Journals / ENTcase / 2016 / Cilt: 2 - Sayı: 4

ATYPICAL LANGERHANS CELL HISTIOCYTOSIS MIMICKING PRESEPTAL CELLULITIS

PRESEPTAL SELÜLİTİ TAKLİT EDEN LANGERHANS HÜCRELİ HİSTİOSİTOZ

Journal
ENTcase
Pages
205–209
Publication Date
2022-10-12
DOI
—
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AI Summary & Key Takeaways

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

Aproximately60% of patients are presented with head and neckinvolvement and often with skull base involvement.Here, we want to present a case of LCH mimickingpreseptal cellulitis as a sinusitis complication.

📌 3 Key Takeaways

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Objective & Hypothesis:Langerhans cell Histiocytosis (LCH), is a diseasecharacterized by abnormal proliferation of langerhanscells in various tissues and organs.
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Key Findings & Data:LCH can be seen at any age but it makes peak in1-3 years of age and especially in men twice moreoften than women.
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Conclusion & Impact:Aproximately60% of patients are presented with head and neckinvolvement and often with skull base involvement.Here, we want to present a case of LCH mimickingpreseptal cellulitis as a sinusitis complication.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Langerhans cell Histiocytosis (LCH), is a diseasecharacterized by abnormal proliferation of langerhanscells in various tissues and organs. The primary lesionis consistent with various number of macrophages,lymphocytes and pathological langerhans cells which ischaracterized by a clonal poliferation of Langerhanscells. LCH can be seen at any age but it makes peak in1-3 years of age and especially in men twice moreoften than women. The etiology is unknown, althoughmany factors (infection, heredity, trauma, etc.) arethought to play a role in the etiology. Aproximately60% of patients are presented with head and neckinvolvement and often with skull base involvement.Here, we want to present a case of LCH mimickingpreseptal cellulitis as a sinusitis complication.

Özet

Langerhans hücreli histiyositozis (LHH), çeşitli doku ve organlarda langerhans hücrelerinin anormal çoğalması ile karakterize bir hastalıktır. Primer lezyon makrofaj lenfosit ve langerhans hücrelerinin kolnal ve patolojik proliferasyonu ile ilşikilidir. LHH herhangi bir yaşta görülebilmekle birlikte 1-3 yaşları arasında pik yapar ve erkeklerde kadınlara oranla 2 kat daha sık görülür. Etyolojisi tam olarak bilinmemektedir ancak enfeksiyon, genetik ve travma gibi bazı nedenler etyoljide rol almaktadır. Hastaların yaklaşık 60% ı baş ve boyun tutulumu ve genellikle kafa tabanı tutulumu ile prezente olmaktadır. Bu olguda presptal selüliti klinik ve radyolojik olarak taklit eden bir LHH olgusunu sunduk.

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Cite This Article

ELBİSTANLI, M. S., ALAKHRAS, W., YAZICI, Z. M., YEĞİN, Y., ACIPAYAM, H. (2022). ATYPICAL LANGERHANS CELL HISTIOCYTOSIS MIMICKING PRESEPTAL CELLULITIS. ENTcase, Cilt: 2 - Sayı: 4, 205–209. https://ajindex.com/articles/501354

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References (7)

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