Diabetic Ketoacidosis Associated with Mumps Virus Infection

Occurrence in a Patient with Macroamylasemia

  1. MARSHALL B. BLOCK, M.D.;
  2. J. EDWARD BERK, M.D.;
  3. LOUIS S. FRIDHANDLER, Ph.D.;
  4. DONALD F. STEINER, M.D.; and
  5. ARTHUR H. RUBENSTEIN, M.D.
  1. Chicago, Illinois, and Irvine, California

    Abstract

    A causal relation between infection with mumps virus and pancreatic endocrine and exocrine dysfunction is suggested by the occurrence of severe diabetic ketoacidosis and serum pancreatic amylase elevation in a patient with a significantly elevated mumps antigen titer. Sequential studies of beta cell secretion in the presence of exogenous insulin and insulin antibodies was accomplished by monitoring levels of C-peptide immunoreactivity. Secretion of proinsulin, C-peptide, and, presumably, insulin resumed after the acute episode and was associated with complete recovery of carbohydrate tolerance and cessation of insulin therapy. Serum amylase levels were persistently elevated, and a macroamylase was shown in the serum. However, the amylase released from the macroamylase complex by acidification presented different patterns at various stages of the patient's illness. Pancreatic-type amylase predominated during the acute phase, whereas the distribution of pancreatic-type and salivary-type amylase was essentially normal in samples taken several months later.

    Article and Author Information

    • ▸From the Department of Medicine, Section of Endocrinology, University of Chicago School of Medicine, Chicago, Illinois, and The Department of Medicine, University of California, Irvine, California.

    • Grant support: U.S. Public Health Service grants 5 T01 AM 051-13, AM-13941, AM-04931, and RR-55 (University of Chicago); and the John A. Hartford Foundation, Inc. (University of California, Irvine).

    • ▸Requests for reprints should be addressed to A. H. Rubenstein, M.D., Department of Medicine, Box 400, University of Chicago, 950 East 59th St., Chicago, IL 60637.

      • Received September 28, 1972.
      • Accepted January 4, 1973.
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