コツズイイケイセイ ショウコウグン ガッペイ ショウレイ ニ オケル テツ カジョウショウ ニ タイスル ケイコウテツ キレートザイ ノ コウカ ト アンゼンセイ
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Description
A 76-year-old man was introduced to maintenance hemodialysis in February 2006 due to gradually progressed renal failure following right nephrectomy for kidney cancer in 1995. The patient was referred to our department in May 2008 because of a right adrenal tumor associated with erythropoietin-resistant anemia. The adrenal tumor was probably a metastasis from kidney cancer. On magnetic resonance imaging, the liver showed a markedly low intensity on T2-weighted images, suggesting hemochromatosis. In addition, a serum level of ferritin was markedly elevated at 2,314 ng/mL. Iron overload might have been due to excessive intravenous iron administration as well as frequent blood transfusion. Following extirpation of the adrenal tumor, bone marrow biopsy was performed. The patient was diagnosed as having myelodysplastic syndrome : ringed sideroblasts comprised 20% of sideroblasts. Considering the physical condition of the patient, periodic blood transfusion was performed to treat anemia. Simultaneously, iron overload was treated with an oral chelating agent, deferasirox, starting in June 2008. The dose of deferasirox was gradually increased from 500 mg daily to the maximum dose of 1,250 mg daily while monitoring serum ferritin levels. Then, the dose was reduced when the serum ferritin level became less than 1,000 ng/mL. The only adverse event of deferasirox was diarrhea, which was well controlled with oral medication. In February 2009, after 9 months of deferasirox administration, the serum ferritin level was 467 ng/mL. Subsequently, administration of deferasirox was ceased. This is the first report in Japan of deferasirox administration to a dialytic patient. This agent would be one of the treatment options for iron overload even in hemodialysis patients.
Journal
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- Nihon Toseki Igakkai Zasshi
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Nihon Toseki Igakkai Zasshi 42 (11), 865-869, 2009
The Japanese Society for Dialysis Therapy
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Keywords
Details 詳細情報について
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- CRID
- 1390001204679984000
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- NII Article ID
- 10026315800
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- NII Book ID
- AN10432053
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- ISSN
- 1883082X
- 13403451
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- NDL BIB ID
- 10512190
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL Search
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed