Sohn Eun Jung, Ahn Hee Bae, Roh Mee Sook, Jung Woo Jun, Ryu Won Yeol, Kwon Yoon Hyung
Departments of Ophthalmology.
Pathology, Dong-A University College of Medicine, Busan, Republic of Korea.
Ophthalmic Plast Reconstr Surg. 2018 Jul/Aug;34(4):313-319. doi: 10.1097/IOP.0000000000000965.
To report clinical and pathological characteristics of idiopathic orbital inflammation and ocular adnexal mucosa-associated lymphoid tissue (MALT) lymphoma with immunoglobulin G4 (IgG4)-positive plasma cells.
A retrospective histopathological review and clinical case series. A total of 51 biopsy samples from January 2005 to December 2015 were used in this study, including 21 cases of biopsy-confirmed idiopathic orbital inflammation and 30 cases of biopsy-confirmed ocular adnexal MALT lymphoma. Most cases of ocular adnexal lymphoma were conjunctival tissue. Retrospective immunohistochemical studies were performed to estimate the IgG4 and IgG4/IgG ratios. Histopathologic features, demographic and clinical data, radiologic findings, treatment, and follow-up information for each patient were analyzed.
Among idiopathic orbital inflammation, 6 (28.6%) of the 21 patients were diagnosed as "probable" ocular adnexal IgG4-related diseases and 13 (43.3%) of the 30 patients were diagnosed as MALT lymphoma with IgG4-positive plasma cells. Six cases of 13 IgG4-positive MALT lymphoma group had contralateral chronic inflammatory lesions infiltrated by IgG4-positive plasma cells, which was significantly (p = 0.007) higher than that in the IgG4-negative group. Conjunctival involvement was 69% of the IgG4-positive MALT lymphoma cases. Bilateral involvement of the ocular adnexa was significantly (p = 0.02) more frequent among IgG4-positive MALT lymphoma patients than that in IgG4-positive idiopathic orbital inflammation patients. Recurrence rate in the IgG4-positive group was higher (p = 0.05) than that in the IgG4-negative group but not significantly.
This study presented an unusual framework of ocular adnexal IgG4-related inflammation, in conjunctiva. It is important to understand contralateral chronic inflammatory lesions and their relationship with IgG4-positive MALT lymphoma. Tissue biopsy and IgG4 immunostaining are required for all cases because IgG4-positive MALT lymphoma can arise from a pre-existing IgG4-positive chronic inflammatory lesions. This is the first study that performs IgG4 immunostaining for tissue from a relatively large number of conjunctival MALT lymphomas in a single center. Therefore, it will help to diagnose conjunctival lymphoproliferative disease.
报告特发性眼眶炎症以及伴有免疫球蛋白G4(IgG4)阳性浆细胞的眼附属器黏膜相关淋巴组织(MALT)淋巴瘤的临床和病理特征。
一项回顾性组织病理学研究及临床病例系列。本研究使用了2005年1月至2015年12月期间的51份活检样本,包括21例经活检确诊的特发性眼眶炎症病例和30例经活检确诊的眼附属器MALT淋巴瘤病例。眼附属器淋巴瘤的大多数病例为结膜组织。进行回顾性免疫组织化学研究以评估IgG4和IgG4/IgG比率。分析了每位患者的组织病理学特征、人口统计学和临床数据、影像学检查结果、治疗及随访信息。
在特发性眼眶炎症患者中,21例中有6例(28.6%)被诊断为“可能的”眼附属器IgG4相关疾病,30例中有13例(43.3%)被诊断为伴有IgG4阳性浆细胞的MALT淋巴瘤。13例IgG4阳性MALT淋巴瘤组中有6例对侧存在IgG-4阳性浆细胞浸润的慢性炎症病变,这一比例显著高于IgG4阴性组(p = 0.007)。IgG4阳性MALT淋巴瘤病例中结膜受累占69%。IgG4阳性MALT淋巴瘤患者眼附属器双侧受累的频率显著高于IgG4阳性特发性眼眶炎症患者(p = 0.02)。IgG4阳性组的复发率高于IgG4阴性组(p = 0.05),但差异不显著。
本研究展示了结膜中眼附属器IgG4相关炎症的一个不同寻常的框架。了解对侧慢性炎症病变及其与IgG4阳性MALT淋巴瘤的关系很重要。所有病例均需要进行组织活检和IgG4免疫染色,因为IgG4阳性MALT淋巴瘤可能起源于先前存在的IgG4阳性慢性炎症病变。这是第一项在单一中心对相对大量结膜MALT淋巴瘤组织进行IgG4免疫染色的研究。因此,它将有助于诊断结膜淋巴增殖性疾病。