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Fırat Üniversitesi Sağlık Bilimleri Veteriner Dergisi
2017, Cilt 31, Sayı 3, Sayfa(lar) 265-267
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Bir İran Kedisinde Polikistik Böbrek Hastalığı ile İlişkili Kronik Renal Yetersizlik
Kenan Çağrı TÜMER, Mustafa İSSİ
Fırat Üniversitesi, Veteriner Fakültesi, İç Hastalıkları Anabilim Dalı, Elazığ, TÜRKİYE
Anahtar Kelimeler: Kedi, poliüri, polidipsi, polikistik böbrek hastalığı, kilo kaybı
Özet
Feline polikistik böbrek hastalığı, özellikle İran kedileri ve İran kedileriyle ilişkili diğer ırklarda görülen kalıtsal bir hastalıktır. Bu olgu sunumuyla; İran ırkı bir kedide polikistik böbrek hastalığına bağlı olarak şekillenen kronik böbrek yetersizliğinin klinik, hematolojik, biyokimyasal ve ultrasonografik bulgularının paylaşılması amaçlanmıştır. Bu olgunun materyalini 2 haftadır devam eden poliüri-polidipsi, aralıklı kusma, şiddetli kilo kaybı ve iştahsızlık şikayeti ile Fırat Üniversitesi Hayvan Hastanesi İç Hastalıkları Kliniği’ne getirilen 3 yaşında, erkek, 1.8 kg ağırlığında bir İran kedisi oluşturdu. PKD ile ilişkili kronik renal yetersizlik tanısı koyulan kediye destekleyici tedaviye başlandı fakat kedi 2 hafta sonra öldü. Hayvan sahibinin izni olmadığı için nekropsi gerçekleştirilemedi. Sonuç olarak kilo kaybı poliüri ve polidipsi şikayeti ile getirilen İran kedilerinde polikistik böbrek hastalığının ayırıcı tanı tablosu içerisinde düşünülmesinin ve ülkemizde İran kedilerinde ve diğer egzotik kedilerde hastalığın prevalansının ortaya koyulması için yapılacak çalışmaların faydalı olabileceği düşünülmektedir.
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    Feline polycystic kidney disease (PKD) is a hereditery disease that affect especially Persian and Persian related cats 1. It is thought that this disease is associated with a mutation in the PKD1 gene that encodes Polycystin-1 which are the glycoprotein of the renal tubulus and responsible for cell proliferation and cell differentation 2,3.

    PKD is characterized by the formation of cysts especially in the kidney and less frequently in the liver and pancreas 4,5. Affected cats can survive for a long time without any clinical symptom 6. Because the cysts enlarge by time, they cause pressure on the kidney parenchyma and irreversible function loss occurs in the kidneys 7. Clinical signs of this disease are nonspecific and usually it is associated with chronic renal failure 4. The most common symptoms of disease are weight loss, depression, vomiting, polyuria-polydipsia, anemia and abdominal enlargement 8.

    PKD can be diagnosed as noninvasively with high confidence by ultrasonography 7,9. The sensitivity of ultrasound examination in the diagnosis of PKD was reported as 75% and 91%, in 16 weeks and 36 weeks cats respectively 10. The cysts can be seen as anechoic and distinct border, round or oval structures in the ultrasonographic examination of kidney 11.

    In this case report, it is aimed that presenting of the clinical, hematological, biochemical and ultrasonographic finding of chronic renal injury associated with PKD is reported in a Persian cat.

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    A 3 years old, 1.8 kg weight, male Persian cat was presented to Firat University Animal Hospital with a history of 2 week duration polyuria, polydipsia, severe weight loss and vomiting.

    Mild depression, severe weight loss, moderate dehydration, low body temperature (36.5 °C), elevated heart rate (164 beat/min), normal respiratory rate (32 breath/min), halitosis, ulcerative areas on the tongue and gingivitis was detected in the clinical examination. Left kidney was enlarged and irregular structure was detected at palpation.

    The blood was taken from vena cephalica antebrachii for hematological, blood gas and serum biochemical analysis. Hematological examination of blood was performed with a fully automated blood analyzer (Prokan PE-6800 Vet, China). Blood gas analysis were performed with venous blood gas analysing system (Abl-80, Radiometer Medical ApS, Denmark). Biochemical analysis were performed in Firat University Hospital Central Laboratory with automated biochemical analysing system (Advia Centaur, Siemens, Germany).Hematological, blood gas and electrolyte analysis revealed leukocystosis, normocytic normochromic anemia, acidemia, hypernatremi and high anion gap (Table 1). Serum biochemical analysis revealed hypoproteinemia, hypoalbuminemia, hyperphosphatemia, severe uremia and severe creatinaemia (Table 2).


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    Table 1: Haematology and venous blood gas analysis result


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    Table 2: Biochemical analysis results

    Sterile urinary catheter (Buster Cat Catheters, Kruuse, Denmark) was administrated to collecting urine sample. Urine spesific gravity was determined with brix refractometer (ATAGO, Japan). Decreased urine specific gravity (spesific gravity: 1010) and proteinuria was detected in urinalysis with urinary test strip (Krulab Test Strip for Urine, Kruuse, Denmark).

    The cat underwent abdominal ultrasonographic examination with micro convex transducer (GE 8C-RS, LOGIQ Book XP Vet, General Electric). Anechoic, round and distinct border structures was detected in the both kidneys (Figure 1).


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    Figure 1: Anechoic, round and distinct border cysts in left kidney

    The final diagnosis of cat was stage 4 chronic renal failure associated with PKD. The stage of chronic renal failure was evaluated as stage 4 according to International Renal Interst Society (IRIS) classification system.

    The treatment was initiated with 250 mL 0.9% NaCl solution and vitamin complex (3 mL/day p.o, Supravit, Bayer). Additionally, dietary supplementsfor supporting renal function (1 g/5 kg twice a day, Ipakitine, Novakim, Turkey) and prescription diet that contains low phosphorus and sodium was recommended. But the cat died after two weeks. The necropsy was not performed beacuse of cat’s owner didn’t allow.

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    PKD is a progressive hereditary disease that result from a mutation on the autosomal dominant gene and effects especially Persian and Persian related cats 3,12.

    The prevalence of PKD is 41.8% in France, 41% in Italy, 45% in Australia, 36.3% Slovenia and 49.2% in United Kingdom 7,9,13-15. There is no report associated with prevalence of PKD in the cat in Turkey.

    Although the cysts usually present in born, clinical signs are usually observed between 3 and 10 years of age 4. The clinical signs of PKD usually related with chronic renal failure 7. The weight loss, polyuri and polydipsia, anemia, uremic stomatitis, and abdominal enlargement are frequently encountered clinical signs 4,8. In this case, the presence of vomiting, severe weight loss, anemia, polyuria, polydipsia and age of cat were compatible with literatures.

    PKD can be diagnosed noninvasively with ultasronograpy 7,9. The presence of anechoic cystic structures have been identified within kidneys via ultrasonographic examination in different study 1,6,9. Our ultrasonographic findings are compatible with literatures.

    It has been reported that hypertension may occur and use of angiotensin converting enzymes inhibitors (ACEI) and calcium channel blockers in the management and control of hypertension in cats with chronic renal injury 16,17. Because of the systolic blood pressure was not measured in this case, any treatment was not given for hypertension.

    It is stated that hypokalemia is more common in stage 2 and stage 3 chronic renal failure but hyperkalemia is more common in stage 4 chronic renal insufficiency because decreased glomerular filtration rate and potassium retention 17,18. Na et al. 19 reported normokalemia in a woman with chronic renal failure and primary aldosteronism. They thought that normokalemia occured due to the balance between hypokalemia associated with primary aldosteronism and hyperkalemia associated with chronic renal failure. In our case we also detected normokalemia.

    Metabolic acidosis usually occurs in chronic renal insufficiency, because the kidneys can not excrete hydrogen ions and cannot reabsorb bicarbonate 17,18. Also, decreased tissue perfusion due to dehydration and elevated lactic acid concentration can contribute to exacerbation of metabolic asidosis 18. In this case, the blood gas analysis revealed severe metabolic acidosis.

    In conclusion, PKD should be considered in Persian cats that is brought with complaints of vomiting, weight loss, polyuria and polydipsia and it is thought that it may be useful to determine the prevalence of PKD in cats in Turkey.

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    1) Volta A, Manfredi S, Gnudi G, Gelati A, Bertoni G. Polycystic kidney disease in a Chartreux cat. J Feline Med Surg 2010; 12: 138-140.

    2) Lyons LA, Biller DS, Erdman CA, et al. Feline polycystic kidney disease mutation identified in PKD1. J Am Soc Nephrol 2004; 15: 2548-2555.

    3) Nivy R, Lyons LA, Aroch I, Segev G. Polycystic kidney disease in four British shorthair cats with succesful treatment of bacterial cyst infection. J Small Anim Pract 2015; 56: 585-589.

    4) Aytuğ N. Köpek ve Kedilerin İç Hastalıkları Klinik El Kitabı. 1. Baskı, Bursa: F. Özsan Matbaacılık, 2011.

    5) Wills SJ, Barrett EL, Barr FJ, et al. Evaluation of the repeatability of ultrasound scanning fort he detection of polycystic kidney disease. J Feline Med Surg.2009; 11: 993-996.

    6) Vucicevic M, Slijepcevic D, Davitkov D, et al. First report of polycystic kidney disease occurrence in Persian cats in Serbia. Vet Ital 2016; 52: 51-56.

    7) Domanjko-Petric A, Cernec D, Cotman M. Polycystic kidney disease: A review and occurence in Slovenia with comparison between ultrasound and genetic testing. J Feline Med Surg 2008; 10: 115-119.

    8) Bilal T. Kedi-Köpek İç Hastalıkları. 1. Baskı, İstanbul: Nobel, 2013.

    9) Bonazzi M, Volta A, Gnudi G, et al G. Comparison between ultrasound and genetic testing for the early diagnosis of polycystic kidney disease in Persian and exotic shorthair cats in Italy. J Feline Med Surg 2009; 11: 430-434.

    10) Biller DS, Dibartola SP, Eaton KA, et al. Inheritance of polycystic kidney disease in Persian cats. J Hered1996; 87: 1-5.

    11) Penninck D, D’anjou MA. Küçük Hayvan Ultrasonografi Atlası. Seyrek İntaş D (Çeviren). 1. Baskı. Malatya: Medipres, 2013.

    12) Eaton KA, Biller DS, Dibartola SP, Radin MJ, Wellman ML. Autosomal dominant polycystic kidney disease in Persian and Persian-cross cats. Vet Pathol 1997; 34: 117-126.

    13) Beck C, Lavelle RB. Feline polycystic kidney disease in Persian and other cats: A prospective study using ultrasonography. Aust Vet J 2001;79: 181-184.

    14) Barthez PY, Rivier P, Begon D. Prevalance of polycystic kidney disease in Persian and Persian related cats in France. J Feline Med Surg 2003; 5: 345-347.

    15) Cannon MJ, Mackay AD, Barr FJ, et al. Prevalence of polycystic kidney disease in Persian cats in the UK. Vet Rec 2001; 149: 409-411.

    16) Lefebvre HP, Toutain PL. Angiotensin-converting enzyme inhibitors in the theraphy of renal disease. J Vet Pharmacol Ther 2004; 27: 265-281.

    17) Polzin DJ. Chronic kidney disease in small animals. Vet Clin Small Anim 2011;41: 15-30.

    18) Dibartola SP. Metabolic acid-base disorders. In: Dibartola SP. (Editor). Fluid, Electrolyte and Acid-Base Disorders in Small Animal Practice. 4th Edition, Missouri: Elsevier 2012: 253-286.

    19) Na HH, Park KJ, Kim SY, Koh H. A case of primary aldosteronism with end stage renal disease. Electrolyte Blood Press 2006; 4: 83-86.

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