Abstract
Throughout his career, Dr. J. Bruce Beckwith has set the standard as physician/pathologist. Beginning with formal clinical training in pediatrics, Dr. Beckwith honed his practice of pediatric pathology to meet the needs of patient, family, and practitioner, always using a careful and compassionate blend of diagnostic accuracy and clinical practicability. Dr. Beckwith’s scientific contributions are legion and cover the diverse fields of congenital disease, forensic medicine, and neoplasia. Our fundamental understandings of in situ neuroblastoma, Beckwith-Wiedemann syndrome, sudden infant death syndrome, and Wilms tumor are all based on Dr. Beckwith’s original observations and interpretations. But equal to his research has been his extraordinary ability to communicate with, console, and inspire people of all walks of life and all disciplines, from patients and their families to students and colleagues. With this passion, Dr. Beckwith has reached far beyond the artificial confines of the laboratory and, in so doing, has earned a rightful place in the annals of pathology, pediatrics, and, indeed, humanity.
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Beckwith JB, Perrin EV. In-situ neuroblastoma: a contribution to the natural history of neural crest tumors. Am J Pathol 1963;43:1089–1104
Conference on the biology of neuroblastoma. J Pediatr Surg 1968;3(1 pt II)
Beckwith JB. Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of the kidneys and pancreas and Leydig cell hyperplasia another syndrome? Presented at the Annual Meeting of the Western Society for Pediatric Research; Los Angeles, California; November 11, 1963
Bergman AB, Beckwith JB Ray CG, eds. Proceedings of the Second International Conference on the Causes of Sudden Death in Infants. Seattle: University of Washington Press, 1970
Beckwith JB, Palmer NF. Histopathology and prognosis of Wilms tumor. Results from the first National Wilms Tumor study. Cancer 1978;41:1937–1948
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Benjamin, D.R. J. Bruce Beckwith—Physician Scientist. Pediatr Dev Pathol 8, 282–286 (2005). https://doi.org/10.1007/s10024-005-1153-x
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DOI: https://doi.org/10.1007/s10024-005-1153-x