Orbital IgG4-Related Disease : Clinical Features and Diagnosis

المؤلفون المشاركون

Kubota, Toshinobu
Moritani, Suzuko

المصدر

ISRN Rheumatology

العدد

المجلد 2012، العدد 2012 (31 ديسمبر/كانون الأول 2012)، ص ص. 1-5، 5ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2012-06-21

دولة النشر

مصر

عدد الصفحات

5

التخصصات الرئيسية

الأمراض
الطب البشري

الملخص EN

Orbital IgG4-related disease, which can occur in adults of any age, is characterized by IgG4-positive lymphoplasmacytic infiltrations in ocular adnexal tissues.

The signs and symptoms include chronic noninflammatory lid swelling and proptosis.

Patients often have a history of allergic disease and elevated serum levels of IgG4 and IgE as well as hypergammaglobulinemia.

Orbital IgG4-related disease must be differentiated from idiopathic orbital inflammation and ocular adnexal marginal zone B-cell lymphoma to ensure appropriate and effective treatment.

Systemic steroid therapy decreases the size of the lesions, but relapse often occurs when systemic steroid therapy is discontinued.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Kubota, Toshinobu& Moritani, Suzuko. 2012. Orbital IgG4-Related Disease : Clinical Features and Diagnosis. ISRN Rheumatology،Vol. 2012, no. 2012, pp.1-5.
https://search.emarefa.net/detail/BIM-470117

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Kubota, Toshinobu& Moritani, Suzuko. Orbital IgG4-Related Disease : Clinical Features and Diagnosis. ISRN Rheumatology No. 2012 (2012), pp.1-5.
https://search.emarefa.net/detail/BIM-470117

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Kubota, Toshinobu& Moritani, Suzuko. Orbital IgG4-Related Disease : Clinical Features and Diagnosis. ISRN Rheumatology. 2012. Vol. 2012, no. 2012, pp.1-5.
https://search.emarefa.net/detail/BIM-470117

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-470117