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Your search keyword '"Suzanne Merrill"' showing total 2 results
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2 results on '"Suzanne Merrill"'

1. Histologic Heterogeneity of Extirpated Renal Cell Carcinoma Specimens: Implications for Renal Mass Biopsy

Author

Lauren Nahouraii, Jordan Allen, Suzanne Merrill, Erik Lehman, Matthew Kaag, and Jay Raman

Subjects
heterogeneity, histology, renal cell carcinoma, renal mass biopsy, renal tumors, Diseases of the genitourinary system. Urology, RC870-923, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract

Pathologic characteristics of extirpated renal cell carcinoma (RCC) specimens 4 cm exhibit considerable histologic heterogeneity and may harbor elements that are not easily appreciated with limited renal sampling. Therefore, if RMB is considered for renal masses greater than 4 cm or those that abut sinus fat, a multi-quadrant biopsy approach is necessary to ensure adequate sampling and characterization of the mass.

Published
2020
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2. Early occurrence of end-stage renal disease in a patient with infantile nephropathic cystinosis

Author

Gary D. Shackelford, Barbara R. Cole, Jerry A. Schneider, John M. Kissane, Samuel So, Margaret L. Smith, Jill Cottel, Raoul D. Nelson, Suzanne Merrill, Eric Marcusson, and H. William Schnaper

Subjects
Pediatrics, medicine.medical_specialty, Cystinosis, Kidney, End stage renal disease, Nephropathy, Lesion, Tubulopathy, medicine, Humans, Infantile nephropathic cystinosis, business.industry, Infant, Fibroblasts, medicine.disease, Surgery, Clone Cells, Transplantation, Pediatrics, Perinatology and Child Health, Cystine, Kidney Failure, Chronic, Female, medicine.symptom, Complication, business
Abstract

We report the case of a patient with infantile nephropathic cystinosis who required renal transplantation at age 30 months. Exhaustive evaluation did not identify a cause of progressive renal failure other than cystinosis. The patient's genetic lesion was allelic with those of other patients with cystinosis; fusion of this patient's fibroblasts with fibroblasts from another patient with infantile nephropathic cystinosis did not demonstrate complementation of the biochemical defect.

Published
1992

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