Immunoglobulin G4 related chronic sclerosing sialadenitis

涎腺炎 医学 疾病 活检 颌下腺 抗体 病理 唾液腺 皮肤病科 重症监护医学 免疫学
作者
Emma L. Culver,A. Hunt,Evelyn Crewe,Ketan A. Shah,Pablo Martinez‐Devesa
出处
期刊:Journal of Laryngology and Otology [Cambridge University Press]
卷期号:129 (3): 226-231 被引量:14
标识
DOI:10.1017/s0022215115000195
摘要

Abstract Background: ENT surgeons may be the first specialists to encounter and diagnose patients with salivary gland disease. A new entity involving the salivary glands has recently been described of which ENT surgeons need to be aware: immunoglobulin G4 related chronic sclerosing sialadenitis. Method: A literature search of Medline, Embase and Cochrane Library databases was performed, using the search terms ‘IgG4’, ‘hyperIgG4 syndrome’ and ‘IgG4 related chronic sclerosing sialadenitis’. Results: Knowledge concerning immunoglobulin G4 related chronic sclerosing sialadenitis is rapidly increasing. This new entity is part of a fibro-inflammatory corticosteroid-responsive systemic disease (immunoglobulin G4 related disease) and has been described in almost every organ. Biopsy of the submandibular gland can be diagnostic. However, the diagnosis can easily be overlooked if: clinical suspicion is not high, one is unaware of the classical morphology and/or immunoglobulin G4 staining is not performed. This paper presents a summary of the current understanding of the disease and its management. Conclusion: ENT surgeons should be aware of this new disease entity. Patients with systemic disease should be managed under a multidisciplinary team, with input from clinicians who have an interest in such diseases (such as gastroenterologists and rheumatologists), and input from histopathologists and radiologists.
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