A patient with primary hyperoxaluria who developed excessive pericardial effusion despite intensive dialysis

Ali GUREL; İrem Pembegul YİGİT; Hulya TASKAPAN; Emine SAMDANCİ; Lokman Hekim TANRİVERDİ

Makale detayları

A patient with primary hyperoxaluria who developed excessive pericardial effusion despite intensive dialysis

Yazarlar:

Ali GUREL | İrem Pembegul YİGİT | Hulya TASKAPAN | Emine SAMDANCİ | Lokman Hekim TANRİVERDİ

Yayıncı:

Inonu University

Dergi:

Medicine Science 2016 Vol.5, pp.129-131

Belge Tipi:

Makale

Yayın Tarihi:

12/2015

Belge Dili:

Türkçe

Document ID (Org No.):

2000827941

Sıklık:

Üç Aylık

eISSN:

2147-0634

pISSN:

2147-0634

Özet:

 

Primary hyperoxaluria type 1 (PH type 1) is a hereditary disorder with excessive production of oxalate caused by deficient liver specific enzyme alanineglyoxylate aminotransferase (AGT). Increased oxalate production leads to calcium oxalate deposition in different organs and tissues, such as kidney, heart, nervous system, skin, bone and bone marrow. Early diagnosis is essential to prevent complications. Family history, urine oxalate assesment, oxalaemia, determination of oxalate deposits in tissues and genetic analysis are beneficial for diagnosis. Treatment should be started at early stages of the disease in order to decrease urinary saturation of calcium oxalate. High fluid intake, urinary crystallisation inhibitors and pyridoxine may be used. In chronic kidney failure patients renal replacement therapies are necessary, early transplantation is mandatory. We present a 30 year old man with PH type 1 who admitted with severe pericardial effusion, despite the fact that he was maintained both peritoneal dialysis and frequent hemodialysis.

Makale detayları

A patient with primary hyperoxaluria who developed excessive pericardial effusion despite intensive dialysis

Yazarlar: Ali GUREL | İrem Pembegul YİGİT | Hulya TASKAPAN | Emine SAMDANCİ | Lokman Hekim TANRİVERDİ

Yayıncı: Inonu University

Dergi: Medicine Science 2016 Vol.5, pp.129-131

Belge Tipi: Makale

Yayın Tarihi: 12/2015

Belge Dili: Türkçe

Document ID (Org No.): 2000827941

Sıklık: Üç Aylık

eISSN: 2147-0634

pISSN: 2147-0634

Sayı

Yazarlar:

Ali GUREL | İrem Pembegul YİGİT | Hulya TASKAPAN | Emine SAMDANCİ | Lokman Hekim TANRİVERDİ

Yayıncı:

Inonu University

Dergi:

Medicine Science 2016 Vol.5, pp.129-131

Belge Tipi:

Makale

Yayın Tarihi:

12/2015

Belge Dili:

Türkçe

Document ID (Org No.):

2000827941

Sıklık:

Üç Aylık

eISSN:

2147-0634

pISSN:

2147-0634