Klinik Araştırma
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Liver and kidney transplantation as treatments for type 1 primary hyperoxaluria

Yıl 2019, Cilt: 12 Sayı: 2, 28 - 31, 01.07.2019

Öz

Type 1 primary hyperoxaluria is an autosomal, recessive metabolic disease triggering calcium oxalate accumulation in tissues. The liver lacks the peroxisomal enzyme alanine-glyoxylate amino transferase. Clinically, patients develop kidney stones, urinary tract infections, and progressive renal failure. We evaluated liver and kidney transplantation to performed for type 1 primary hyperoxaluria in our study.
In this study, we retrospectively evaluated 7 patients with type 1 primary hyperoxaluria who underwent liver and kidney transplantation. Two main groups were established; Sequential and simultaneous liver and kidney transplantation group. Mortality rates were compared between these two groups.
Sequential liver and kidney transplantation was performed in 5 (71.4%) patients and simultaneous liver and kidney transplantation was performed in 2 (28.6%) patients. All patients died in simultaneous liver and kidney transplantation group.
Sequential liver and kidney transplantation group mortality rates were lower therefore treatment for type 1 primary hyperoxaluria more preferable.

Yıl 2019, Cilt: 12 Sayı: 2, 28 - 31, 01.07.2019

Öz

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Ayrıntılar

Birincil Dil İngilizce
Konular Cerrahi
Bölüm Araştırma Makalesi
Yazarlar

Gökhan Ertuğrul Bu kişi benim

Yayımlanma Tarihi 1 Temmuz 2019
Gönderilme Tarihi 6 Şubat 2019
Yayımlandığı Sayı Yıl 2019 Cilt: 12 Sayı: 2

Kaynak Göster

Vancouver Ertuğrul G. Liver and kidney transplantation as treatments for type 1 primary hyperoxaluria. JSurgArts. 2019;12(2):28-31.

Journal of Surgical Arts (Cerrahi Sanatlar Dergisi, ISSN:1308-0709) is indexed with, or included in, the following;  OJS, DOAJ, CROSSREF, EBSCO Host, Google Scholar, CiteFactor, MIAR Index, EuroPub Database, CABELLS, Dergipark (TUBİTAK), Türkiye Citation Index, Sobiad, Asos Index, İdeal Index, and Akademik Index.

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