ArticleKorean journal of family medicine2023
Macroamylasemia as a Rare Cause of Hyperamylasemia: A Case Report.
Article in Korean journal of family medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed, 3 citations in OpenAlex.
- Macroamylasemia versus Hyperamylasemia.Korean journal of family medicine · 2024Article
- A rare convergence: Gangrenous bowel secondary to closed-loop obstruction with elevated urine amylase levels - A comprehensive case report.Malaysian family physician : the official journal of the Academy of Family Physicians of Malaysia · 2024Article
- Macroamylasemia in a Two-Year-Old Boy as the First Manifestation of Celiac Disease: A Case Report.Case reports in gastroenterologyArticle
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Authors and funding
1 author at 1 institution in 1 country.
Funding
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Abstract
Macroamylasemia is a rare condition characterized by the formation of an amylase-globulin complex that is too large to be readily excreted by the kidneys and leads to elevated serum amylase levels. It is a benign condition lacking severe signs and symptoms that does not require treatment. This paper presents a case of a middle-aged man with unexplained elevated serum amylase levels. Despite an initially elevated triglyceride level, clinical findings, laboratory test results, and radiological findings were not suggestive of pancreatitis. The ratio of renal amylase clearance to creatinine clearance was calculated at <1%, consistent with macroamylasemia. No specific treatment was given, and he was monitored periodically. Nevertheless, macroamylasemia is a diagnostic challenge because of the need to differentiate it from other causes of hyperamylasemia to avoid unnecessary tests and treatments.
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Registered trials
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