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Abstract Crohn’s disease (CD) is an inflammatory bowel disease affecting the digestive tract, the incidence of which is on the rise worldwide. The most common clinical manifestation of hemophilia is arthropathy secondary to recurrent joint effusions and chronic synovitis. This article reports on a rare 25-year-old male patient with both hemophilic arthropathy and Crohn’s disease who was at risk for pathogenic gastrointestinal bleeding. After undergoing endoscopic pathologic testing and genetic testing, a multidisciplinary expert work-up of a treatment and nutritional plan was performed. The patient improved clinically and adhered to conservative treatment. This case report is the first report of this rare co-morbidity, demonstrating the highly pathogenic mutation locus and summarizing the clinical experience of early diagnosis and treatment.
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Zhongyi Zhang
Lei Chen
Haojing Zhou
BMC Musculoskeletal Disorders
Zhejiang Chinese Medical University
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Zhang et al. (Fri,) studied this question.
www.synapsesocial.com/papers/68e62c1bb6db6435875be497 — DOI: https://doi.org/10.1186/s12891-024-07610-y