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Journals / Turkish Journal of Rheumatology(.)Archives of Rheumatology / 2012 / Cilt: 27 - Sayı: 4

Sistemik Lupus Eritematöz Hastasında Melkersson-Rosenthal Sendromu:Nadir Bir Komorbidite

Melkersson-Rosenthal Syndrome in a Patient with Systemic Lupus Erythematosus: A Rare Comorbidity

Yıldız DEĞİRMENCİ
Şenol KOBAK
Ceyda HAYRETDAĞ ÖRS
Handan ÖZIŞIK KARAMAN
Pages
258–261
DOI
—
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AI Summary & Key Takeaways

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

This rare case is presented to emphasize the complete triad of MRS concomitantly occurring with SLE in this patient

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Melkersson-Rosenthal syndrome (MRS) is a rare granulomatous disease characterized by recurrent orofacial edema, facial palsy, and a fissured tongue.
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Key Findings & Data:In this article, we report a 23-year-old female case with recurrent peripheral facial palsy, mild orofacial edema, and a fissured tongue.
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Conclusion & Impact:This rare case is presented to emphasize the complete triad of MRS concomitantly occurring with SLE in this patient
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Melkersson-Rosenthal syndrome (MRS) is a rare granulomatous disease characterized by recurrent orofacial edema, facial palsy, and a fissured tongue. In this article, we report a 23-year-old female case with recurrent peripheral facial palsy, mild orofacial edema, and a fissured tongue. She had spots in her feet with a history of oral aphthous ulcers and experienced a relapse once a year. The neuroimaging results were normal, however the laboratory examination indicated systemic lupus erythematosus (SLE). This rare case is presented to emphasize the complete triad of MRS concomitantly occurring with SLE in this patient

Özet

Melkersson-Rosenthal sendromu (MRS) yineleyen orofasiyal ödem, fasiyal palsi ve fissürlü dil ile karakterize nadir bir granülomatöz hastalıktır. Bu yazıda, yineleyen periferik fasiyal paralizi, hafif orofasiyal ödem ve fissürlü dili olan 23 yaşında bir kadın olgu sunuldu. Ayaklarında lekeler ve yılda bir kez tekrarlayan oral aftöz ülser öyküsü mevcuttu. Nörogörüntüleme bulguları normaldi; ancak laboratuvar incelemeleri sistemik lupus eritematöz (SLE) tanısını destekliyordu. Bu nadir olgu, SLE hastasında görülen komplet MRS'yi vurgulamak için sunuldu

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Cite This Article

DEĞİRMENCİ, Y., KOBAK, Ş., ÖRS, C. H., KARAMAN, H. Ö. (2012). Sistemik Lupus Eritematöz Hastasında Melkersson-Rosenthal Sendromu:Nadir Bir Komorbidite. Turkish Journal of Rheumatology(.)Archives of Rheumatology, Cilt: 27 - Sayı: 4, 258–261. https://ajindex.com/articles/375982

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