Journals / Türk Otolarengoloji Arşivi / 2003 / Cilt: 41 - Sayı: 2

Rosai-Dorfman disease (Sinus histiocytosis with massive lymphadenopathy): A case report

Rosai-Dorfman hastalığı (Masif lenfadenopatili sinüs histiositozis): Olgu sunumu

Pages
110–115
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

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

Death is a very rare complication and reported due to infiltration of vital organs. in this report the findings of a 52 years old woman who was admitted to our clinic with painless cervical lymphadenopathy is presen-ted, the findings and the treatment is compared with the literatüre.

📌 3 Key Takeaways

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Objective & Hypothesis:Rosai-Dorfman disease is a rare benign idiopatic histiocytic proliferative disorder. it is also known as sinüs histiocytosis with massive lymphadenopathy.
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Key Findings & Data:The disease is characterized by painless cervical lymphadenopathy, variably associated with fever, elevated erythrocyte sedimentation rate, weight loss, polyclonal hypergammaglobulinaemia, involvement of extra nodal organs such as brain, breast, skin, orbit ear, and gastro-intestinal tract, upper respiratory tract, spine.
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Conclusion & Impact:Death is a very rare complication and reported due to infiltration of vital organs. in this report the findings of a 52 years old woman who was admitted to our clinic with painless cervical lymphadenopathy is presen-ted, the findings and the treatment is compared with the literatüre.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Rosai-Dorfman disease is a rare benign idiopatic histiocytic proliferative disorder. it is also known as sinüs histiocytosis with massive lymphadenopathy. The disease is characterized by painless cervical lymphadenopathy, variably associated with fever, elevated erythrocyte sedimentation rate, weight loss, polyclonal hypergammaglobulinaemia, involvement of extra nodal organs such as brain, breast, skin, orbit ear, and gastro-intestinal tract, upper respiratory tract, spine. The cause of this disease is stili unknown. The precise diagnosis is performed by lymph node biopsy. Various treatment modalities include sur-gery, chemotherapy, antibiotics, steroids, radiotherapy ör the combination of these have been tried, but convenient therapy model hasn't been emerged. Most of them have been reported to regress spontaneously. Death is a very rare complication and reported due to infiltration of vital organs. in this report the findings of a 52 years old woman who was admitted to our clinic with painless cervical lymphadenopathy is presen-ted, the findings and the treatment is compared with the literatüre.

Özet

Rosai-Dorfman hastalığı idyopatik histiosit proliferasyonu ile seyreden nadir görülen bir hastalıktır. Masif lenfadenopatili sinüs histiositozis olarak da adlandırılmaktadır. Daha çok çocuklarda ve genç erişkinlerde görülür. Hastalık yaygın ağrısız lenfadenopati, yüksek ateş, lökositoz, eritrosit sedimentasyon hızında artma, poliklonal hipergamaglobulinemi, kilo kaybı ile seyrederek değişik organların tutulumuna neden olabilir. Kesin tanısı lenf bezi biyopsilerinin histopatolojik olarak incelenmesi so-nucu koyulabilmektedir. Tedavisi için antibiyotikler, kortikosteroidler, radyoterapi ve kemoterapi denenmiş ancak etkili bir tedavi şekli henüz ortaya konamamıştır. Bu hastalığa bağlı ölüm, hayati organ tutulumlarının olduğu durumlarda, çok nadir görülen bir komplikasyondur. Bu yazıda kliniğimize boynunda ağrısız, ele gelen şişlik şikayeti ile başvuran ve yapılan tetkikler ile boyun lenf bezi biyopsisi sonucu benign sinüs histiositozis tanısı konmuş olan 52 yaşında kadın hastamızın bulguları ve tedavisi literatür bilgileri ile karşılaştırılmıştır.

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Cite This Article

ÇAKLI, H., CİNGİ, E., BİLDİRİCİ, K., KÜÇÜK, S., ÖZÜDOĞRU, E. (2022). Rosai-Dorfman disease (Sinus histiocytosis with massive lymphadenopathy): A case report. Türk Otolarengoloji Arşivi, Cilt: 41 - Sayı: 2, 110–115. https://ajindex.com/articles/640064

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