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"Pancreatitis"

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Macroamylasemia as a Rare Cause of Hyperamylasemia: A Case Report
Wejdan M. Al-Johani
Korean J Fam Med 2023;44(6):347-349.   Published online November 17, 2023
DOI: https://doi.org/10.4082/kjfm.23.0195
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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  • Macroamylasemia versus Hyperamylasemia
    Vitorino Modesto dos Santos, Lister Arruda Modesto dos Santos, Taciana Arruda Modesto Sugai
    Korean Journal of Family Medicine.2024; 45(4): 233.     CrossRef
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  • 81 Download
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A Case of Acute Pancreatitis: An Unusual Manifestation of Acute Q Fever
Sondess Arfa, Rebeh Bougossa, Mouna Brahem, Ichrak Bannour, Jihene Chelli, Olfa Berriche
Korean J Fam Med 2023;44(3):177-180.   Published online May 20, 2023
DOI: https://doi.org/10.4082/kjfm.22.0041
Acute pancreatitis is a sudden inflammation affecting the exocrine region of the pancreatic parenchyma. Infectious etiologies are rare. Here we report an exceptional case of a 44-year-old woman from a rural area who was referred to our hospital with fever and abdominal pain. A physical examination revealed pale skin and epigastric tenderness. Thoracoabdominal computed tomography revealed a Balthazar score of D. Serum laboratory findings revealed hemolytic anemia, hepatic cytolysis, and high C-reactive protein level. Calcium and lipase levels were normal. There was no history of recent trauma, alcohol consumption, or drug intoxication. The diagnosis of “query” pancreatitis was confirmed by serological Coxiella burnetii positivity. Oral doxycycline 200 mg daily was initiated. The clinical evolution was favorable. To our knowledge, no association between acute pancreatitis and hemolytic anemia caused by C. burnetii was reported previously. Q fever must be considered in cases of acute pancreatitis, especially when the patient is from a rural area or has a high-risk profession.
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  • 87 Download
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