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Dive into the research topics where Howard G. Worthen is active.

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The Journal of Pediatrics | 1961

The pathology of the nephrotic syndrome.

Robert L. Vernier; Howard G. Worthen; Robert A. Good

Summary The observations reviewed appear to supportthe following concepts: 1. Typical idiopathic nephrotic syndrome (nephrosis) of childhood and the other forms of the nephrotic syndrome discussed in this report are not morphologically distinguishable from one another, except for those infants showing unusual renal tubular dilatation. 2. Progressive morphologic renal abnormalities occur during the clinical expression of the nephrotic syndrome over many months and years. 3. The severity of the microscopic pathology in patients who fail to respond to treatment is related to the duration of the disease. The rate of progression of the pathology is highly variable from patient to patient, and the factors which determine the rate of progression in an individual patient are unknown. 4. Patients with idiopathic nephrotic syndrome (nephrosis) in whom renal biopsy specimens reveal minimal glomerular abnormalities usually respond to treatment with adrenocortical steroids. 5. Cessation of proteinuria followingadrenocortical steroid therapy is accompanied by improvement in the morphology of renal biopsy specimens. 6. Response to therapy with adrenocortical steroid hormones is usually associated with preservation of normal microscopic renal morphology, even though the nephrotic syndrome recurs for a number of years. 7. Patients in whom renal biopsies showmore severe glomerular pathology often fail to respond to treatment with adrenocortical steroids. Morphologic alterations in the kidney are not, however, the only factors explaining the refractory state, since some patients with minimal lesions fail to respond to treatment, while a few patients with moderately severe pathology have obtained clinical remissions after therapy. 8. Predictions of the outcome of the idiopathicnephrotic syndrome, based on the severity of the morphologic changes in a renal biopsy, are generally reliable, but exceptions occur frequently enough to make the application of this method of prediction of doubtful value in individual cases. Such predictions are not valid in patients with either the familial or infantile forms of the nephrotic syndrome. 9. Electron microscopy of renal glomerulireveals an abnormality of structure of the epithelial cell foot processes in all forms of the nephrotic syndrome which have been studied. 10. Similar abnormalities have beendemonstrated in several forms of experimental nephrotic syndrome produced in laboratory animals. 11. The severity of the epithelial cell foot process lesion appears to be related to the severity of the proteinuria. The epithelial cell foot process abnormalities are also reversible, and normal structure is found in patients responding to therapy. 12. The epithelial cell foot process lesionis the first pathologic change recognizable in the idiopathic nephrotic syndrome (nephrosis) and is present when renal glomeruli appear to be normal by light microscopy. Abnormality of structure of the endothelial cells and lamina densa are visible by electron microscopy of renal biopsy specimens obtained later in the course of the nephrotic syndrome and are correlated with the proliferative and membranous changes recognized by light microscopy. 13. Hypotheses concerning the mechanisms of proteinuria and the possible relationship of glomerular structure to the nephrotic syndrome are discussed.


The Journal of Pediatrics | 1960

II. Growth failure due to diseases of the proximal tubule

Howard G. Worthen

DYSFUNCTION of the proximal tubules is being recognized with greater frequency as a cause of growth failure. A large number of syndromes have been described in which proximal tubular function is deficient, although not all of them produce growth failure. Dwarfism is the most common sign of this type of renal disease. In some of the proximal tubular syndromes, dwarfism can be ascribed directly to the disturbance in renal function, and therapy directed to the renal defect may lead to improvement in the growth rate. In other syndromes, no evident connection can be found between the tubular defect and the growth failure, and the demonstration of renal abnormality is useful chiefly as an aid in diagnosing the underlying defect.


Pediatrics | 1961

Anaphylactoid purpura. I. Pathology of the skin and kidney and frequency of streptococcal infection.

Robert L. Vernier; Howard G. Worthen; Raymond D. A. Peterson; Eleanor Colle; Robert A. Good


JAMA Pediatrics | 1959

Infantile nephrosis; clinical, biochemical, and morphologic studies of the syndrome.

Howard G. Worthen; Robert L. Vernier; Robert A. Good


Pediatrics | 1963

SCLEREDEMA "ADULTORUMIS" IN CHILDREN Report of Three Cases with Histochemical Study and Review of World Literature

Lawrence M. Greenberg; Charles Geppert; Howard G. Worthen; Robert A. Good


JAMA Pediatrics | 1958

The de Toni-Fanconi Syndrome with Cystinosis: Clinical and Metabolic Study of Two Cases in a Family and a Critical Review on the Nature of the Syndrome

Howard G. Worthen; Robert A. Good


Pediatrics | 1977

Renal Failure During the First Year of Life

Ekkehard W. Reimold; Tran Dinh Don; Howard G. Worthen


Pediatrics | 1963

THE ASSOCIATED OCCURRENCE OF THE NEPHROTIC SYNDROME AND CONGENITAL HEART DISEASE

Keith N. Drummond; Robert L. Vernier; Howard G. Worthen; Robert A. Good


JAMA Pediatrics | 1962

Late Recurrences of the Nephrotic Syndrome Recurrence After Prolonged Remissions Induced by Adrenal Steroid Therapy

Howard G. Worthen; Alfred F. Michael; Robert L. Vernier; Robert A. Good


Pediatrics | 1974

Renal Disease in Childhood, ed. 2, by John A. James, M.B. (Edin.), M.R.C.P., D.C.H. St. Louis: The C. V. Mosby Company, 1972, 377 pp.,

Howard G. Worthen

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Robert A. Good

University of South Florida

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Ekkehard W. Reimold

University of Texas Southwestern Medical Center

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Eleanor Colle

Montreal Children's Hospital

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Keith N. Drummond

Montreal Children's Hospital

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