S4728 Hydralazine-Induced ANCA Vasculitis Associated Gastrointestinal Bleed: A Case Report

Introduction: Anti-neutrophil cytoplasmic antibodies vasculitis (AV) is known to primarily affect small blood vessels and can be caused by hydralazine use. It is associated with myeloperoxidase (MPO) and proteinase 3 (PR3) antibodies. It often presents with symptoms such as fatigue, fever, weight loss, cough or hemoptysis. Here we present a case of gastroduodenal artery (GDA) bleed secondary to necrotizing vessel disease from AV. Case Description/Methods: A 51-year-old woman with past medical history of anemia, nonischemic cardiomyopathy with implantable cardioverter-defibrillator placement, type 2 diabetes, hypertension, and hyperlipidemia presents to the emergency department (ED) with hemoptysis, dyspnea, reported chills, throat pain, and melena which all began 2 days before. She had been on Eliquis for a history of deep vein thrombosis (DVT) and recently had a 20-pound weight loss over a few months. Initial labs revealed hemoglobin levels of 5.7 g/dL (baseline ∼10 g/dL), creatinine 3.1 mg/dL (baseline ∼1.1 mg/dL), and imaging of the chest revealed diffuse ground glass opacities, concerning for infection or alveolar hemorrhage. On day 3 of admission, she developed sharp abdominal pain and became hypotensive. Computed tomography abdomen/pelvis revealed large retroperitoneal hematoma surrounding the descending duodenum concerning for arterial hemorrhage and she underwent embolization of GDA with resolution of bleeding. She was found to be positive for antinuclear antibodies, p-ANCA, MPO antibody, and PR3 antibody due to being recently started on hydralazine for blood pressure control. Renal biopsy showed marked arterial intimal hyperplasia and pauci-immune necrotizing glomerulonephritis. She received plasma exchange, chemotherapy, and steroids with initial improvement and she subsequently had a pancreaticoduodenal arterial bleed requiring second embolization. She was stabilized and discharged on steroids and outpatient therapy. Discussion: While gastrointestinal (GI) bleeding from AV is rare, it can present as a serious complication, as seen in this patient. The approach to treatment includes treating underlying disease, typically with immunosuppressive agents, and managing the GI symptoms with endoscopy, embolization, or surgery. Including AV in the differential for GI bleeding in the setting of multiple organ involvement can help lead to early diagnosis and prompt management.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001146372.88008.49
Primary Topic
Vasculitis and related conditions
Type
article
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article

S4728 Hydralazine-Induced ANCA Vasculitis Associated Gastrointestinal Bleed: A Case Report

Katherine Gonzalez, H. Rahmann, Shivani Desai, Keith M. Schneider
The American Journal of Gastroenterology
Vasculitis and related conditions
article

S4728 Hydralazine-Induced ANCA Vasculitis Associated Gastrointestinal Bleed: A Case Report

Katherine Gonzalez, H. Rahmann, Shivani Desai, Keith M. Schneider
article en

Abstract

Introduction: Anti-neutrophil cytoplasmic antibodies vasculitis (AV) is known to primarily affect small blood vessels and can be caused by hydralazine use. It is associated with myeloperoxidase (MPO) and proteinase 3 (PR3) antibodies. It often presents with symptoms such as fatigue, fever, weight loss, cough or hemoptysis. Here we present a case of gastroduodenal artery (GDA) bleed secondary to necrotizing vessel disease from AV. Case Description/Methods: A 51-year-old woman with past medical history of anemia, nonischemic cardiomyopathy with implantable cardioverter-defibrillator placement, type 2 diabetes, hypertension, and hyperlipidemia presents to the emergency department (ED) with hemoptysis, dyspnea, reported chills, throat pain, and melena which all began 2 days before. She had been on Eliquis for a history of deep vein thrombosis (DVT) and recently had a 20-pound weight loss over a few months. Initial labs revealed hemoglobin levels of 5.7 g/dL (baseline ∼10 g/dL), creatinine 3.1 mg/dL (baseline ∼1.1 mg/dL), and imaging of the chest revealed diffuse ground glass opacities, concerning for infection or alveolar hemorrhage. On day 3 of admission, she developed sharp abdominal pain and became hypotensive. Computed tomography abdomen/pelvis revealed large retroperitoneal hematoma surrounding the descending duodenum concerning for arterial hemorrhage and she underwent embolization of GDA with resolution of bleeding. She was found to be positive for antinuclear antibodies, p-ANCA, MPO antibody, and PR3 antibody due to being recently started on hydralazine for blood pressure control. Renal biopsy showed marked arterial intimal hyperplasia and pauci-immune necrotizing glomerulonephritis. She received plasma exchange, chemotherapy, and steroids with initial improvement and she subsequently had a pancreaticoduodenal arterial bleed requiring second embolization. She was stabilized and discharged on steroids and outpatient therapy. Discussion: While gastrointestinal (GI) bleeding from AV is rare, it can present as a serious complication, as seen in this patient. The approach to treatment includes treating underlying disease, typically with immunosuppressive agents, and managing the GI symptoms with endoscopy, embolization, or surgery. Including AV in the differential for GI bleeding in the setting of multiple organ involvement can help lead to early diagnosis and prompt management.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 42%
Vasculitis and related conditions
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