Bilateral Orbital IgG4-Related Disease with Systemic and Corneal Involvement Showing an Excellent Response to Steroid and Rituximab Therapy: Report of a Case with 11 Years Follow-Up

Berta AI, Agaimy A, Braun JM, Manger B, Kruse FE, Holbach L (2015)

Publication Type: Journal article

Publication year: 2015

Journal

Orbit Taylor & Francis

Book Volume: 34

Pages Range: 299-301

Journal Issue: 5

DOI: 10.3109/01676830.2015.1057290

Abstract

IgG4-related disease is a newly recognized fibro-inflammatory condition. The purpose of this report is to present a patient with 11 years of follow-up, who revealed characteristic features of IgG4-related disease with systemic, orbital and corneal involvement and showed a favorable response to steroids and rituximab treatment.

Authors with CRIS profile

Abbas Agaimy Lehrstuhl für Allgemeine Pathologie und Pathologische Anatomie Bernhard Manger Professur für Rheumatologie und Klinische Immunologie

How to cite

APA:

Berta, A.I., Agaimy, A., Braun, J.M., Manger, B., Kruse, F.E., & Holbach, L. (2015). Bilateral Orbital IgG4-Related Disease with Systemic and Corneal Involvement Showing an Excellent Response to Steroid and Rituximab Therapy: Report of a Case with 11 Years Follow-Up. Orbit, 34(5), 299-301. https://doi.org/10.3109/01676830.2015.1057290

MLA:

Berta, Agnes I., et al. "Bilateral Orbital IgG4-Related Disease with Systemic and Corneal Involvement Showing an Excellent Response to Steroid and Rituximab Therapy: Report of a Case with 11 Years Follow-Up." Orbit 34.5 (2015): 299-301.

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