Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Errol Levine"'
Autor:
Errol Levine
Publikováno v:
Urologic Radiology. 13:103-106
We describe three patients with puzzling systemic illnesses in whom computed tomography (CT) led to the diagnosis of active adrenal histoplasmosis. CT was performed in two patients because of gastrointestinal symptoms and weight loss and in the third
Autor:
Olle Ekberg, Errol Levine
Publikováno v:
Abdominal Imaging. 20:179-181
Publikováno v:
Journal of Computer Assisted Tomography. 14:315-317
We describe a case in which magnetic resonance (MR) imaging of a distal femoral osteosarcoma showed transarticular skip metastases in the proximal tibia. These lesions were not found by conventional radiography, bone scintigraphy, or CT. Since detect
Autor:
Jon W. Meilstrup, Julie C. Barth, Kenneth A. Edgar, Mark A. Van Slyke, David S. Hartman, Errol Levine
Publikováno v:
The Urologic clinics of North America. 24(3)
Renal cystic disease compromises a diverse group of inherited and acquired entities. This article reviews the clinical, pathologic, and radiologic findings of eight renal cystic diseases. For each entity, the current concepts of pathogenesis and path
Autor:
J. C. Barth, M. A. Van Slyke, Errol Levine, K. A. Edgar, Jon W. Meilstrup, Henrik S. Thomsen, David S. Hartman
Publikováno v:
European radiology. 7(8)
Renal cystic disease comprises a mixed group of heritable, developmental, and acquired disorders. Because of their diverse etiology, histology, and clinical presentation, no single scheme of classification has gained acceptance. Conditions include au
Autor:
Errol Levine
Publikováno v:
Seminars in roentgenology. 30(2)
Autor:
Errol Levine
Publikováno v:
Urologic radiology. 14
Renal lymphangioma is a very rare lesion. A case of lymphangioma that presented as a small, hypercechoic renal mass on sonography in a child is reported. On CT, the lesion appeared as a low-density, enhancing renal mass. Despite its rarity, lymphangi
Autor:
Clive Levine, Errol Levine
Publikováno v:
Journal of pediatric surgery. 27(5)
A patient with an abdominal extraadrenal pheochromocytoma showed computed tomography findings of renal infarction. Selective angiography of the affected kidney showed no evidence of arterial occulusion or emboli. We postulate that the renal infarcts
Publikováno v:
Journal of pediatric surgery. 27(4)
Pheochromocytoma occurs in a familial patterm in approximately 10% of patients. Although most familial pheochromocytomas are an expression of the genetic abnormality of neuroectodermal dysplasia or the genetic syndrome of multiple endocrine neoplasia
Autor:
Errol Levine
Publikováno v:
Urologic radiology. 13(4)
Patients with end-stage kidney disease, particularly those treated with dialysis, have an increased risk of renal cell carcinoma. Renal cell carcinoma may also develop in the native kidneys of renal transplant recipients with good graft function many