Journals / Türk Pediatri Arşivi / 2013 / Cilt: 48 - Sayı: 1

Kikuchi-Fujimoto disease associated with hemophagocytic syndrome

Kikuchi-Fujimoto hastalığı ile birlikte hemofagositik sendrom

Pages
71–73
Publication Date
2022-11-04
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this article, we present a case of an eight years old girl diagnosed as hemophagocytic syndrome associated with Kikuchi- Fujimoto disease. (Turk Arch Ped 2013; 48: 71-3)

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Kikuchi-Fujimoto disease is a rare condition during childhood characterized with fever and cervical lymphadenopathy.
📊
Key Findings & Data:Definitive diagnosis of the disease can only be made histologically on lymph node biopsy.
💡
Conclusion & Impact:In this article, we present a case of an eight years old girl diagnosed as hemophagocytic syndrome associated with Kikuchi- Fujimoto disease. (Turk Arch Ped 2013; 48: 71-3)
🔬Design:Research Article
📍Scope:2013 Verileri
⚙️Variables:Domain Parameters

Abstract

Kikuchi-Fujimoto disease is a rare condition during childhood characterized with fever and cervical lymphadenopathy. Definitive diagnosis of the disease can only be made histologically on lymph node biopsy. Hemophagocytic syndrome associated with Kikuchi-Fujimoto disease is especially rare. In this article, we present a case of an eight years old girl diagnosed as hemophagocytic syndrome associated with Kikuchi- Fujimoto disease. (Turk Arch Ped 2013; 48: 71-3)

Özet

Kikuchi-Fujimoto hastalığı, ateş ve boyunda lenfadenopati ile nitelenen, çocukluk çağında nadir görülen bir hastalıktır. Hastalığın kesin tanısı sadece histolojik olarak lenf nodu biyopsi ile konulabilir. Kikuchi-Fujimoto hastalığının hemofagositik sendromla birlikteliği çok daha nadirdir. Bu makalede Kikuchi- Fujimoto hastalığıyla birlikte hemofagositik sendrom tanısı alan sekiz yaşındaki kız olgu sunulmuştur. (Türk Ped Arfl 2013; 48: 71-3)

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Cite This Article

HIZARCIOĞLU, M., GÜLEZ, P., ORTAÇ, R. (2022). Kikuchi-Fujimoto disease associated with hemophagocytic syndrome. Türk Pediatri Arşivi, Cilt: 48 - Sayı: 1, 71–73. https://ajindex.com/articles/641338

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