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Simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis
Granulomatosis with polyangiitis (GPA) is a systemic necrotizing granulomatous vasculitis, which predominantly affects small‐sized blood vessels. We aimed to report a case of GPA involving testicles and epididymis taken for malignancy. A 75‐year‐old patient was admitted for a painful left testicular...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361717/ https://www.ncbi.nlm.nih.gov/pubmed/35957766 http://dx.doi.org/10.1002/ccr3.6231 |
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author | Kechida, Melek Ktari, Kamel Jellazi, Mohamed Mesfar, Rym Khochtali, Ines Saad, Hammadi Njim, Leila |
author_facet | Kechida, Melek Ktari, Kamel Jellazi, Mohamed Mesfar, Rym Khochtali, Ines Saad, Hammadi Njim, Leila |
author_sort | Kechida, Melek |
collection | PubMed |
description | Granulomatosis with polyangiitis (GPA) is a systemic necrotizing granulomatous vasculitis, which predominantly affects small‐sized blood vessels. We aimed to report a case of GPA involving testicles and epididymis taken for malignancy. A 75‐year‐old patient was admitted for a painful left testicular mass. There was no extra urogenital manifestations on examination and the workup was unremarkable. Histological findings after orchidectomy revealed granulomatous inflammation of the testis and epididymis with fibrinoid necrosis and necrotic vasculitis consisting with the diagnosis of GPA. Further investigations regarding ear, nose, throat, pulmonary, and renal involvement were negative. Proteinase 3 antineutrophil cytoplasmic antibodies (PR3‐ANCA) test was negative. Furthermore, infectious diseases especially tuberculosis were ruled out. Based on histopathological findings, limited GPA was diagnosed. The patient was treated with methotrexate and prednisone with good outcome. There was no relapse after 1 year of follow‐up. Isolated urogenital involvement may occur at the onset of GPA and can be taken for malignancy. Histopathological findings are the gold standard for the diagnosis. Treatment is based on steroids and immunosuppressive drugs. |
format | Online Article Text |
id | pubmed-9361717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93617172022-08-10 Simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis Kechida, Melek Ktari, Kamel Jellazi, Mohamed Mesfar, Rym Khochtali, Ines Saad, Hammadi Njim, Leila Clin Case Rep Case Report Granulomatosis with polyangiitis (GPA) is a systemic necrotizing granulomatous vasculitis, which predominantly affects small‐sized blood vessels. We aimed to report a case of GPA involving testicles and epididymis taken for malignancy. A 75‐year‐old patient was admitted for a painful left testicular mass. There was no extra urogenital manifestations on examination and the workup was unremarkable. Histological findings after orchidectomy revealed granulomatous inflammation of the testis and epididymis with fibrinoid necrosis and necrotic vasculitis consisting with the diagnosis of GPA. Further investigations regarding ear, nose, throat, pulmonary, and renal involvement were negative. Proteinase 3 antineutrophil cytoplasmic antibodies (PR3‐ANCA) test was negative. Furthermore, infectious diseases especially tuberculosis were ruled out. Based on histopathological findings, limited GPA was diagnosed. The patient was treated with methotrexate and prednisone with good outcome. There was no relapse after 1 year of follow‐up. Isolated urogenital involvement may occur at the onset of GPA and can be taken for malignancy. Histopathological findings are the gold standard for the diagnosis. Treatment is based on steroids and immunosuppressive drugs. John Wiley and Sons Inc. 2022-08-09 /pmc/articles/PMC9361717/ /pubmed/35957766 http://dx.doi.org/10.1002/ccr3.6231 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Kechida, Melek Ktari, Kamel Jellazi, Mohamed Mesfar, Rym Khochtali, Ines Saad, Hammadi Njim, Leila Simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis |
title | Simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis |
title_full | Simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis |
title_fullStr | Simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis |
title_full_unstemmed | Simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis |
title_short | Simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis |
title_sort | simultaneous testicle and epididymis vasculitis revealing granulomatosis with polyangiitis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361717/ https://www.ncbi.nlm.nih.gov/pubmed/35957766 http://dx.doi.org/10.1002/ccr3.6231 |
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