Is there any association between celiac disease, myelodysplastic symdrome and primary sclerosing cholangitis?: A rare case report

Celiac disease (CD) is an autoimmune disease characterized by a specific serological and histological profile. Hematological findings are one of the most common presentations and can sometimes be the only manifestation of the disease. In patients with unexplained isolated hematological abnormalities...

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Bibliographic Details
Published in:JGH open 2024-03, Vol.8 (3), p.e13043-n/a
Main Authors: Hamsho, Suaad, Hariri, Moudar Al, sleiay, Bilal, alhussen, Abdul hadi daher, Sleiay, Mouhammed
Format: Article
Language:English
Subjects:
Abdomen
Anemia
Antibodies
Biopsy
Blood
Bone marrow
Case Report
Case Reports
Celiac disease
Cholangitis
Consent
Endoscopy
Esophagus
Females
Hematology
Hepatitis
Hypertension
Iron
Liver cirrhosis
Medical research
myelodysplastic syndrome
Patients
primary sclerosing cholangitis
Ultrasonic imaging
ultrasound
Veins & arteries
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Summary:Celiac disease (CD) is an autoimmune disease characterized by a specific serological and histological profile. Hematological findings are one of the most common presentations and can sometimes be the only manifestation of the disease. In patients with unexplained isolated hematological abnormalities, a high index of suspicion for CD is necessary. A 33‐year‐old woman was admitted to the Department of Gastroenterology and Hepatology because of abdominal pain and fatigue. She was diagnosed with myelodysplastic syndrome. After many investigations, it is explained that she has CD. It is important to consider myelodysplastic syndrome as a hematological manifestation of CD. All patients with myelodysplasia should be investigated for CD and related conditions such as primary sclerosing cholangitis. It is important to think of myelodysplastic syndrome as a hematological manifestation of celiac disease. Celiac disease and its accompanying diseases, such as primary sclerosing cholangitis, should be investigated in all patients with myelodysplasia.
ISSN:2397-9070
2397-9070
DOI:10.1002/jgh3.13043