Renal infarction is a relatively infrequent condition, most commonly occurring in the presence of predisposing factors, including atherosclerosis, valvular or ischemic heart disease, atrial fibrillation, endocarditis, hypercoagulability, malignancy, vasculitis, and kidney trauma.1,2 About 30% of renal infarctions, however, occur in the absence of these classic risk factors and are usually called "idiopathic."1 In this noncategorized group, an emerging diagnosis is spontaneous renal artery dissection (SRAD), which may account for several, if not the majority of cases.

Background: The improvements in dialysis have not eliminated long-term problems, including dialysis-related amyloidosis (DRA), caused by Beta-2 microglobulin deposition. Several types of scintigraphy have been tested to detect DRA, none entered the clinical practice. Aim of the study was to assess the potential of PET-FDG scan in the diagnosis of DRA. Methods: Forty-six dialysis patients with at least one PET scan (72 scans) were selected out 162 patients treated in 2016–2018. Subjective global assessment (SGA), malnutrition inflammation score (A), Charlson Comorbidity Index (CCI), were assessed at time of scan; 218 age-matched cases with normal kidney function were selected as controls. PET scans were read in duplicate. Carpal tunnel syndrome was considered a proxy for DRA. A composite “amyloid score” score considered each dialysis year = 1 point; carpal tunnel-DRA = 5 points per site. Logistic regression, ROC curves and a prediction model were built. Results: The prevalence of positive PET was 43.5% in dialysis, 5% in controls (p < 0.0001). PET was positive in 14/15 (93.3%) scans in patients with carpal tunnel. PET sensitivity for detecting DRA was 95% (specificity 64%). Carpal tunnel was related to dialysis vintage and MIS. A positive PET scan was significantly associated with dialysis vintage, MIS and amyloid score. A prediction model to explain PET positivity combined clinical score and MIS, allowing for an AUC of 0.906 (CI: 0.813–0.962; p < 0.001). Conclusions: PET-FDG may identify DRA, and may be useful in detecting cases in which inflammation favours B2M deposition. This finding, needing large-scale confirmation, could open new perspectives in the study of DRA.

severesystemicdiseaseinwhichemboliofcholesterolcrystals,comingfromarterio-scleroticaorticplaques,causetheocclusionofsmallarterialvesselsinorganorappara-tus,particularlyifhighlyvascularized(kidneysorskin).WhileCCEisrecognizedasanimportantcauseofend-stagerenalfailure,veryfewcasesarereportedinchronicdialy-sispatients.Theclinicaldifferentialdiagnosisofdistalskinlesionsindialysisisdifficult,asitincludesdifferentaffections(calciphylaxisis,vasculitis,infectiousandiatrogeniclesionsbyoralanticoagulants).Inthiscase-series,wereporton4casesdiagnosedwithCCE,overashorttimespan(oneyear),inahospitaldialysisCenterwithabout100patientsonchronictreatment(medianCharlsonindexof9). METHODS: Therewere3males,1female,medianageof78years;medianRRTvintage