In stable renal transplant recipients, the GI transit parameters were significantly faster than in normal healthy volunteers. ACB sensors are versatile technologies that can be used for clinical research, because they offer an excellent opportunity to evaluate GI transit in a noninvasive manner without the use of ionizing radiation.

Liposarcomas are the most common soft tissue sarcoma of adults, and primary mediastinal liposarcomas are rare. We present a case of a 50-year-old man with primary mediastinal liposarcoma without any invasion into the surrounding structures, such as the esophagus, trachea, or left atrium of the heart. Following surgical removal of the liposarcoma, the patient has had no recurrence after one year. Surgical removal is the treatment of choice for a mediastinal liposarcoma; however, careful long-term follow-up is necessary because the recurrence rate is very high.

Kidney transplant course is often complicated with development of Donor Specifi c Antibody (DSA) which have been associated with antibody-mediated rejection (ABMR) and poor allograft survival. However the role of Non-Donor Specifi c Antibody (NDSA) in occurrence of graft rejection and loss remains controversial. We studied patients who received a kidney transplant at Harper University Hospital from 2000-2010 and grouped them based on development of antibodies. The sera of patients were routinely screened for DSA and NDSA at 6 month to one year of transplant via ELISA or Luminex assay and only those with MFI >2500 were considered positive. The patients were evaluated for occurrence of biopsy proven acute rejection which was classifi ed as cellular or ABMR per Banff criteria. Graft function was determined by most recent blood creatinine levels as of 12-31-2012 and graft loss was defi ned as need to return to dialysis or re-transplant and was censored for death. Of the 200 patients included in the study, 63 (31.5%) had NDSA only, 10 (5%) produced DSA only, 25 (12.5%) produced both and 102 (51%) non-producers at an average of 7.9 months post-transplant (range: 1-18 months). The baseline recipient characteristics were comparable except that recipients producing NDSA only or both were more likely to have had a previous transplant and therefore had higher peak PRA than non-producers and DSA only, which is suggestive of preformed NDSA due to prior sensitization. Those who produced both were more likely to be on maintenance steroid as compared to non-producing, NDSA only, and DSA only (12% vs. 32.35%, 22.22%, and 30% respectively; p<0.05). The fraction of patients with greater strength of DSA and NDSA i.e. MFI >10K was higher in the combined group than those in NDSA only (80% vs. 51.28%; p=NS) and DSA only (66.7% vs. 0%; p<0.05). There was an increased incidence of ABMR in those who produced both as compared to non-producers, NDSA only, and DSA only (20% vs. 3.92%, 1.59%, 0% respectively; p<0.01), while there was no difference in cellular rejection rates among the groups (p=NS). While the serum creatinine at last follow-up was not different between the groups, the graft loss was higher in those that produced both than others. In conclusion, NDSA alone especially at MFI <10K are not associated with increased risk of ABMR or graft loss. It is unclear if higher levels of NDSA are detrimental, especially in presence of DSA. Pre-formed and de novo IgG donor specifi c HLA antibodies (DSA) are associated with acute and chronic antibody mediated rejection (AMR) and inferior renal allograft survival. However, some patients with AMR have no detectable circulating IgG HLA DSA and it is presumed that these antibodies are either absent or bound to the allograft. IgM HLA antibodies are traditionally thought to be harmless autoantibodies and there are few studies attributing a more pathogenic role for these antibodies in renal transplantation. We retrospectively studied 24 recipients (17 male, 7 female, mean age 43.7 years), transplant...

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