[PDF][PDF] Persistent fever in a patient with polycystic kidney and liver diseases and bilateral hip prostheses

CG Kwok, IR McDougall - Journal of Nuclear Medicine, 1996 - Soc Nuclear Med
Autosomal dominant polycystic kidney disease (ADPKJD) is a systemic hereditary disorder
characterized by renal cysts and commonly hepatic cysts. Reported prevalence varies …

18F-FDG PET/CT demonstrated renal and hepatic cyst infection in a patient with autosomal dominant polycystic kidney disease

D Albano, G Bosio, F Bertagna - Nuclear Medicine Review, 2016 - journals.viamedica.pl
Infection of renal or hepatic cyst is a serious complication of autosomal dominant polycystic
kidney disease (ADPKD) and early diagnosis is crucial for the correct management. We …

FDG PET/CT repeatedly demonstrated hepatic cyst infection in a patient with autosomal dominant polycystic kidney disease

CT Hsu, HR Chang, JK Lee, JH Weng… - Clinical Nuclear …, 2013 - journals.lww.com
A 70-year-old man with a history of autosomal dominant polycystic kidney disease was
referred for 18 F-FDG PET/CT scans twice at 6-month intervals due to repeated fever with …

[CITATION][C] Liver involvement in autosomal dominant polycystic kidney disease

ME Adin - New England Journal of Medicine, 2019 - Mass Medical Soc
Liver Involvement in Polycystic Kidney Disease A 51-year-old woman with autosomal
dominant polycystic kidney disease presented with chronic abdominal pain. Magnetic …

Incidental finding of autosomal dominant polycystic kidney disease with liver involvement on Tc-99m sestamibi scintigraphy

CY Chang, KH Lin, YK Chu, CP Chang… - Clinical nuclear …, 2011 - journals.lww.com
Autosomal dominant polycystic kidney disease is a systemic hereditary disease
characterized by renal cysts and sometimes involvement of the liver. We present a 65-year …

Metastatic Renal Cell Carcinoma in a Patient With Autosomal Dominant Polycystic Kidney Disease

WM Rumrill, DH Ballard - Clinical Nuclear Medicine, 2024 - journals.lww.com
Autosomal dominant polycystic kidney disease (ADPKD) manifests as multiple cysts in the
kidneys and liver but can also present with musculoskeletal and cardiovascular …

Renal and liver scans showing polycystic disease

E Meyers - J Nucl Med, 1983 - Soc Nuclear Med
Polycystic kidney disease is characterized by virtually complete obliteration of the renal
parenchyma by cysts. This rare disease appears in approximately 1 in 400 to 500 autopsies …

End-stage autosomal dominant polycystic kidney disease

JA Brown - New England Journal of Medicine, 2002 - Mass Medical Soc
Figure 1. A 45-year-old man with autosomal dominant polycystic kidney disease presented
to the urology clinic for consideration of bilateral nephrectomy as treatment for severe …

18F-FDG PET/CT diagnosis of liver cyst infection in a patient with autosomal dominant polycystic kidney disease and fever of unknown origin

J Banzo, MA Ubieto, D Gil, E Prats, P Razola… - Revista Espańola de …, 2013 - Elsevier
The diagnosis, localization and treatment of infected cysts in the kidney or liver of patients
with autosomal dominant polycystic kidney disease (ADPKD) remain a clinical challenge …

Polycystic Liver and Kidney Disease

HL Fred, I Siddique - New England Journal of Medicine, 1995 - Mass Medical Soc
Figure 1. Polycystic Liver and Kidney Disease. An asymptomatic 63-year-old man was found
on routine physical examination to have palpable hepatic nodules and ballotable kidneys …