Kısa Rapor
BibTex RIS Kaynak Göster
Yıl 2021, Cilt: 3 Sayı: Supplement 1, 44 - 45, 07.03.2021
https://doi.org/10.46310/tjim.866999

Öz

Destekleyen Kurum

17. Uludağ İç Hastalıkları Ulusal Kış Kongresi ve 6. Bursa Aile Hekimliği Derneği Ulusal Kongresi ve 11. Uludağ İç Hastalıkları Hemşirelik Kongresi

Proje Numarası

bildiri no 78

Kaynakça

  • Torres VE, Harris PC, Pirson Y. Autosomal dominant polycystic kidney disease. Lancet. 2007 Apr 14;369(9569):1287-1301. doi: 10.1016/S0140-6736(07)60601-1.
  • Kalatharan V, Grewal G, Nash DM, Welk B, Sarma S, Pei Y, Garg AX. Stone prevalence in autosomal dominant polycystic kidney disease: A systematic review and meta-analysis. Can J Kidney Health Dis. 2020 Jul 4;7:1-19. doi: 10.1177/2054358120934628.
  • Gaur P, Gedroyc W, Hill P. ADPKD-what the radiologist should know. Br J Radiol. 2019 Jun;92(1098):20190078. doi: 10.1259/bjr.20190078.
  • Veser J, Özsoy M, Seitz C. Congenital and acquired diseases related to stone formation. Curr Opin Urol. 2018 Sep;28(5):414-9. doi: 10.1097/MOU.0000000000000522.
  • Mallett A, Patel M, Tunnicliffe DJ, Rangan GK. KHA-CARI autosomal dominant polycystic kidney disease guideline: Management of renal stone disease. Semin Nephrol. 2015 Nov;35(6):603-6.e3. doi: 10.1016/j.semnephrol.2015.10.012.
  • Ghata J, Cowley BD Jr. Polycystic kidney disease. Compr Physiol. 2017 Jun 18;7(3):945-75. doi: 10.1002/cphy.c160018.
  • Mufti UB, Nalagatla SK. Nephrolithiasis in autosomal dominant polycystic kidney disease. J Endourol. 2010 Oct;24(10):1557-61. doi: 10.1089/end.2010.0093.
  • Chapman AB, Devuyst O, Eckardt KU, Gansevoort RT, Harris T, Horie S, Kasiske BL, Odland D, Pei Y, Perrone RD, Pirson Y, Schrier RW, Torra R, Torres VE, Watnick T, Wheeler DC; Conference Participants. Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2015 Jul;88(1):17-27. doi: 10.1038/ki.2015.59.
  • Grantham JJ. Clinical practice. Autosomal dominant polycystic kidney disease. N Engl J Med. 2008 Oct 2;359(14):1477-85. doi: 10.1056/NEJMcp0804458.
  • Skolarikos A, Alivizatos G, de la Rosette J. Extracorporeal shock wave lithotripsy 25 years later: complications and their prevention. Eur Urol. 2006 Nov;50(5):981-90; discussion 990. doi: 10.1016/j.eururo.2006.01.045.

Polycystic Renal Disease Presented by Anuria and Nephrolithiasis Associated Progressive Kidney Damage: A Case Report

Yıl 2021, Cilt: 3 Sayı: Supplement 1, 44 - 45, 07.03.2021
https://doi.org/10.46310/tjim.866999

Öz

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common inherited kidney disease. Kidney stones develop in 20-30% of patients with ADPKD.Hydronephrosis, which is the most valuable radiological finding in the diagnosis of stone-related postrenal insufficiency, may be difficult to differentiate from common cysts in ADPKD patients. When kidney dysfunction develops in ADPKD patients, Glomerular Filtration Rate (GFR) loss reaches an average of 4.4 to 5.9 mL / min per year. Faster deterioration in these patients requires investigation for prerenal factors such as dehydration that triggers acute kidney damage or stone-related postrenal factors. In ADPKD, stone-related postrenal obstruction should be considered in rapid GFR losses despite negative ultrasound report for hydronephrosis as there is frequent occurrence of kidney stones and the difficulty in detecting hydronephrosis with ultrasonography (US) in these patients. Here, we present a case with ADPKD whose renal functions rapidly deteriorated while under chronic follow-up and renal function markers returned to the basal levels with the treatment of the underlying cause.

Proje Numarası

bildiri no 78

Kaynakça

  • Torres VE, Harris PC, Pirson Y. Autosomal dominant polycystic kidney disease. Lancet. 2007 Apr 14;369(9569):1287-1301. doi: 10.1016/S0140-6736(07)60601-1.
  • Kalatharan V, Grewal G, Nash DM, Welk B, Sarma S, Pei Y, Garg AX. Stone prevalence in autosomal dominant polycystic kidney disease: A systematic review and meta-analysis. Can J Kidney Health Dis. 2020 Jul 4;7:1-19. doi: 10.1177/2054358120934628.
  • Gaur P, Gedroyc W, Hill P. ADPKD-what the radiologist should know. Br J Radiol. 2019 Jun;92(1098):20190078. doi: 10.1259/bjr.20190078.
  • Veser J, Özsoy M, Seitz C. Congenital and acquired diseases related to stone formation. Curr Opin Urol. 2018 Sep;28(5):414-9. doi: 10.1097/MOU.0000000000000522.
  • Mallett A, Patel M, Tunnicliffe DJ, Rangan GK. KHA-CARI autosomal dominant polycystic kidney disease guideline: Management of renal stone disease. Semin Nephrol. 2015 Nov;35(6):603-6.e3. doi: 10.1016/j.semnephrol.2015.10.012.
  • Ghata J, Cowley BD Jr. Polycystic kidney disease. Compr Physiol. 2017 Jun 18;7(3):945-75. doi: 10.1002/cphy.c160018.
  • Mufti UB, Nalagatla SK. Nephrolithiasis in autosomal dominant polycystic kidney disease. J Endourol. 2010 Oct;24(10):1557-61. doi: 10.1089/end.2010.0093.
  • Chapman AB, Devuyst O, Eckardt KU, Gansevoort RT, Harris T, Horie S, Kasiske BL, Odland D, Pei Y, Perrone RD, Pirson Y, Schrier RW, Torra R, Torres VE, Watnick T, Wheeler DC; Conference Participants. Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2015 Jul;88(1):17-27. doi: 10.1038/ki.2015.59.
  • Grantham JJ. Clinical practice. Autosomal dominant polycystic kidney disease. N Engl J Med. 2008 Oct 2;359(14):1477-85. doi: 10.1056/NEJMcp0804458.
  • Skolarikos A, Alivizatos G, de la Rosette J. Extracorporeal shock wave lithotripsy 25 years later: complications and their prevention. Eur Urol. 2006 Nov;50(5):981-90; discussion 990. doi: 10.1016/j.eururo.2006.01.045.
Toplam 10 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular İç Hastalıkları
Bölüm Short Report
Yazarlar

Müge Karacakayalılar 0000-0002-6545-8640

Selman Candan Bu kişi benim 0000-0002-4742-296X

Mehmet Çiçek 0000-0002-0471-5404

Abdülmecit Yıldız 0000-0001-5941-9103

Münevver İrem Kök 0000-0001-5687-3642

Proje Numarası bildiri no 78
Yayımlanma Tarihi 7 Mart 2021
Gönderilme Tarihi 30 Ocak 2021
Kabul Tarihi 6 Mart 2021
Yayımlandığı Sayı Yıl 2021 Cilt: 3 Sayı: Supplement 1

Kaynak Göster

EndNote Karacakayalılar M, Candan S, Çiçek M, Yıldız A, Kök Mİ (01 Mart 2021) Polycystic Renal Disease Presented by Anuria and Nephrolithiasis Associated Progressive Kidney Damage: A Case Report. Turkish Journal of Internal Medicine 3 Supplement 1 44–45.

e-ISSN: 2687-4245 

Turkish Journal of Internal Medicine, hosted by Turkish JournalPark ACADEMIC, is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

by-nc-nd.png
2023 -TJIM.org