المؤلفون المشاركون

Sosada, Beata
Loza, Katarzyna
Bialo-Wojcicka, Ewelina

المصدر

Case Reports in Dermatological Medicine

العدد

المجلد 2014، العدد 2014 (31 ديسمبر/كانون الأول 2014)، ص ص. 1-4، 4ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2014-09-30

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الأمراض

الملخص EN

Relapsing polychondritis (RP) is a rare systemic disease characterized by recurrent, widespread chondritis of the auricular, nasal, and tracheal cartilages.

Additional clinical features include audiovestibular dysfunction, ocular inflammation, vasculitis, myocarditis, and nonerosive arthritis.

Although the cause remains unknown, the etiology is suspected to be autoimmune.

We describe a case of a 31-year-old woman with a four-month history of bilateral auricular and nasal chondritis.

Infectious and neoplastic diseases were excluded by imaging and laboratory examinations.

RP was diagnosed based on three McAdam’s criteria.

The patient was medicated with oral prednisolone and methotrexate with positive clinical response.

In this case clinical history and detailed physical examination were fundamental in concluding the correct diagnosis and administrating the appropriate medication.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Sosada, Beata& Loza, Katarzyna& Bialo-Wojcicka, Ewelina. 2014. Relapsing Polychondritis. Case Reports in Dermatological Medicine،Vol. 2014, no. 2014, pp.1-4.
https://search.emarefa.net/detail/BIM-1016981

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Sosada, Beata…[et al.]. Relapsing Polychondritis. Case Reports in Dermatological Medicine No. 2014 (2014), pp.1-4.
https://search.emarefa.net/detail/BIM-1016981

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Sosada, Beata& Loza, Katarzyna& Bialo-Wojcicka, Ewelina. Relapsing Polychondritis. Case Reports in Dermatological Medicine. 2014. Vol. 2014, no. 2014, pp.1-4.
https://search.emarefa.net/detail/BIM-1016981

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1016981