Exophthalmos in a young woman with no Graves’ disease – a case report of IgG4-related orbitopathy

Abstract Background Immunoglobulin G4-related disease (IgG4-rd) is characterized by lymphoplasmacytic infiltration and tissue fibrosis. Orbital manifestations of IgG4-rd may include unilateral or bilateral proptosis, cicatricial extraocular muscle myopathy, orbital inflammation and pain which may mi...

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Main Authors: Annamaria Erdei, Zita Steiber, Csaba Molnar, Ervin Berenyi, Endre V. Nagy
Format: Article
Language:English
Published: BMC 2018-01-01
Series:BMC Ophthalmology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12886-018-0672-y
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spelling doaj-43f547bde71849a1a5274e8ad1a2958d2020-11-24T22:01:54ZengBMCBMC Ophthalmology1471-24152018-01-011811610.1186/s12886-018-0672-yExophthalmos in a young woman with no Graves’ disease – a case report of IgG4-related orbitopathyAnnamaria Erdei0Zita Steiber1Csaba Molnar2Ervin Berenyi3Endre V. Nagy4Division of Endocrinology, Department of Medicine, Faculty of Medicine, University of DebrecenDepartment of Ophthalmology, Faculty of Medicine, University of DebrecenInstitute of Pathology, Faculty of Medicine, University of DebrecenDepartment of Radiology, Faculty of Medicine, University of DebrecenDivision of Endocrinology, Department of Medicine, Faculty of Medicine, University of DebrecenAbstract Background Immunoglobulin G4-related disease (IgG4-rd) is characterized by lymphoplasmacytic infiltration and tissue fibrosis. Orbital manifestations of IgG4-rd may include unilateral or bilateral proptosis, cicatricial extraocular muscle myopathy, orbital inflammation and pain which may mimic ophthalmic Graves’ disease. Case presentation A 25-year-old woman has been referred to the endocrinology clinic, 4 months after delivery, with suspected Graves’ orbitopathy. She has had bronchial asthma and recurrent skin rashes of unknown aetiology for the last 10 years and was treated for dacryoadenitis with steroid containing eye drops 5 years ago. During pregnancy she developed eyelid swelling. After delivery, eyelid redness and retrobulbar pain evolved. Proptosis was demonstrated by Hertel’s exophthalmometry. Orbital magnetic resonance imaging showed enlarged lateral and superior rectus muscles in both orbits. Thyroid function tests were in the normal range and no thyroid stimulating hormone (TSH) receptor autoantibodies were present. The eye muscle involvement pattern raised suspicion, and the high IgG4 level with positive histology of the lacrimal gland confirmed the diagnosis of immunoglobulin G4-related orbitopathy. Rapid improvement was observed following oral methylprednisolone. Conclusions IgG4-related orbitopathy may mimic Graves’ orbitopathy. Euthyroid patients with no TSH receptor autoantibodies should be evaluated for immunoglobulin G4-related orbitopathy. Once IgG4-related orbitopathy is proven, other manifestations of IgG4-related disease have to be searched for; lifelong follow-up is warranted.http://link.springer.com/article/10.1186/s12886-018-0672-yIgG4-related orbitopathyIgG4-related diseaseGraves’ orbitopathyGraves’ diseaseCase report
collection DOAJ
language English
format Article
sources DOAJ
author Annamaria Erdei
Zita Steiber
Csaba Molnar
Ervin Berenyi
Endre V. Nagy
spellingShingle Annamaria Erdei
Zita Steiber
Csaba Molnar
Ervin Berenyi
Endre V. Nagy
Exophthalmos in a young woman with no Graves’ disease – a case report of IgG4-related orbitopathy
BMC Ophthalmology
IgG4-related orbitopathy
IgG4-related disease
Graves’ orbitopathy
Graves’ disease
Case report
author_facet Annamaria Erdei
Zita Steiber
Csaba Molnar
Ervin Berenyi
Endre V. Nagy
author_sort Annamaria Erdei
title Exophthalmos in a young woman with no Graves’ disease – a case report of IgG4-related orbitopathy
title_short Exophthalmos in a young woman with no Graves’ disease – a case report of IgG4-related orbitopathy
title_full Exophthalmos in a young woman with no Graves’ disease – a case report of IgG4-related orbitopathy
title_fullStr Exophthalmos in a young woman with no Graves’ disease – a case report of IgG4-related orbitopathy
title_full_unstemmed Exophthalmos in a young woman with no Graves’ disease – a case report of IgG4-related orbitopathy
title_sort exophthalmos in a young woman with no graves’ disease – a case report of igg4-related orbitopathy
publisher BMC
series BMC Ophthalmology
issn 1471-2415
publishDate 2018-01-01
description Abstract Background Immunoglobulin G4-related disease (IgG4-rd) is characterized by lymphoplasmacytic infiltration and tissue fibrosis. Orbital manifestations of IgG4-rd may include unilateral or bilateral proptosis, cicatricial extraocular muscle myopathy, orbital inflammation and pain which may mimic ophthalmic Graves’ disease. Case presentation A 25-year-old woman has been referred to the endocrinology clinic, 4 months after delivery, with suspected Graves’ orbitopathy. She has had bronchial asthma and recurrent skin rashes of unknown aetiology for the last 10 years and was treated for dacryoadenitis with steroid containing eye drops 5 years ago. During pregnancy she developed eyelid swelling. After delivery, eyelid redness and retrobulbar pain evolved. Proptosis was demonstrated by Hertel’s exophthalmometry. Orbital magnetic resonance imaging showed enlarged lateral and superior rectus muscles in both orbits. Thyroid function tests were in the normal range and no thyroid stimulating hormone (TSH) receptor autoantibodies were present. The eye muscle involvement pattern raised suspicion, and the high IgG4 level with positive histology of the lacrimal gland confirmed the diagnosis of immunoglobulin G4-related orbitopathy. Rapid improvement was observed following oral methylprednisolone. Conclusions IgG4-related orbitopathy may mimic Graves’ orbitopathy. Euthyroid patients with no TSH receptor autoantibodies should be evaluated for immunoglobulin G4-related orbitopathy. Once IgG4-related orbitopathy is proven, other manifestations of IgG4-related disease have to be searched for; lifelong follow-up is warranted.
topic IgG4-related orbitopathy
IgG4-related disease
Graves’ orbitopathy
Graves’ disease
Case report
url http://link.springer.com/article/10.1186/s12886-018-0672-y
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