Granulomatosis with polyangiitis (GPA) is an autoimmune vasculitis which rarely affects the lower genitourinary tract. We share the case of a 53-year-old man who presented with a retroperitoneal mass and thereafter developed a left multiseptated hydrocele that conditioned a testicular infarction. The pathology report of the orchidectomy was consistent with GPA.
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http://dx.doi.org/10.1016/j.reumae.2022.08.007 | DOI Listing |
Reumatol Clin (Engl Ed)
December 2024
Departamento de Medicina Interna, Hospital Angeles Lomas, Huixquilucan, Estado de México, Mexico. Electronic address:
Reumatol Clin (Engl Ed)
June 2023
Servicio de Urología, Hospital Universitario Son Espases, Palma de Mallorca, Spain.
Granulomatosis with polyangiitis (GPA) is an autoimmune vasculitis which rarely affects the lower genitourinary tract. We share the case of a 53-year-old man who presented with a retroperitoneal mass and thereafter developed a left multiseptated hydrocele that conditioned a testicular infarction. The pathology report of the orchidectomy was consistent with GPA.
View Article and Find Full Text PDFBMC Infect Dis
September 2021
Nephrology and Urology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Background: Granulomatosis with polyangiitis (GPA), also known as Wegener's granulomatosis, is an idiopathic systemic disease typically affecting the lungs, although other organs may also be involved.
Case Presentation: A 28-year-old male was admitted to Baqiyatallah university hospital in Teheran (Iran) after a 3-week history of fever and productive cough. The patient gradually developed fatigue, arthralgia, hematuria, nausea, vomiting, dyspnea, hemoptysis, weight loss, oliguria and then anuria.
Turk Thorac J
July 2017
Department of Chest Diseases, Erciyes University School of Medicine, Kayseri, Turkey.
Objectives: Eosinophilic granulomatosis with poliangiitis (EGPA) which was previously called Churg-Strauss Syndrome, is classified into eosinophilic and vasculitic phases. To characterize the eosinophilic and vasculitic phases of the disease in terms of clinical findings, serology, and treatment.
Materials And Methods: We included 15 EGPA patients in the study.
Eur J Rheumatol
June 2016
Clinic of Internal Medicine, Ankara Numune Training and Research Hospital, Ankara, Turkey.
Kaposi's sarcoma (KS), a malignant vascular tumor, can develop in patients who receive corticosteroids or immunosuppressive therapy. We report a patient with KS and granulomatosis polyangiitis (GPA). To the best of our knowledge, this is the first report regarding the co-occurrence of these two diseases.
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