Benzylthiouracil-Induced Glomerulonephritis

Vasculitis is a rare complication of antithyroid drugs (ATDs). It was first described with Propylthiouracil (PTU). We report a new case of antineutrophil cytoplasmic antibody (ANCA) vasculitis with glomerulonephritis induced by Benzylthiouracile (BTU). A 50-year-old man with Graves disease treated w...

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Main Authors: Sihem Trimeche Ajmi, Rim Braham, Sarra Toumi, Molka Chadli Chaieb, Amel Maaroufi, Koussay Ach, Larbi Chaieb
Format: Article
Language:English
Published: Wiley 2009-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2009/687285
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author Sihem Trimeche Ajmi
Rim Braham
Sarra Toumi
Molka Chadli Chaieb
Amel Maaroufi
Koussay Ach
Larbi Chaieb
author_facet Sihem Trimeche Ajmi
Rim Braham
Sarra Toumi
Molka Chadli Chaieb
Amel Maaroufi
Koussay Ach
Larbi Chaieb
author_sort Sihem Trimeche Ajmi
collection DOAJ
description Vasculitis is a rare complication of antithyroid drugs (ATDs). It was first described with Propylthiouracil (PTU). We report a new case of antineutrophil cytoplasmic antibody (ANCA) vasculitis with glomerulonephritis induced by Benzylthiouracile (BTU). A 50-year-old man with Graves disease treated with BTU developed general malaise and haematuria without skin rash or respiratory involvement. Laboratory data revealed acute renal failure with proteinuria and haematuria. An indirect immunofluorescence test for ANCA was positive, showing a perinuclear pattern with specificity antimyeloperoxidase (MPO). A renal biopsy was performed and revealed pauci-immune extracapillary glomerular nephropathy and necrotic vasculitis lesions. Based on these findings we concluded to the diagnosis of rapidly progressive glomerulonephritis associated with ANCA induced by BTU therapy. The drug was therefore discontinued and the patient was treated with steroids and immunosuppressive treatment during 3 months. Renal failure, proteinuria and haematuria significantly improved within 2 months. However, P-ANCA remained positive until 10 months after drug withdrawal. Thyroid function was kept within normal range using iodine solution. We demonstrated clearly that BTU may induce severe forms of vasculitis with glomerulonephritis. Thus, the ANCA must be measured when confronted to systemic manifestation during treatment.
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spelling doaj-art-c5d9c7aeb8a74e4aaa723f15e303f7522025-02-03T01:10:45ZengWileyCase Reports in Medicine1687-96271687-96352009-01-01200910.1155/2009/687285687285Benzylthiouracil-Induced GlomerulonephritisSihem Trimeche Ajmi0Rim Braham1Sarra Toumi2Molka Chadli Chaieb3Amel Maaroufi4Koussay Ach5Larbi Chaieb6Department of Endocrinology, Farhat Hached Hospital, 4000 Sousse, TunisiaDepartment of Endocrinology, Farhat Hached Hospital, 4000 Sousse, TunisiaDepartment of Internal Medicine, Sahloul Hospital, Sousse, TunisiaDepartment of Endocrinology, Farhat Hached Hospital, 4000 Sousse, TunisiaDepartment of Endocrinology, Farhat Hached Hospital, 4000 Sousse, TunisiaDepartment of Endocrinology, Farhat Hached Hospital, 4000 Sousse, TunisiaDepartment of Endocrinology, Farhat Hached Hospital, 4000 Sousse, TunisiaVasculitis is a rare complication of antithyroid drugs (ATDs). It was first described with Propylthiouracil (PTU). We report a new case of antineutrophil cytoplasmic antibody (ANCA) vasculitis with glomerulonephritis induced by Benzylthiouracile (BTU). A 50-year-old man with Graves disease treated with BTU developed general malaise and haematuria without skin rash or respiratory involvement. Laboratory data revealed acute renal failure with proteinuria and haematuria. An indirect immunofluorescence test for ANCA was positive, showing a perinuclear pattern with specificity antimyeloperoxidase (MPO). A renal biopsy was performed and revealed pauci-immune extracapillary glomerular nephropathy and necrotic vasculitis lesions. Based on these findings we concluded to the diagnosis of rapidly progressive glomerulonephritis associated with ANCA induced by BTU therapy. The drug was therefore discontinued and the patient was treated with steroids and immunosuppressive treatment during 3 months. Renal failure, proteinuria and haematuria significantly improved within 2 months. However, P-ANCA remained positive until 10 months after drug withdrawal. Thyroid function was kept within normal range using iodine solution. We demonstrated clearly that BTU may induce severe forms of vasculitis with glomerulonephritis. Thus, the ANCA must be measured when confronted to systemic manifestation during treatment.http://dx.doi.org/10.1155/2009/687285
spellingShingle Sihem Trimeche Ajmi
Rim Braham
Sarra Toumi
Molka Chadli Chaieb
Amel Maaroufi
Koussay Ach
Larbi Chaieb
Benzylthiouracil-Induced Glomerulonephritis
Case Reports in Medicine
title Benzylthiouracil-Induced Glomerulonephritis
title_full Benzylthiouracil-Induced Glomerulonephritis
title_fullStr Benzylthiouracil-Induced Glomerulonephritis
title_full_unstemmed Benzylthiouracil-Induced Glomerulonephritis
title_short Benzylthiouracil-Induced Glomerulonephritis
title_sort benzylthiouracil induced glomerulonephritis
url http://dx.doi.org/10.1155/2009/687285
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AT koussayach benzylthiouracilinducedglomerulonephritis
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