S5999 Beyond the Gut: Nutcracker Syndrome as a Hidden Cause of Chronic Abdominal Pain in Surgically Altered Anatomy

Introduction: Nutcracker syndrome (NCS), defined by compression of the left renal vein between the superior mesenteric artery and the aorta, is a rare and underdiagnosed vascular disorder. While hematuria and flank pain are classic findings, gastrointestinal symptoms such as postprandial abdominal pain and nausea are underrecognized presentations that blur the line between vascular and visceral pathology. In patients with surgically altered gastrointestinal (GI) anatomy, this overlap deepens diagnostic ambiguity, and anchoring bias may delay recognition. We present a diagnostically challenging case of NCS in a patient with complex post-surgical anatomy and longstanding unexplained abdominal pain. Case Description/Methods: A 38-year-old woman with a history of partial gastrectomy (Billroth II), vagotomy, and multiple interventions for H. pylori-associated peptic ulcer disease presented with worsening postprandial abdominal pain, nausea, vomiting, and poor oral intake. Labs revealed leukocytosis (16.5), hemoglobin of 10.5 g/dL, and urinalysis with 3+ blood, 1+ protein, and >50 RBCs per high-power field. Creatinine was 0.47 mg/dL. Computed tomography imaging showed no acute bowel pathology but noted post-surgical changes and moderate constipation. Renal Doppler ultrasound and subsequent renal sonogram revealed compression of the left renal vein between the superior mesenteric artery and aorta, with an aortomesenteric distance of 0.82 cm and elevated peak velocity—findings consistent with anterior nutcracker syndrome. The patient was referred to vascular surgery for venography and further management. Discussion: This case highlights the diagnostic challenges of chronic abdominal pain in patients with altered GI anatomy, where symptoms often overlap and mislead. Nutcracker syndrome, though rare, should be considered when standard GI evaluations are inconclusive, especially with hematuria and supportive imaging. Recognizing vascular compression syndromes can prevent prolonged misdiagnosis and unnecessary procedures. A broadened differential and multidisciplinary approach are essential for complex cases of unexplained abdominal pain.

Authors

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001151456.02232.27
Primary Topic
Vascular anomalies and interventions
Type
article
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article

S5999 Beyond the Gut: Nutcracker Syndrome as a Hidden Cause of Chronic Abdominal Pain in Surgically Altered Anatomy

Christopher Bouvette, Andréa Fernandez, Ijlal Akbar Ali, Zainab Rafaqat
The American Journal of Gastroenterology
Vascular anomalies and interventions
article

S5999 Beyond the Gut: Nutcracker Syndrome as a Hidden Cause of Chronic Abdominal Pain in Surgically Altered Anatomy

Christopher Bouvette, Andréa Fernandez, Ijlal Akbar Ali, Zainab Rafaqat
article en

Abstract

Introduction: Nutcracker syndrome (NCS), defined by compression of the left renal vein between the superior mesenteric artery and the aorta, is a rare and underdiagnosed vascular disorder. While hematuria and flank pain are classic findings, gastrointestinal symptoms such as postprandial abdominal pain and nausea are underrecognized presentations that blur the line between vascular and visceral pathology. In patients with surgically altered gastrointestinal (GI) anatomy, this overlap deepens diagnostic ambiguity, and anchoring bias may delay recognition. We present a diagnostically challenging case of NCS in a patient with complex post-surgical anatomy and longstanding unexplained abdominal pain. Case Description/Methods: A 38-year-old woman with a history of partial gastrectomy (Billroth II), vagotomy, and multiple interventions for H. pylori-associated peptic ulcer disease presented with worsening postprandial abdominal pain, nausea, vomiting, and poor oral intake. Labs revealed leukocytosis (16.5), hemoglobin of 10.5 g/dL, and urinalysis with 3+ blood, 1+ protein, and >50 RBCs per high-power field. Creatinine was 0.47 mg/dL. Computed tomography imaging showed no acute bowel pathology but noted post-surgical changes and moderate constipation. Renal Doppler ultrasound and subsequent renal sonogram revealed compression of the left renal vein between the superior mesenteric artery and aorta, with an aortomesenteric distance of 0.82 cm and elevated peak velocity—findings consistent with anterior nutcracker syndrome. The patient was referred to vascular surgery for venography and further management. Discussion: This case highlights the diagnostic challenges of chronic abdominal pain in patients with altered GI anatomy, where symptoms often overlap and mislead. Nutcracker syndrome, though rare, should be considered when standard GI evaluations are inconclusive, especially with hematuria and supportive imaging. Recognizing vascular compression syndromes can prevent prolonged misdiagnosis and unnecessary procedures. A broadened differential and multidisciplinary approach are essential for complex cases of unexplained abdominal pain.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 41%
Vascular anomalies and interventions
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