Beykin Gala, Pe'er Jacob, Amir Gail, Frenkel Shahar
Department of Ophthalmology, Hadassah-Hebrew University Medical Center, , Jerusalem, Israel.
Br J Ophthalmol. 2014 May;98(5):645-50. doi: 10.1136/bjophthalmol-2013-303527. Epub 2013 Oct 25.
To report clinical, histopathological and molecular features of 'salmon patch'-like conjunctival lesions in paediatric and adolescent patients, and discuss management of these patients and outcome.
Patients who presented between 2000 and 2011 with a conjunctival 'salmon-patch'-like lesion in the plical area, were identified by chart review. Clinical parameters, demographic characteristics and details of ophthalmic imaging were collected, and the effect of treatment examined.
Eleven patients aged 6-21 years, presented with an elevated pink conjunctival mass in the plical area of one or both eyes. Nine patients underwent an excisional biopsy that histopathologically disclosed extranodal marginal zone B cell lymphoma of mucosa-associated lymphoid tissue (also termed 'MALT lymphoma') in two cases and reactive lymphoid hyperplasia (RLH) in seven cases. Molecular diagnosis showed polyclonal B cells in six patients, monoclonal B cells in two patients, and a questionable status in one patient. Systemic examination disclosed localised ocular adnexal disease in the patients with MALT lymphoma, and none had either local or systemic recurrence during follow-up. Two other patients were treated with antiallergic medication with resolution of the lesion, and were therefore diagnosed clinically with RLH.
It is clinically difficult to differentiate between conjunctival RLH and MALT lymphoma in the paediatric and adolescent population. Both lesions are rare in this age group, particularly MALT lymphoma. Molecular analysis of excised lesions does not always correlate with histopathology. A short treatment course with antiallergic drops may sometimes assist diagnosis without compromising the patients due to the indolent nature of lymphoma in that area.
报告儿童及青少年患者中“鲑鱼斑”样结膜病变的临床、组织病理学及分子特征,并探讨这些患者的管理及预后。
通过病历回顾确定2000年至2011年间在睑褶区出现结膜“鲑鱼斑”样病变的患者。收集临床参数、人口统计学特征及眼科影像学细节,并检查治疗效果。
11例年龄在6至21岁的患者,在一只或两只眼睛的睑褶区出现粉红色结膜肿物。9例患者接受了切除活检,组织病理学检查显示2例为黏膜相关淋巴组织结外边缘区B细胞淋巴瘤(也称为“MALT淋巴瘤”),7例为反应性淋巴样增生(RLH)。分子诊断显示6例患者为多克隆B细胞,2例患者为单克隆B细胞,1例患者情况可疑。全身检查发现MALT淋巴瘤患者存在局限性眼附属器疾病,随访期间均无局部或全身复发。另外2例患者接受抗过敏药物治疗后病变消退,因此临床诊断为RLH。
在儿童及青少年人群中,临床上难以区分结膜RLH和MALT淋巴瘤。这两种病变在该年龄组均罕见,尤其是MALT淋巴瘤。切除病变的分子分析并不总是与组织病理学相关。由于该区域淋巴瘤生长缓慢,短期使用抗过敏滴眼液治疗有时可能有助于诊断而不影响患者。