Spontaneous renal artery dissection complicated by renal infarction: A case report and review of the literature
Abstract Introduction Renal artery dissection is a rare cause of abdominal pain. The renal arteries are the commonest site of primary dissection involving visceral vessels but spontaneous bilateral dissection is extremely rare. Presentation of case We present a case of spontaneous bilateral renal ar...
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Published in | International journal of surgery case reports Vol. 3; no. 7; pp. 257 - 259 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ltd
01.01.2012
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Abstract Introduction Renal artery dissection is a rare cause of abdominal pain. The renal arteries are the commonest site of primary dissection involving visceral vessels but spontaneous bilateral dissection is extremely rare. Presentation of case We present a case of spontaneous bilateral renal artery dissection in a previously fit 43-year-old man who presented with right iliac fossa pain. He was treated conservatively with anticoagulation for 6 months, with resolution of the dissections on imaging at 6-month follow-up. Discussion The presentation of spontaneous renal artery dissection is non-specific, making it a diagnostic challenge. Computed Tomography angiography is now the gold standard for diagnosis and follow-up of these patients. Conclusion This case highlights the importance of considering other causes of abdominal pain in a young man with normal initial investigations and the role of conservative management. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2210-2612 2210-2612 |
DOI: | 10.1016/j.ijscr.2012.03.009 |