S6223 Treatment Failure for Recurrent Venous Thromboembolism in a Patient With Celiac Disease

Introduction: Venous thromboembolism (VTE) is a rare and conflicting extra-intestinal manifestation of celiac disease. The mechanism is likely multifactorial including deficiencies due to malabsorption, but the exact pathophysiology is unknown. Moreover, reported cases of recurrent VTE are scarce. We present a case of a young man with uncontrolled celiac disease who presented with recurrent deep vein thrombosis (DVT) despite anticoagulation. Case Description/Methods: A 27‐year‐old man with a history of alcohol use disorder, recurrent pancreatitis, and unprovoked DVT/pulmonary embolism 2 months prior presented to the emergency department for malaise, severe protein-calorie malnutrition with 30 lb weight loss, steatorrhea, and leg swelling. Patient had prior positive celiac serologies (transglutaminase IgG 14.7 and IgA >100 U/mL) but was non-compliant with diet. However, he was compliant with Eliquis from his prior admission. The patient’s vitals were stable. Physical exam was significant for bilateral lower extremity edema and rash. Labs showed profound hypoalbuminemia (1.5 g/dL), microcytic anemia (hemoglobin 6.2 g/dL), possible hemolysis (haptoglobin <20 mg/dL, lactate dehydrogenase 407 U/L), and iron studies suggestive of iron deficiency. Doppler identified acute DVTs in the right peroneal (prior location) and posterior tibial (new) veins. The hypercoagulability panel was negative, but the patient had nutritional deficiencies. The severe protein loss secondary to uncontrolled celiac disease in conjunction with pancreatic insufficiency likely contributed to deficiencies in clotting regulatory proteins, predisposing the patient to thrombotic events. The patient’s anemia was thought to be mixed autoimmune hemolytic anemia and iron deficiency secondary to celiac disease. The rash was attributed to dermatitis herpetiformis. Management included heparin for the acute DVT, strict gluten-free diet, and nutritional supplementation. Factor Xa level was within range, ruling out failure due to malabsorption, and patient was continued on Eliquis outpatient. Discussion: This case exemplifies the multifaceted complications that arise from uncontrolled celiac disease, particularly with gluten-free diet non-compliance. The relevance of this case is underscored in that although the VTE was treated on first admission, the underlying etiology was not. Given the increasing prevalence of celiac disease, clinicians must maintain a high index of suspicion for such atypical complications and emphasize dietary adherence.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001153352.95112.ce
Primary Topic
Celiac Disease Research and Management
Type
article
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article

S6223 Treatment Failure for Recurrent Venous Thromboembolism in a Patient With Celiac Disease

Kishan Patel, Jade Pace, Christopher Dorizas
The American Journal of Gastroenterology
Celiac Disease Research and Management
article

S6223 Treatment Failure for Recurrent Venous Thromboembolism in a Patient With Celiac Disease

Kishan Patel, Jade Pace, Christopher Dorizas
article en

Abstract

Introduction: Venous thromboembolism (VTE) is a rare and conflicting extra-intestinal manifestation of celiac disease. The mechanism is likely multifactorial including deficiencies due to malabsorption, but the exact pathophysiology is unknown. Moreover, reported cases of recurrent VTE are scarce. We present a case of a young man with uncontrolled celiac disease who presented with recurrent deep vein thrombosis (DVT) despite anticoagulation. Case Description/Methods: A 27‐year‐old man with a history of alcohol use disorder, recurrent pancreatitis, and unprovoked DVT/pulmonary embolism 2 months prior presented to the emergency department for malaise, severe protein-calorie malnutrition with 30 lb weight loss, steatorrhea, and leg swelling. Patient had prior positive celiac serologies (transglutaminase IgG 14.7 and IgA >100 U/mL) but was non-compliant with diet. However, he was compliant with Eliquis from his prior admission. The patient’s vitals were stable. Physical exam was significant for bilateral lower extremity edema and rash. Labs showed profound hypoalbuminemia (1.5 g/dL), microcytic anemia (hemoglobin 6.2 g/dL), possible hemolysis (haptoglobin <20 mg/dL, lactate dehydrogenase 407 U/L), and iron studies suggestive of iron deficiency. Doppler identified acute DVTs in the right peroneal (prior location) and posterior tibial (new) veins. The hypercoagulability panel was negative, but the patient had nutritional deficiencies. The severe protein loss secondary to uncontrolled celiac disease in conjunction with pancreatic insufficiency likely contributed to deficiencies in clotting regulatory proteins, predisposing the patient to thrombotic events. The patient’s anemia was thought to be mixed autoimmune hemolytic anemia and iron deficiency secondary to celiac disease. The rash was attributed to dermatitis herpetiformis. Management included heparin for the acute DVT, strict gluten-free diet, and nutritional supplementation. Factor Xa level was within range, ruling out failure due to malabsorption, and patient was continued on Eliquis outpatient. Discussion: This case exemplifies the multifaceted complications that arise from uncontrolled celiac disease, particularly with gluten-free diet non-compliance. The relevance of this case is underscored in that although the VTE was treated on first admission, the underlying etiology was not. Given the increasing prevalence of celiac disease, clinicians must maintain a high index of suspicion for such atypical complications and emphasize dietary adherence.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 43%
Celiac Disease Research and Management
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