Celiac artery dissection in polycystic kidney disease

Koichiro Yamamoto1, Kou Hasegawa1, Kosuke Oka1

  • 1Department of General Medicine Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.

Clinical Case Reports
|October 11, 2021
PubMed

Insights

Autosomal-dominant polycystic kidney disease (ADPKD) can rarely involve celiac artery dissection. Acute abdominal pain in ADPKD patients requires differentiating aortic dissection from other causes.

Area of Science:

  • Vascular Surgery
  • Nephrology
  • Gastroenterology

Background:

  • Autosomal-dominant polycystic kidney disease (ADPKD) is a common genetic disorder.
  • Complications of ADPKD typically involve the kidneys, but can affect other organs.
  • Celiac artery dissection is a rare but serious vascular emergency.

Purpose of the Study:

  • To highlight the rare complication of celiac artery dissection in ADPKD patients.
  • To emphasize the importance of differentiating celiac artery dissection from other causes of abdominal pain in ADPKD.

Main Methods:

  • Case review of ADPKD patients presenting with acute abdominal pain.
  • Review of diagnostic imaging (e.g., CT angiography) for vascular abnormalities.
  • Differential diagnosis considerations for abdominal pain in ADPKD.

Main Results:

  • Identified a rare instance of celiac artery dissection in an ADPKD patient.
  • Acute-onset abdominal pain in ADPKD necessitates exclusion of aortic and major branch dissections.
  • Celiac artery dissection presents a diagnostic challenge in the context of ADPKD.

Conclusions:

  • Celiac artery dissection is an uncommon but critical complication to consider in ADPKD patients with acute abdominal pain.
  • Vascular imaging is crucial for accurate diagnosis and timely management.
  • Early differentiation between ADPKD-related abdominal pain and dissection is vital for patient outcomes.

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