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Polikistik At Nalı Böbrekli Hipertansif Bir Vaka

A Hypertensive Patient With Polycystic Horseshoe Kidney

Journal Name:

  • Türk Nefroloji, Diyaliz ve Transplantasyon Dergisi

Publication Year:

  • 2009

Key Words:

Keywords (Original Language):

Author NameUniversity of Author
Abstract (2. Language): 
Adult polycystic kidney disease is transmitted in autosomal dominant pattern with a reported incidence of 1 in 1000 to 1 in 5000 cases. Horseshoe kidney is a renal fusion anomaly with an incidence of 1 in 400 to 1 in 1800 live births. Polycystic horseshoe kidney is a rare occurrence of 1 in 134,000 to 1 in 8,000,000. We here present a patient who was admitted with left-sided flank pain, hypertension and polycystic horseshoe kidney.
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Abstract (Original Language): 
Erişkin tip polikistik böbrek hastalığı, otozomal dominant kalıtıma sahip olup, genel toplumda 1000’de 1 ile 5000’de 1 gibi bir insidans değerine sahiptir. Renal füzyon anomalisi olan at nalı böbreğin ise her 400 ila 1800 canlı doğumda 1 insidansa sahip olduğu belirtilmektedir. Polikistik at nalı böbrek anomalisi daha nadir bir durum olup, 134000 ila 8 milyonda bir görülmektedir. Yazımızda, hipertansiyon ve sol böğür ağrısı nedeniyle başvurusu sırasında polikistik at nalı böbrek anomalisi tanısı alan bir hasta konu edilmektedir.
FULL TEXT (PDF): 
PDF icon arastrmx_172977_18_pp_87-89.pdf
  • 2
87-89
  • Turkish

REFERENCES

References: 

1. Caglar K, Kibar Y, Tahmaz L, Tekin A, Yenicesu M, Vural A:
Polycystic horseshoe kidney. Clin Nephrol 2001; 55:487- 488
2. Wilson C, Azmy AF: Horseshoe kidney in children. Br J Urol 1986
Aug;58:361-363
3. Brumm FA, Becker M, Uglione A, Da Ros CT: Polycystic
horseshoe kidney. J Urol 1997; 158: 2229–2230
4. The International Polycystic Kidney Disease Consortium:
Polycystic Kidney Disease. The complete structure of the PKD1
and its protein. Cell 1995; 81: 289- 298
5. Peters DJ, Spruit L, Saris JJ, Ravine D, Sandkuijl LA, Fossdal R,
Boersma J, van Eijk R, Nørby S, Constantinou-Deltas CD, Pierides
A, Briessenden JE, Frants RR, van Ommen G.-JB, Breuning
MH: Chromosome 4 localization of a second gene for autosomal
dominant polycystic kidney disease. Nature Genet 1993; 5: 359-
362
6. Kimberling WJ, Kumar S, Gabow PA, Kenyon JB, Connolly
CJ, Somlo S: Autosomal dominant polycystic kidney disease:
localization of the second gene to chromosome 4q13-q23.
Genomics 1993; 18:467-472
7. Hoevenaren IA, Wester R, Schrier RW, McFann K, Doctor RB,
Drenth JP, Everson GT: Polycystic liver: clinical characteristics
of patients with isolated polycystic liver disease compared with
patients with polycystic liver and autosomal dominant polycystic
kidney disease. Liver Int 2008; 28:264-270
8. Peña JM, Pernaute R, Vicente de Vera C: Is ADPKD associated
with small-bowel diverticular disease? Nephrol Dial Transplant
2000; 15:1890-1891
9. Lumiaho A, Ikäheimo R, Miettinen R, Niemitukia L, Laitinen T,
Rantala A, Lampainen E, Laakso M, Hartikainen J: Mitral valve
prolapse and mitral regurgitation are common in patients with
polycystic kidney disease type 1. Am J Kidney Dis 2001; 38:1208-
1216
10. Pirson Y, Chauveau D, Torres V: Management of cerebral
aneurysms in autosomal dominant polycystic kidney disease. J Am
Soc Nephrol 2002;13:269–276
11. Kleta R, Brämswig JH. Horseshoe kidney and Turner syndrome.
Nephrol Dial Transplant 2000; 15:1094
12. Fekak H, Mezzour MH, Rabii R, Joual A, Bennani S, El Mrini M.
Management of horseshoe kidney based on a series of 36 cases.
Prog Urol 2004; 14: 485–488
13. Bozic B, Persec Z, Persec J, Borkovic Z, Galesic K. Diagnostic
and treatment of renovascular hypertension in the patient with
horseshoe kidney. Acta Med Croatica 2005; 59: 137–142
14. Ferrero Doria R, Moreno Pérez F, Calatrava Gadea S, García Víctor
F, Gassó Matoses M, Díaz Calleja E. Adult polycystic disease in
horseshoe kidney. Actas Urol Esp 2004; 28:243-244 (İspanyolca)
15. Correa RJ Jr, Paton RR: Polycystic horseshoe kidney. J Urol 1976;
116:802

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