Chinratanapisit Sasawan, Tunsuriyawong Prayuth, Vichyanond Pakit, Visitsunthorn Nualanong, Luangwedchakarn Voravich, Jirapongsananuruk Orathai
Division of Allergy and Immunology, Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
J Med Assoc Thai. 2005 Nov;88 Suppl 8:S251-8.
Chronic rhinosinusitis (CRS) is a chronic inflammatory disorder of mucosa of the nose and the paranasal sinuses. Two major forms of CRS can be differentiated; CRS with nasal polyps (CRSwNP) and CRS without nasal polyps (CRSsNP). The pathophysiology and etiology of nasal polyps (NPs) are partly understood. IgG subclass deficiency was shown to be associated with an increased susceptibility to infections. However the association between NPs and IgG subclass deficiency has never been reported.
To report two cases of recalcitrant CRS and recurrent NPs with IgG subclass deficiency.
Two children (6 and 8 year-old boys) were referred to the Pediatric Allergy/Immunology Clinic, Siriraj Hospital due to a prolonged history of CRS and recurrent NPs. Both of them were treated with aggressive medical (topical and systemic corticosteroids, antibiotics, leukotriene antagonist, nasal irrigation) as well as surgical therapy, without significant improvement. Immunologic investigation in both patients showed that IgG, IgA, and IgM level were normal. IgG subclasses level in patient No. 1 were IgG1 1,235 (280-1120) mg/dl (79%), IgG2 235 (30-630) mg/dl (23.5%), IgG3 27.3 (40-250) mg/dl (1.74%), and IgG4 92.4 (11-620) mg/dl (5.9%). IgG subclasses level in patient No. 2 were IgG1 1,139 (280-1120) mg/dl (82.5%), IgG2 170 (30-630) mg/dl (12.3%), IgG3 5.6 (40-250) mg/dl (0.4%), IgG4 65.7 (11-620) mg/dl (4.8%). The diagnosis of CRS and recurrent NPs with IgG3 subclass deficiency in the first patient and IgG2/IgG3 subclass deficiency in the second patient were made. Patient No. 1 was given monthly IVIG therapy for the total of 7 courses and medications were gradually tapered. Currently, the patient is doing well after the cessation of IVIG therapy for 3 months. Patient No. 2 denied the IVIG treatment and was lost to follow up.
We reported two cases of recalcitrant CRS and recurrent NPs in children. Immunologic work up revealed IgG subclass deficiency. The treatment with monthly IVIG improved CRS and NPs in treated patient which brought up the possibility of association between NPs and IgG subclass deficiency. Further study on the direct role of IVIG in NPs will be needed in the future.
慢性鼻-鼻窦炎(CRS)是鼻腔和鼻窦黏膜的慢性炎症性疾病。CRS可分为两种主要类型:伴鼻息肉的CRS(CRSwNP)和不伴鼻息肉的CRS(CRSsNP)。鼻息肉(NPs)的病理生理学和病因学部分已为人所知。已表明IgG亚类缺乏与感染易感性增加有关。然而,NPs与IgG亚类缺乏之间的关联从未被报道过。
报告两例伴有IgG亚类缺乏的顽固性CRS和复发性NPs病例。
两名儿童(6岁和8岁男孩)因长期CRS病史和复发性NPs被转诊至诗里拉吉医院儿科过敏/免疫门诊。他们都接受了积极的药物治疗(局部和全身用糖皮质激素、抗生素、白三烯拮抗剂、鼻腔冲洗)以及手术治疗,但均无明显改善。对两名患者的免疫学检查显示,IgG、IgA和IgM水平正常。1号患者的IgG亚类水平为:IgG1 1235(280 - 1120)mg/dl(79%),IgG2 235(30 - 630)mg/dl(23.5%),IgG3 27.3(40 - 250)mg/dl(1.74%),IgG4 92.4(11 - 620)mg/dl(5.9%)。2号患者的IgG亚类水平为:IgG1 1139(280 - 1120)mg/dl(82.5%),IgG2 170(30 - 630)mg/dl(12.3%),IgG3 5.6(40 - 250)mg/dl(0.4%),IgG4 65.7(11 - 620)mg/dl(4.8%)。诊断为1号患者存在IgG3亚类缺乏的CRS和复发性NPs,2号患者存在IgG2/IgG3亚类缺乏。1号患者接受了总共7个疗程的每月一次静脉注射免疫球蛋白(IVIG)治疗,药物逐渐减量。目前,该患者在停止IVIG治疗3个月后情况良好。2号患者拒绝IVIG治疗且失访。
我们报告了两例儿童顽固性CRS和复发性NPs病例。免疫学检查发现IgG亚类缺乏。每月一次的IVIG治疗改善了接受治疗患者的CRS和NPs,这提示了NPs与IgG亚类缺乏之间存在关联的可能性。未来需要进一步研究IVIG在NPs中的直接作用。