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A case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis

Only a few cases of renal vein thrombosis (RVT) occurring in patients with vasculitis have been reported. RVT associated with vasculitis and hemolytic anemia has not been reported yet. We describe here a patient with RVT complicated by pulmonary embolism, autoimmune hemolytic anemia, and eosinophili...

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Autores principales: Watanabe, Yusaku, Hirai, Keiji, Matsuyama, Momoko, Kitano, Taisuke, Ito, Kiyonori, Kobashigawa, Tsuyoshi, Ookawara, Susumu, Morishita, Yoshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683572/
https://www.ncbi.nlm.nih.gov/pubmed/37756584
http://dx.doi.org/10.1177/03000605231200272
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author Watanabe, Yusaku
Hirai, Keiji
Matsuyama, Momoko
Kitano, Taisuke
Ito, Kiyonori
Kobashigawa, Tsuyoshi
Ookawara, Susumu
Morishita, Yoshiyuki
author_facet Watanabe, Yusaku
Hirai, Keiji
Matsuyama, Momoko
Kitano, Taisuke
Ito, Kiyonori
Kobashigawa, Tsuyoshi
Ookawara, Susumu
Morishita, Yoshiyuki
author_sort Watanabe, Yusaku
collection PubMed
description Only a few cases of renal vein thrombosis (RVT) occurring in patients with vasculitis have been reported. RVT associated with vasculitis and hemolytic anemia has not been reported yet. We describe here a patient with RVT complicated by pulmonary embolism, autoimmune hemolytic anemia, and eosinophilic granulomatous polyangiitis. A 69-year-old Japanese man who had been treated with corticosteroids was referred to our department for severe proteinuria (4.32 g/gCr). Abdominal ultrasonography showed bilateral RVT, and contrast-enhanced computed tomography showed bilateral pulmonary embolism. Therefore, the patient was diagnosed with RVT complicated by pulmonary embolism. Anticoagulation therapy with heparin followed by apixaban was started. Thereafter, the D-dimer concentration decreased from 8.3 to 1.2 μg/mL, and urinary protein excretion improved to 0.62 g/gCr. Renal function was unchanged with an estimated glomerular filtration rate of 68.8 mL/minute/1.73 m(2). The thrombi in both renal veins and pulmonary arteries gradually regressed. Clinicians should be aware of this complication when worsening proteinuria is observed during steroid therapy in patients with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis.
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spelling pubmed-106835722023-11-30 A case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis Watanabe, Yusaku Hirai, Keiji Matsuyama, Momoko Kitano, Taisuke Ito, Kiyonori Kobashigawa, Tsuyoshi Ookawara, Susumu Morishita, Yoshiyuki J Int Med Res Case Report Only a few cases of renal vein thrombosis (RVT) occurring in patients with vasculitis have been reported. RVT associated with vasculitis and hemolytic anemia has not been reported yet. We describe here a patient with RVT complicated by pulmonary embolism, autoimmune hemolytic anemia, and eosinophilic granulomatous polyangiitis. A 69-year-old Japanese man who had been treated with corticosteroids was referred to our department for severe proteinuria (4.32 g/gCr). Abdominal ultrasonography showed bilateral RVT, and contrast-enhanced computed tomography showed bilateral pulmonary embolism. Therefore, the patient was diagnosed with RVT complicated by pulmonary embolism. Anticoagulation therapy with heparin followed by apixaban was started. Thereafter, the D-dimer concentration decreased from 8.3 to 1.2 μg/mL, and urinary protein excretion improved to 0.62 g/gCr. Renal function was unchanged with an estimated glomerular filtration rate of 68.8 mL/minute/1.73 m(2). The thrombi in both renal veins and pulmonary arteries gradually regressed. Clinicians should be aware of this complication when worsening proteinuria is observed during steroid therapy in patients with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis. SAGE Publications 2023-09-27 /pmc/articles/PMC10683572/ /pubmed/37756584 http://dx.doi.org/10.1177/03000605231200272 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Watanabe, Yusaku
Hirai, Keiji
Matsuyama, Momoko
Kitano, Taisuke
Ito, Kiyonori
Kobashigawa, Tsuyoshi
Ookawara, Susumu
Morishita, Yoshiyuki
A case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis
title A case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis
title_full A case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis
title_fullStr A case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis
title_full_unstemmed A case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis
title_short A case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis
title_sort case of renal vein thrombosis associated with autoimmune hemolytic anemia and eosinophilic granulomatous polyangiitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683572/
https://www.ncbi.nlm.nih.gov/pubmed/37756584
http://dx.doi.org/10.1177/03000605231200272
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