Al-Mujaini Abdullah, Wali Upender, Ganesh Anuradha, Al-Hadabi Ibrahim, Burney Ikram
Department of Ophthalmology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Sultanate of Oman.
Middle East Afr J Ophthalmol. 2012 Oct;19(4):406-9. doi: 10.4103/0974-9233.102760.
To describe the clinical and histopathological features of ocular reactive lymphoid hyperplasia in children, and review the literature regarding this entity.
In this retrospective, interventional case series, a chart review was performed of three patients diagnosed with reactive lymphoid hyperplasia. Details of clinical presentation, ocular and systemic examination findings, management and subsequent course were noted.
Three children, aged 9-14 years presented with ocular adnexal masses (two unilateral and one bilateral) with 7-12 months duration. Ocular examination revealed discrete nasal conjunctival masses in two patients, and bilateral eyelid fullness and conjunctival chemosis in the third patient. Systemic evaluation and laboratory tests were normal in all patients. Orbital imaging showed lacrimal gland enlargement in one patient. Histopathological evaluation with immunohistochemical markers established the diagnosis of reactive lymphoid hyperplasia. Two patients underwent surgical excision with complete resolution. All patients have remained stable and at their last follow-up have showed no evidence of recurrence, transformation, or systemic involvement.
Reactive lymphoid hyperplasia, though uncommon in children, can have a favorable outcome with timely intervention.
描述儿童眼部反应性淋巴组织增生的临床和组织病理学特征,并回顾关于该实体的文献。
在这个回顾性、干预性病例系列中,对三名被诊断为反应性淋巴组织增生的患者进行了病历回顾。记录了临床表现、眼部和全身检查结果、治疗及后续病程的详细情况。
三名年龄在9至14岁的儿童出现眼附属器肿块(两名单侧,一名双侧),病程为7至12个月。眼部检查发现两名患者有孤立的鼻侧结膜肿块,第三名患者有双侧眼睑饱满和结膜水肿。所有患者的全身评估和实验室检查均正常。眼眶成像显示一名患者泪腺肿大。使用免疫组化标记物进行的组织病理学评估确诊为反应性淋巴组织增生。两名患者接受了手术切除,症状完全缓解。所有患者病情保持稳定,在最后一次随访时均未显示复发、转变或全身受累的迹象。
反应性淋巴组织增生在儿童中虽不常见,但及时干预可取得良好预后。