全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

A Case of Granulomatosis with Polyangiitis Causing Hydroureter and Hydronephrosis

DOI: 10.1155/2014/713957

Full-Text   Cite this paper   Add to My Lib

Abstract:

Granulomatosis with Polyangiitis (GPA, formerly known as Wegener) is a systemic vasculitis characterized by granulomatous involving upper and lower respiratory tract and can also cause necrotizing glomerulonephritis (Umemoto et al. 2012 and Takala et al. 2011). GPA is associated with antineutrophil cytoplasmic autoantibodies (ANCA) against serine proteinase 3 (PR3) (Takala et al. 2011, Dufour et al. 2012, and Berthoux et al. 2011). This disease usually starts with involvement of the upper and lower respiratory tracts and also can involve kidney, eyes, skin, central and peripheral nervous systems, and gastrointestinal tract (Umemoto et al. 2012, Takala et al. 2011, and Berthoux et al. 2011). We describe a case of GPA that presented with abdominal pain. Computed tomography (CT) scan with contrast showed right sided moderate hydronephrosis and hydroureter, to the level of the right common iliac artery. There was also mural segmental thickening in common iliac artery which was thought to be the cause of the ureteral obstruction and hydronephrosis. Our case shows that mural segmental thickening in common iliac artery happened due to GPA and caused hydronephrosis. In addition, most of the cases with hydronephrosis due to GPA went through urology intervention such as stent placement but in our case hydronephrosis resolved with medical management. 1. Introduction GPA is a systemic vasculitis characterized by changes involving upper and lower respiratory tracts and can also cause necrotizing glomerulonephritis [1, 2]. GPA is associated with an antineutrophil cytoplasmic autoantibodies (ANCA) against serine proteinase 3 (PR3) [2–4]. This disease usually starts with the involvement of the upper and lower respiratory tracts and also can involve kidney, eyes, skin, central and peripheral nervous systems, and gastrointestinal tract [1, 2, 4]. Usually the small vessels are the primary target of GPA; however, several recent reports have shown that the large vessels such as aorta and its branches can be involved. GPA can affect any organ, however, urologic involvement has rarely been reported. Here, we report a case of GPA presented with right kidney hydronephrosis. CT studies showed mural segmental thickening in common iliac artery, which was the cause of the ureteral obstruction and hydronephrosis. 2. Case Report A 44-year-old man was admitted to our hospital with a one-day history of sever right lower quadrant abdominal pain. He described the pain as persistent and very severe, 10/10, radiating to the flank associated with nausea and fivetime vomiting. He denied any

References

[1]  A. Umemoto, H. Ikeuchi, K. Hiromura et al., “Hydronephrosis caused by a relapse of granulomatosis with polyangiitis (Wegener's),” Modern Rheumatology, vol. 22, pp. 616–620, 2012.
[2]  J. H. Takala, H. Kautiainen, P. Finne, and M. Leirisalo-Repo, “Wegener's granulomatosis in Finland in 1981–2000: risk of dialysis-dependent renal disease,” Scandinavian Journal of Rheumatology, vol. 40, no. 4, pp. 283–288, 2011.
[3]  J.-F. Dufour, T. Le Gallou, J.-F. Cordier et al., “Urogenital manifestations in wegener granulomatosis: a study of 11 cases and review of the literature,” Medicine, vol. 91, no. 2, pp. 67–74, 2012.
[4]  E. Berthoux, M. Padilla, L. Chavez, B. Colombe, A. Bosseray, and C. Massot, “Unusual evolution in Wegener's granulomatosis: recovery of pulmonary involvement while renal disease progressed to end-stage,” Renal Failure, vol. 33, no. 10, pp. 1032–1036, 2011.
[5]  M. Roussou, S. K. Dimopoulos, M. A. Dimopoulos, and M. I. Anastasiou-Nana, “Wegener's granulomatosis presenting as a renal mass,” Urology, vol. 71, no. 3, pp. 547.e1–547.e2, 2008.
[6]  T. J. Tait and W. N. Dodds, “Wegener's granulomatosis and CREST syndrome—le Thi Huong D, Gatfosse M et al.,” Rheumatology, vol. 34, no. 5, pp. 483–484, 1995.
[7]  J. Lillaz, S. Bernardini, M. P. Algros, H. Bittard, and F. Kleinclauss, “Wegener's granulomatosis: a rare cause of hydronephrosis,” Case Reports in Medicine, vol. 2011, Article ID 814794, 3 pages, 2011.
[8]  A. Davenport, S. E. Downey, S. Goel, and A. G. MacIvert, “Wegener's granulomatosis involving the urogenital tract,” British Journal of Urology, vol. 78, no. 3, pp. 354–357, 1996.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133