ENFERMEDAD POLIQUISTICA RENAL AUTOSOMICA DOMINANTE PDF

Summary Autosomal dominant polycystic kidney disease ADPKD is a common genetic pathology characterized by the development of multiple cysts in the renal parenchyma, which are the cause of the various complications that the patient presents during the course of his illness. The case of a year-old male patient with autosomal dominant polycystic kidney disease is presented, who underwent a right nephrectomy because he was a candidate for kidney transplant, who days after his surgical intervention goes to the emergency department for presenting abdominal pain diffuse of great intensity accompanied by fever of The physical examination shows a detriment of a surgical wound which is resolved by synthesis of aponeuresis. After this, during his hospitalization, the patient presented moderate intensity pain located on the left flank and accompanied by thermal rises, which is why it was decided to perform a renal ultrasound, showing a left kidney with multiple cystic images occupied by anechoic material suggestive of infection. In addition, uroculture is performed which reveals infection by Klebsiella pneumoniae producing carbapenemases, so it is decided to perform left nephrectomy. Currently, the patient survives and is in a three-week dialysis process with an acceptable quality of life.

Author:Voodoorn Kajirr
Country:Equatorial Guinea
Language:English (Spanish)
Genre:Music
Published (Last):15 June 2012
Pages:414
PDF File Size:15.90 Mb
ePub File Size:10.53 Mb
ISBN:881-9-89819-673-5
Downloads:32018
Price:Free* [*Free Regsitration Required]
Uploader:Tashura



Summary Autosomal dominant polycystic kidney disease ADPKD is a common genetic pathology characterized by the development of multiple cysts in the renal parenchyma, which are the cause of the various complications that the patient presents during the course of his illness.

The case of a year-old male patient with autosomal dominant polycystic kidney disease is presented, who underwent a right nephrectomy because he was a candidate for kidney transplant, who days after his surgical intervention goes to the emergency department for presenting abdominal pain diffuse of great intensity accompanied by fever of The physical examination shows a detriment of a surgical wound which is resolved by synthesis of aponeuresis.

After this, during his hospitalization, the patient presented moderate intensity pain located on the left flank and accompanied by thermal rises, which is why it was decided to perform a renal ultrasound, showing a left kidney with multiple cystic images occupied by anechoic material suggestive of infection. In addition, uroculture is performed which reveals infection by Klebsiella pneumoniae producing carbapenemases, so it is decided to perform left nephrectomy.

Currently, the patient survives and is in a three-week dialysis process with an acceptable quality of life. Keywords: polycystic kidney disease, nephrectomy, klebsiella pneumoniae. La terapia antimicrobiana combinada es la que mayor eficacia ha demostrado.

Nature Reviews Disease Primers. Camargo, J. Abbo, L. AAC, Cena, P. Revista Bionatura, Chapman, A. Treatment and management of autosomal dominant polycystic kidney disease. Li, Polycystic Kidney disease. Brisbane: Condon publications. Irazabala, M. Maya, J. Villegas, M. Current status of carbapenemases in Latin America. Revista de la Facultad de medicina , Montufar, F. Hernandez, C. Ran, Y. Cardiovascular ultrasound, Rojo, V.

Estudio de casos y controles. Salamancas, E. Spithoven, E. Karger, Tobal, D. Revista Medica Uruguay, Torres, V.

FOURIER SERIES AND INTEGRALS DYM PDF

Enfermedad renal poliquística (PKD)

Vushura That figure increases over time, such that essentially all patients eventually demonstrate cystic change. The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p Management of ESRD in patients with autosomal dominant polycystic kidney disease. Additionally, patients with ADPKD have a 50x increased risk of renal cell carcinomaswhich typically manifest as atypical renal cysts The mTOR pathway is regulated by polycystin-1, and its inhibition reverses renal cystogenesis in polycystic kidney enfermedad renal poliquistica. Si continua navegando, consideramos que acepta su uso.

CLANBOOK VENTRUE PDF

Poliquistosis Renal Autosómica Dominante Infectada: Presentación de un caso

.

Related Articles