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We report a case of an indwelling inferior vena cava (IVC) filter that penetrated the IVC wall after Whipple’s pancreatico-duodenectomy procedure performed in a patient with ampullary carcinoma, res...
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A 77 year old male with extramedullary plasmacytomas of the left leg. Axial T2 image with fat saturation (1.5 Tesla, TR/TE = 6400msec/87msec, slice thickness = 7mm). The masses appear hyperintense wh...
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55 years old male with remote history of spinal fixation after trauma. ...
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Fifty-nine-year-old male referred to CT scan because of an anterior mediastinal mass incidentally detected at chest x-ray for check-up. Patient refers himself asymptomatic, cholecystectomy was perform...
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Visceral artery aneurysms are infrequent lesions among other vascular diseases with an incidence of 0.01-2% in autopsy and angiographic procedures. Hepatic artery aneurysm (HAA) is a rare pathology wi...
See detailsA coronary cameral fistula (CCF) is an abnormal communication between a coronary artery and any cardiac chamber . CCF is an uncommon disorder with an incidence of 0.1% in patients undergoing coronary ...
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Case History: A two-year-old female with homocystinuria due to CBS deficiency was admitted to improve metabolic control after incidentally finding mild asymptomatic bilateral papilledema on routine o...
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Primary appendiceal adenocarcinoma is a rare malignancy, which comprises less than 0.5% of all gastrointestinal neoplasms. Most commonly, these tumors present as acute appendicitis or as a right lower...
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ABSTRACT Hydrothorax is an uncommon but well-recognized complication of pediatric peritoneal dialysis (PD). Experience with pediatric patients on PD who develop hydrothorax is limited and diagnostic ...
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Moyamoya syndrome is a rare cerebrovasculopathy of unknown etiology but is associated with multiple risk factors. Moyamoya was first discovered in Japan and is reported to have an increased prevalence...
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Figure 2. 11 year old male with primary CNS germ cell tumor. Follow-up MRI performed approximately 6 weeks later, post-chemotherapy. A. Findings: Sagittal T1-weighted MRI demonstrates interval grow...
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Xp21.2 duplication syndrome is a rare genetic disorder of undetermined prevalence and clinical relevance. As the use of chromosomal microarray has become first line for the work-up of childhood develo...
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