Literature DB >> 22341851

The immunobiology and clinical characteristics of IgG4 related diseases.

Hiroki Takahashi1, Motohisa Yamamoto, Tetsuya Tabeya, Chisako Suzuki, Yasuyoshi Naishiro, Yasuhisa Shinomura, Kohzoh Imai.   

Abstract

Having the characteristic features of elevated serum IgG4 levels and prominent infiltration of IgG4-positive plasma cells with fibrosis in lesions, Mikulicz's disease (MD) has been recognized as an IgG4-related disease (IgG4-RD). Although incidence of autoimmune pancreatitis (AIP), one of the organ characteristics of IgG4-RD, has been internationally reported, there are only a few such reports of IgG4-related MD. The limited number of reports might be attributable to the low recognition of IgG4-related MD as a clinical entity as well as its misdiagnosis as Sjögren's syndrome (SS). Thus, we compared several clinical features of MD with SS to improve proper clinical diagnosis of MD in the clinical setting. A total of 70 SS and 70 MD cases evaluated at Sapporo Medical University Hospital were retrospectively analyzed. In SS patients, sicca symptoms were the most frequent (87%), followed by articular symptoms (23%), while lacrimal and salivary gland swelling were a rare (10%) and transient manifestation. In contrast, lacrimal or salivary gland swelling was observed in all patients with MD. Although nearly 60% of MD patients complained of sicca syndrome, skin rash and arthralgia were rare symptoms. Hypergammaglobulinemia was recognized in both SS and MD patients, but the occurrence of autoantibodies in patients with IgG4-related MD was low. Extraglandular organ involvement, often involving the retroperitoneum, pancreas, kidney and lung, was often discovered at the time of IgG4-related MD diagnosis. Although corticosteroid therapy tended to delay the hypofunction of salivary gland in SS patients, recovery of decreased function of salivary glands were observed in IgG4-related MD patients. These results suggest the beneficial effect of aggressive corticosteroid intervention in patients with IgG4-related MD. Although SS and MD are both chronic inflammatory diseases affecting the lacrimal and salivary glands, their clinical features and corticosteroid responsiveness are different. Thus, differential diagnosis of these conditions is warranted.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22341851     DOI: 10.1016/j.jaut.2012.01.007

Source DB:  PubMed          Journal:  J Autoimmun        ISSN: 0896-8411            Impact factor:   7.094


  13 in total

Review 1.  Mechanisms and assessment of IgG4-related disease: lessons for the rheumatologist.

Authors:  Motohisa Yamamoto; Hiroki Takahashi; Yasuhisa Shinomura
Journal:  Nat Rev Rheumatol       Date:  2013-12-03       Impact factor: 20.543

2.  Mikulicz's Disease With Immune Thrombocytopenia: A New Immunoglobulin G4-Mediated Disorder and Literature Review.

Authors:  Shu Li; Cong Deng; Jinwei Chen; Fen Li
Journal:  Arch Rheumatol       Date:  2018-11-30       Impact factor: 1.472

3.  IgG4-related lung disease with atypical CT imaging: a case report.

Authors:  Jiaxuan Zhou; Xian Li; Qingsi Zeng
Journal:  J Thorac Dis       Date:  2014-12       Impact factor: 2.895

4.  IgG4-Related Disease: Clinical and Laboratory Features in One Hundred Twenty-Five Patients.

Authors:  Zachary S Wallace; Vikram Deshpande; Hamid Mattoo; Vinay S Mahajan; Maria Kulikova; Shiv Pillai; John H Stone
Journal:  Arthritis Rheumatol       Date:  2015-09       Impact factor: 10.995

Review 5.  Three cases of IgG4-related orbital inflammation presented as unilateral pseudotumor and review of the literature.

Authors:  Tomoki Origuchi; Hiroki Yano; Hideki Nakamura; Akiyoshi Hirano; Atsushi Kawakami
Journal:  Rheumatol Int       Date:  2012-11-09       Impact factor: 2.631

Review 6.  Immunoglobulin G4-related diseases in the head and neck: a systematic review.

Authors:  Graeme B Mulholland; Caroline C Jeffery; Paras Satija; David W J Côté
Journal:  J Otolaryngol Head Neck Surg       Date:  2015-06-20

7.  Orbital Pseudotumor: Uncommon Initial Presentation of IgG4-Related Disease.

Authors:  Teresa Carbone; Ricardo Azêdo Montes; Beatriz Andrade; Pedro Lanzieri; Luis Mocarzel
Journal:  Case Rep Rheumatol       Date:  2015-03-09

8.  IgG4- related disease: an orphan disease with many faces.

Authors:  Herwig Pieringer; Ilse Parzer; Adelheid Wöhrer; Petra Reis; Bastian Oppl; Jochen Zwerina
Journal:  Orphanet J Rare Dis       Date:  2014-07-16       Impact factor: 4.123

9.  Clinical research on benign lymphoepithelial lesions of lacrimal gland in 20 Chinese patients.

Authors:  Jian-Min Ma; Jing Li; Xin Ge; Ming Li; Jin-Ru Li; Xiao-Na Wang
Journal:  Chin Med J (Engl)       Date:  2015-02-20       Impact factor: 2.628

10.  IgG4-related disease coexisting with autoimmune haemolytic anaemia.

Authors:  Kai-Chun Wang; Hsien-Tzung Liao; Chang-Youh Tsai
Journal:  BMJ Case Rep       Date:  2018-07-06
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