Case report reveals effective management of mucocutaneous Behçet's disease in a child, highlighting importance of early detection.
A 12‐year‐old boy presented with recurrent oral and scrotal ulcers, papulopustular lesions, arthralgia, and a positive pathergy test. Autoimmune tests were negative; ophthalmologic and gastrointestinal assessments were reassuring. Topical therapy and colchicine produced sustained improvement. This case supports early recognition and surveillance in mucocutaneous‐predominant pediatric Behçet's disease.
No takes yet. Share an insight, caveat, or question.
Taha et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: