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Posttransplant malignancy developing in an allograft is an uncommon complication of organ transplantation. The tumor may represent malignant transformation of donor or recipient cells that were previously normal, metastatic malignancy of recipient origin or malignancy transmitted from organ donor to recipient. Establishing the origin of the malignancy is critical to treatment algorithms. It is generally believed allograft removal and immunosuppression withdrawal will lead to resolution of transmitted malignancies in cases where the renal allograft is the origin. We report a male patient who developed metastatic ovarian malignancy secondary to donor transmission.

Posttransplant malignancy developing in an allograft is an uncommon complication of organ transplantation. The tumor may represent malignant transformation of donor or recipient cells that were previously normal, metastatic malignancy of recipient origin or malignancy transmitted from organ donor to recipient. Establishing the origin of the malignancy is critical to treatment algorithms. It is generally believed allograft removal and immunosuppression withdrawal will lead to resolution of transmitted malignancies in cases where the renal allograft is the origin. We report a male patient who developed metastatic ovarian malignancy secondary to donor transmission.

Reductive decomposition of spent CaSO4 was studied using a packed-bed reactor to regenerate an alternative CaO sorbent. The reactor was operated at various process conditions including an increasing CO concentration, CO/CO2 concentration ratio (0.067−1), and temperature (1123−1273 K). In all cases, N2 was used as a balancing gas. The regeneration of CaO from CaSO4 was found to be most effective in the CO−CO2−N2 atmosphere and strongly depended on the CO/CO2 concentration ratio. At 1273 K, an apparent conversion value of 0.91 for the decomposition of CaSO4 to CaO was obtained in a 2 vol % CO and 30 vol % CO2 atmosphere. On the other hand, in a CO−N2 atmosphere, CaS was predominantly produced. The SO2 absorption capacity of CaO regenerated from CaSO4 was higher than that of limestone-calcined CaO. A larger pore diameter of the regenerated CaO was considered to be responsible for the higher SO2 absorptivity.

In this paper, we present the results of time study of CAD (Computer-Aided Diagnosis) on temporal subtraction for ground-glass shadow on chest radiographs. Our results showed that the average reading time with the CAD system was significantly longer than without employing the CAD system. However, diagnostic accuracy with temporal subtraction images was slightly improved than without temporal subtraction (with; Az=0.96, without; Az=0.95). Consequently, we could interpret that the radiologist's performance was enhanced by CAD on temporal subtraction, even with longer reading time.

Purpose: to compare the diagnostic efficacy of pancreatic pharmacoangiographic CT using angiotensin II with conventional angiographic CTMaterial and Methods: Eighteen patients with space-occupying pancreatic disease were examined in this study. Pharmacoangiographic CT was performed with a 1–3-g6-ml solution of angiotensin II injected through a catheter into the celiac artery during spiral CTResults: in 17 of the 18 (94) patients, the area of pancreatic parenchymal enhancement was the same or larger at pharmacoangiographic CT than at conventional angiographic CT. the attenuation value of the pancreatic parenchyma was significantly increased at pharmacoangiographic CT (p0.0010). Although the attenuation value of tumors was also increased on images obtained after the injection of angiotensin II, the tumor-to-pancreas contrast was significantly greater at pharmacoangiographic CT (p0.0479). the mean differences in attenuation between tumor and pancreas at angiographic CT with and without angiotensin II were respectively 182 HU and 115 HUConclusion: Pharmacoangiographic CT with angiotensin II proved superior to conventional angiographic CT in the diagnosis of pancreatic disease. We therefore recommend it as a supplementary technique at the angiographic examination of patients with suspected pancreatic tumor