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PMID: 1130928 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Hereditary pancreatitis. Nonspecificity of aminoaciduria and diagnosis of occult disease.

Archives of internal medicine ·Vol. 135 ·No. 6 ·1975-06-00 ·Pages 822-5

Riccardi VM, Shih VE, Holmes LB, Nardi GL

Abstract

Hereditary pancreatitis appears in many different ways and in a variety of age groups, spanning both pediatric and adult medicine. The variable expression of hereditary pancreatitis is emphasized by the difficulty in diagnosing it in a patient obviously at risk because of a severely affected father and son. The morphine prostigmine test and hypotonic duodenogram were most helpful. Aminoaciduria previously associated with this disorder is coincidental or nonspecifically related to acute pancreatic inflammation. The increased risk for pancreatic carcinoma (about 20%) is emphasized by the concern for that complication in the proband's grandfather.

MeSH Terms
Adult Amino Acids/urine Female Genes, Dominant Humans Infant Male Middle Aged Morphine Neostigmine Pancreatic Neoplasms/genetics Pancreatitis/diagnostic imaging,genetics,urine Pedigree Phenotype Radiography Risk
Chemicals
Amino Acids Neostigmine Morphine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Riccardi V M
Shih V E
Holmes L B
Nardi G L
Article Info
Journal
Archives of internal medicine
Abbr.
Arch Intern Med
ISSN
0003-9926
Published
1975-06-00
Pages
822-5
Language
English
Region
United States
NLM ID
0372440
Subset
IM
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