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Gullo's Syndrome: A Case Report.

Prabhat Kumar1, Anindya Ghosh2, Vaibhav Tandon2

  • 1Senior Resident, Department of Medicine, PGIMER & Dr RML Hospital , New Delhi, India .

Journal of Clinical and Diagnostic Research : JCDR
|April 5, 2016
PubMed
Summary
This summary is machine-generated.

Benign Pancreatic Hyperenzymemia (BPH), or Gullo's Syndrome, is a rare condition of elevated pancreatic enzymes without disease. This case highlights the diagnostic challenge and the importance of exclusion in identifying BPH.

Keywords:
Benign pancreatic hyperenzymemiaCFTR mutationMacroamylasaemia

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Area of Science:

  • Gastroenterology
  • Internal Medicine
  • Biochemistry

Background:

  • Benign Pancreatic Hyperenzymemia (BPH), also known as Gullo's Syndrome, is a recently identified clinical entity.
  • It is defined by persistently elevated serum pancreatic enzymes (amylase and lipase) in the absence of any evidence of pancreatic pathology or disease.

Observation:

  • A 42-year-old female patient presented with symptoms of pneumonia.
  • Routine investigations revealed persistently elevated serum amylase and lipase levels.
  • Extensive workup for secondary causes of hyperenzymemia yielded no evidence of pancreatic disease.

Findings:

  • The patient was diagnosed with Gullo's Syndrome after a year of follow-up, during which pancreatic enzyme levels remained elevated.
  • This case represents the first reported instance of Gullo's Syndrome in the Indian subcontinent.

Implications:

  • Gullo's Syndrome is a diagnosis of exclusion, necessitating awareness of differential diagnoses for elevated pancreatic enzymes.
  • Clinicians must consider BPH in patients with unexplained hyperenzymemia, particularly when other causes are ruled out.
  • This case expands the geographical reporting of BPH and underscores its recognition in diverse clinical settings.