Immune thrombocytopenic purpura (ITP) is characterized by immune-mediated platelet destruction of platelets. The condition involves the presence of autoantibodies targeting platelet membrane antigens. ITP has been documented in the literature as a rare extra-intestinal manifestation of inflammatory bowel disease (IBD). This case report aims to describe the rare association of ITP as an extra-intestinal manifestation of ulcerative colitis (UC), accompanied by a literature review.
We report the case of a 21-year-old male presenting with acute bloody diarrhea refractory to broad-spectrum antibiotic therapy. Given the patient’s significant history of intermittent persistent diarrhea, hematochezia, hematuria, and thrombocytopenia, an evaluation for relapsing IBD was undertaken. Colonoscopic biopsy findings were consistent, with UC showing mild activity, while bone marrow aspiration revealed features indicative of chronic ITP. The patient was managed with oral corticosteroids for the IBD flare and oral mesalamine, resulting in a significant improvement in platelet count. Upon follow-up, with remission of UC, it was accompanied by a complete normalization of the patient’s platelet count. ITP has been reported as a rare extra-intestinal manifestation of IBD (UC). This report emphasizes the importance of suspecting IBD in cases of unexplained thrombocytopenia, particularly in compatible clinical settings, to enable timely diagnosis and management of both conditions, ultimately improving patient outcomes.
No Approval is required letter from the Institutional Ethical Committee of Government Medical College Srinagar, Kashmir, India vide Ref. No. IRBGMC-SGR/MED/860dated 21/11/2024
Primary Language | English |
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Subjects | Internal Diseases |
Journal Section | Case Reports |
Authors | |
Publication Date | January 29, 2025 |
Submission Date | December 4, 2024 |
Acceptance Date | January 21, 2025 |
Published in Issue | Year 2025 Volume: 7 Issue: 1 |