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March 14, 2026Clinical Case Reports0 citationsOpen Access

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

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LJLilyan JarrarRFRaya FuqhaAMAhmad Wajdi Mashni

Key Points

  • 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

Abstract

ABSTRACT Clinicians should maintain a high index of suspicion for Hemophagocytic Lymphohistiocytosis in Kabuki syndrome patients who present with persistent fever, cytopenias, and organomegaly. Prompt diagnosis and multidisciplinary management are essential to improve outcomes in this rare but potentially fatal complication.

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Cite This Study

Jarrar et al. (2026) studied this question.

synapsesocial.com/papers/69b4fc1fb39f7826a300cc87https://doi.org/10.1002/ccr3.72273
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