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Volume 2012 (2012), Article ID 412896, 5 pages
Orbital IgG4-Related Disease: Clinical Features and Diagnosis
1Department of Ophthalmology, National Hospital Organization Nagoya Medical Center, 4-1-1, Sannomaru, Naka-ku, Nagoya-shi, Aichi-ken 460-0001, Japan
2Department of Pathology, National Hospital Organization Nagoya Medical Center, 4-1-1, Sannomaru, Naka-ku, Nagoya-shi, Aichi-ken 460-0001, Japan
Received 9 May 2012; Accepted 29 May 2012
Academic Editors: A. Adebajo and Z. M. Sthoeger
Copyright © 2012 Toshinobu Kubota and Suzuko Moritani. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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.
IgG4-related diseases are systemic syndromes characterized by elevated serum levels of IgG4 and IgG4-positive lymphoplasmacytic infiltrative lesions in the body. Orbital tissues are affected by IgG4-related conditions. It was first observed that Mikulicz’s disease correlated with IgG4-related disease  and later determined that IgG4-related disease can occur in any ocular adnexal tissues [2–5]. Here, we review the clinicopathological features, differential diagnosis, and treatments of orbital IgG4-related disease on the basis of a meta-analysis of 42 patients including 3 case series studies.
2. Clinical Presentation
The median age of patients with orbital IgG4-related disease is 59 years (range: 30 to 86 years) with a 1 : 1 male-to-female ratio [3–5]. Notably, there is a 1 : 3 for bilateral lacrimal lesions similar to finding in Mikulicz’s disease . Although orbital IgG4-related disease can occur in men and women of any age, many patients have a history of allergic diseases such as asthma and allergic rhinitis.
The signs and symptoms of orbital IgG4-related disease are chronic lid swelling (Figure 1) and proptosis (Figure 2), but otherwise there are only mild signs, or no signs of inflammation or periocular pain. Ocular motility is restricted mildly if at all, despite the presence of one or more enlargements of the large extraocular muscles (Figure 1). There are generally no visual disturbances, although they may occur due to apical orbital lesions (Figure 2). Imaging studies show infiltrative lesions in ocular adnexal tissues such as the lacrimal glands (Figure 1) [2–5], extraocular muscles (Figure 1) [3, 4], infraorbital nerves (Figure 2) , optic nerve sheath , lacrimal sac , and even cavernous sinus (Figure 2) or the intracranial extension . In cases of orbital IgG4-related disease, 62% have bilateral lesions, 69% have lacrimal gland involvement, and 48% have bilateral lacrimal gland involvement [3–5].
Patients with orbital IgG4-related disease sometimes have systemic IgG4-related lesions in their submandibular glands (29%), lymph nodes (14%), pancreas (5%), or bile ducts (5%) [3–5]. IgG4-related lesions in the thyroid and pituitary may also be present [7, 8]. Chronic rhinosinusitis with orbital IgG4-related lesions has similar histology (Figure 3), although nonspecific chronic rhinosinusitis can be also associated with IgG4-positive plasma cells in the lesions .
Laboratory data of patients with orbital IgG4-related disease show elevated serum levels of IgG4 and IgE, as well as hypergammaglobulinemia [2–5]. In contrast, some patients have extremely low serum levels of IgE . High IgG4 levels are associated with elevated levels of the soluble interleukin (IL-2) receptor . Sclerosing pancreatitis and cholangitis, considered as IgG4-related diseases, have lymphocytes that signal for IL-4 and IL-10 in situ . Although an etiology for the IgG4-related group of disease has been not determined yet, one plausible hypothesis for these serological and immunological abnormalities is that they result from in vivo activation of the immune system by activated Th2 cells [3, 10].
The histology of orbital IgG4-related disease includes different degrees of lymphoplasmacytic infiltration with dominant sclerosing lesions or reactive lymphoid follicle (reactive lymphoid hyperplasia, Figure 3) [2–5]. Eosinophilic infiltrations are also observed [3, 4]. Rarely, orbital IgG4-related disease may have an infiltration by lymphoplasmacytic cells and macrophages containing eosinophilic material . IgG4-related diseases in the body are characterized histologically by obliterative phlebitis; however, it is rare in orbital IgG4-related disease . Immunohistochemical analysis shows IgG4-positive plasma cells (Figure 3), which differentiate IgG4-related disease from other inflammatory conditions arising from the ocular adnexa [3, 4].
4. Differential Diagnosis
For optimal treatment and resolution, orbital IgG4-related disease must be differentiated from the following: idiopathic orbital inflammation, idiopathic orbital myositis, marginal zone B-cell lymphoma, antineutrophil cytoplasmic antibody- (ANCA-) mediated systemic vasculitis (such as Churg-Strauss syndrome and Wegener granulomatosis), and reactive lymphoid hyperplasia without IgG4-positive plasma cells (Figure 4).
Idiopathic orbital inflammations and idiopathic orbital myositis have unknown etiology but involve inflammation. They are characterized by sudden onset of orbital inflammation, periocular pain, swelling and redness of the eyelids, proptosis, ptosis, and ocular motility restrictions . These differ from the signs and symptoms of orbital IgG4-related disease. However, some cases of idiopathic orbital inflammation have atypical signs and symptoms, that is, they have lacked acute onset and inflammatory signs. In such cases, biopsy specimens are needed to differentiate idiopathic orbital inflammation from IgG4-related disease. Idiopathic orbital inflammations show lymphoplasmacytic infiltration and fibrosis with few IgG4-positive plasma cells .
Ocular adnexal marginal zone B-cell lymphomas make up the majority of lymphomas arising from the ocular adnexa. They are characterized histologically by the presence of reactive follicles in up to 64% of cases, sclerosis in up to 20% of cases, and plasma cells in up to 35% of cases . These histological characteristics are similar to those of orbital IgG4-related disease. In addition, 9% of patients with ocular adnexal marginal zone B-cell lymphomas have infiltration of IgG4-positive plasma cells and elevated serum level of IgG4 . Evidence of light chain restrictions by in situ hybridization and immunoglobulin heavy chain gene rearrangements by southern blot analysis can differentiate between marginal zone B-cell lymphomas with IgG4-positive plasma cells and IgG4-related inflammatory disorder. Ocular adnexal lymphomas are reported to arise in IgG4-related sclerosing dacryoadenitis, indicating a possible link between the two conditions . However, the causal relationship between lymphomas and IgG4-related disease remains unclear.
ANCA-related vasculitis often infiltrates in ocular adnexal lesions. The symptoms of patients with orbital lesions include periocular pain, which can differentiate these patients from those with orbital IgG4-related disease. However, the histology may be similar to that of IgG4-related disease. Thus, ANCA-related vasculitis may not only include nonspecific inflammatory lesions , but also have abundant IgG4-positive plasma cells .
Finally, Mikulicz’s disease includes symmetrical bilateral lacrimal gland enlargements and frequently correlates with IgG4-related disease . However, symmetrical bilateral lacrimal gland enlargements do not always indicate IgG4-related lesions (Figure 4).
Treatments for patients with orbital IgG4-related diseases may include systemic steroids, radiotherapy, or rituximab [3–5]. Studies of each of these treatments involved relatively few patients, making it difficult to evaluate the treatment outcomes via meta-analysis. Orbital IgG4-related diseases resolve after systemic steroid therapy, but relapse is often observed following therapy discontinuation. In Mikulicz’s disease, relapses of lesions are observed when steroids were discontinued. Therefore, it may be best to continue prednisolone at 5 to 10 mg/day or to combine prednisolone with an immunosuppressant such as azathioprine . Rituximab treatment leads to prompt clinical and serologic improvement in patients with refractory IgG4-related diseases , although recurrence is also observed after rituximab treatment ends in some patients with orbital IgG4-related disease .
Orbital IgG4-related disease has several unique characteristics that distinguish it from other orbital inflammatory conditions. Orbital IgG4-related disease differs from other IgG4-related diseases in the body in that it arises from nonglandular lesions and is not associated histologically with obliterative phlebitis.
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