S4738 Vitamin K Deficiency Secondary to Celiac Disease: A Rare Cause of Spontaneous Bleeding and Coagulopathy

Introduction: Severe vitamin K deficiency can lead to spontaneous bleeding due to its important role in coagulation and Celiac disease characterized by hypersensitivity to gluten, can exacerbate vitamin K deficiency. This case report presents a 61-year-old man who presented with bleeding due to vitamin K deficiency secondary to undiagnosed celiac disease, highlighting the diagnostic challenges and the importance of early recognition and intervention in such cases. The patient also had elevated creatine kinase (CK), which contributed to the complexity of his presentation. Case Description/Methods: A 61-year-old man presented with upper extremity swelling, bruising, and a hemoglobin level of 6.9 g/dL, a significant drop from his baseline of 14.9 g/dL. He had elevated CK and His international normalized ratio (INR) was elevated at >16 indicating severe coagulation dysfunction. The patient denied nausea, vomiting, abdominal pain, weight loss, or blood in his stool. But reported recent melena and epistaxis. He was not on blood thinners but regularly took nonsteroidal anti-inflammatory drugs (Naproxen) for chronic body aches and drank 6 beers nightly. Computed tomography scan of the abdomen revealed mild small bowel wall thickening, suggesting enteritis or ileus. Whereas, prior colonoscopy had removed multiple tubular adenomas. An upper endoscopy revealed normal esophageal mucosa, gastric erythema and scattered erosions in the antrum. The duodenum showed scalloped folds with a “cracked earth” appearance, raising suspicion for celiac disease. Pathology results confirmed severe villous blunting and increased intraepithelial lymphocytes in the duodenum, consistent with celiac disease. Gastric biopsy revealed chronic gastritis without evidence of Helicobacter pylori infection. Discussion: This case highlights a rare presentation of celiac disease. The patient's elevated INR was attributed to malabsorption of fat-soluble vitamins, particularly vitamin K, essential for clotting factor synthesis. Elevated CK levels may have been related to the underlying inflammatory process associated with celiac disease. Endoscopic findings of duodenal scalloping and biopsy results confirmed celiac disease.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001146412.55386.d2
Primary Topic
Celiac Disease Research and Management
Type
article
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article

S4738 Vitamin K Deficiency Secondary to Celiac Disease: A Rare Cause of Spontaneous Bleeding and Coagulopathy

Barakat Aburajab Altamimi, Syed Shazaib Shah, Ahmad Sandouka
The American Journal of Gastroenterology
Celiac Disease Research and Management
article

S4738 Vitamin K Deficiency Secondary to Celiac Disease: A Rare Cause of Spontaneous Bleeding and Coagulopathy

Barakat Aburajab Altamimi, Syed Shazaib Shah, Ahmad Sandouka
article en

Abstract

Introduction: Severe vitamin K deficiency can lead to spontaneous bleeding due to its important role in coagulation and Celiac disease characterized by hypersensitivity to gluten, can exacerbate vitamin K deficiency. This case report presents a 61-year-old man who presented with bleeding due to vitamin K deficiency secondary to undiagnosed celiac disease, highlighting the diagnostic challenges and the importance of early recognition and intervention in such cases. The patient also had elevated creatine kinase (CK), which contributed to the complexity of his presentation. Case Description/Methods: A 61-year-old man presented with upper extremity swelling, bruising, and a hemoglobin level of 6.9 g/dL, a significant drop from his baseline of 14.9 g/dL. He had elevated CK and His international normalized ratio (INR) was elevated at >16 indicating severe coagulation dysfunction. The patient denied nausea, vomiting, abdominal pain, weight loss, or blood in his stool. But reported recent melena and epistaxis. He was not on blood thinners but regularly took nonsteroidal anti-inflammatory drugs (Naproxen) for chronic body aches and drank 6 beers nightly. Computed tomography scan of the abdomen revealed mild small bowel wall thickening, suggesting enteritis or ileus. Whereas, prior colonoscopy had removed multiple tubular adenomas. An upper endoscopy revealed normal esophageal mucosa, gastric erythema and scattered erosions in the antrum. The duodenum showed scalloped folds with a “cracked earth” appearance, raising suspicion for celiac disease. Pathology results confirmed severe villous blunting and increased intraepithelial lymphocytes in the duodenum, consistent with celiac disease. Gastric biopsy revealed chronic gastritis without evidence of Helicobacter pylori infection. Discussion: This case highlights a rare presentation of celiac disease. The patient's elevated INR was attributed to malabsorption of fat-soluble vitamins, particularly vitamin K, essential for clotting factor synthesis. Elevated CK levels may have been related to the underlying inflammatory process associated with celiac disease. Endoscopic findings of duodenal scalloping and biopsy results confirmed celiac disease.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 44%
Celiac Disease Research and Management
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