24 November 2015
: Case report
Renal Infarction Caused by Isolated Spontaneous Renal Artery Intramural Hematoma
Challenging differential diagnosis, Diagnostic / therapeutic accidents, Unusual setting of medical care, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis), Rare coexistence of disease or pathology
Sihyung ParkEF, Ga Hee LeeEF, Kyubok JinEF, Kang Min ParkF, Yang Wook KimEF, Bong Soo ParkAEFDOI: 10.12659/AJCR.895285
Am J Case Rep 2015; 16:832-836
Abstract
BACKGROUND: Acute renal infarction is an uncommon condition resulting from an obstruction or a decrease in renal arterial blood flow. Isolated spontaneous renal artery intramural hematoma is a rare cause of renal infarction.
CASE REPORT: A 46-year-old healthy man presented to our emergency room because of sudden onset of severe right flank pain. An enhanced abdominal computed tomography scan showed a low-attenuated lesion in the lateral portion of the right kidney but no visible thromboembolisms in the main vessels. Computed tomography angiography revealed acute infarction resulting from intramural hematoma of the anterior segmental artery of the right kidney, with distal occlusion.
CONCLUSIONS: The rarity and non-specific clinical presentation of renal infarction often lead to a delayed diagnosis that may result in impaired renal function. Clinical suspicion is important in the early diagnosis, and intramural hematoma of the renal artery should be considered the cause of renal infarction even in healthy patients without predisposing factors.
Keywords: Aneurysm, Dissecting - diagnosis, Diagnosis, Differential, Hematoma - diagnosis, Infarction - etiology, Kidney - blood supply, Renal Artery, Tomography, X-Ray Computed
In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.945924
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946204
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.948113
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946723
Most Viewed Current Articles
21 Jun 2024 : Case report
93,789
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
51,260
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133
20 Nov 2023 : Case report
28,206
DOI :10.12659/AJCR.941424
Am J Case Rep 2023; 24:e941424
18 Feb 2024 : Case report
23,017
DOI :10.12659/AJCR.943030
Am J Case Rep 2024; 25:e943030