When Rarity Hits Twice: Hemophagocytic Lymphohistiocytosis in Kabuki Syndrome—A Case Report From Palestine

Puntos clave

• The aim is to highlight the occurrence of hemophagocytic lymphohistiocytosis in a patient with Kabuki syndrome and emphasize the importance of prompt intervention.
• Case report of a patient diagnosed with Kabuki syndrome
• Observation of symptoms including fever, cytopenias, and organomegaly
• Discussion of multidisciplinary management strategies
• Patient exhibited symptoms consistent with hemophagocytic lymphohistiocytosis
• Timely diagnosis led to improved management
• Outcomes underscored the rarity and severity of the complication