KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Polycystic Liver Disease.

نویسندگان

  • Judy Savige
  • Andrew Mallett
  • David J Tunnicliffe
  • Gopala K Rangan
چکیده

a. We recommend screening for polycystic liver disease in all patients diagnosed with autosomal dominant polycystic kidney disease using abdominal ultrasound (1C). b. We recommend that all female patients with autosomal dominant polycystic kidney disease and liver cysts undergo counseling regarding the risks of pregnancy and exogenous estrogen exposure in worsening liver cyst growth (1C). c. We recommend that females at risk of symptoms from hepatic cysts avoid estrogen supplements (1D). d. We recommend that a multidisciplinary team (hepatologist, hepatobiliary surgeon, interventional radiologist, and nephrologist) care for patients with severe polycystic liver disease associated with autosomal dominant polycystic kidney disease (1D).

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of End-Stage Kidney Disease.

those that are being considered as potential kidney donors, need to be carefully screened and excluded from having ADPKD (KHA-CARI ADPKD Guidelines: Genetics, Imaging, and Screening subtopics), prior to living donor transplantation. Nephrectomy of a polycystic kidney prior to the time of transplantation may be required due to insufficient intra-abdominal space for the new allograft. Nephrectomy...

متن کامل

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Renal Stone Disease.

a. We recommend that unenhanced computed tomography is the preferred imaging modality for the diagnosis of suspected nephrolithiasis in autosomal dominant polycystic kidney disease (1B). b. We recommend that patients with autosomaldominant polycystic kidney disease complicated by nephrolithiasis should be investigated for predisposing urinary metabolic abnormalities (1C) and we suggest receive ...

متن کامل

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Screening for Polycystic Kidney Disease.

a. We recommend prior to screening at-risk individuals should receive appropriate counseling regarding the potential benefits and risks of making the diagnosis of autosomal dominant polycystic kidney disease from their general practitioner in consultation with a clinical geneticist or nephrologist (2A). b. We recommend that screening of individuals who are at-risk (50% chance) be performed by r...

متن کامل

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Psychosocial Care.

! Explore and validate patient concerns and frustrations about the unpredictability, volatility, and intensity of chronic renal pain. ! Provide strategies and counseling on how to manage the psychological, emotional, and lifestyle impact of pain; and to limit its interference with lifestyle. Behavioral therapy, peer support, emotional disclosure, and online programs have been found to be effect...

متن کامل

KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Genetic Testing for Diagnosis.

a. We recommend that the standard methodology for genetic diagnosis of autosomal dominant polycystic kidney disease is polymerase chain reaction (PCR) amplification (including long-range PCR for the first 33 exons of PKD1) followed by Sanger sequencing (1A) or next-generation sequencing where available (1D). b. We suggest that individuals with a clinical diagnosis of autosomal dominant polycyst...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Seminars in nephrology

دوره 35 6  شماره 

صفحات  -

تاریخ انتشار 2015