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两名儿科患者泪道系统的原发性黏膜相关淋巴组织(MALT)淋巴瘤。

Primary mucosa-associated lymphoid tissue (MALT) lymphoma of the lacrimal drainage system in two pediatric patients.

作者信息

Ucgul Ahmet Yucel, Tarlan Bercin, Gocun Pınar Uyar, Konuk Onur

机构信息

Department of Ophthalmology, Training and Research Hospital, Abant Izzet Baysal University, Bolu, Turkey.

Department of Ophthalmology, Gazi University Medical School, Ankara, Turkey.

出版信息

Eur J Ophthalmol. 2020 May;30(3):NP18-NP23. doi: 10.1177/1120672119837085. Epub 2019 Mar 12.

DOI:10.1177/1120672119837085
PMID:30862184
Abstract

Primary non-Hodgkin lymphoma (NHL) of lacrimal drainage system (LDS) is quite rare in children, but it is important to expedite early diagnosis in an effort to alter possible life-threatening disease since they are usually misdiagnosed as chronic dacryocystitis. In the literature, there are few examples of tumors of LDS in children. The authors herein report two pediatric cases of extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) originating from lacrimal sac in an attempt to increase the knowledge about the clinical course of NHL of LDS. Considerable care must be taken since tumors of lacrimal drainage can mimic dacryocystitis clinically and macroscopically. Two patients both attended with painless swelling in the left lacrimal sac region and epiphora of the left eye. Orbital magnetic resonance imaging showed a tumoral lesion in the left lacrimal sac region and histopathological examination of excisional biopsy specimen demonstrated MALT lymphoma in both patients. The treatment regimen comprises lacrimal sac excision within the tumor, canalicular dacryocystorhinostomy (DCR) with bicanalicular silicone intubation (BSI) combined with chemotherapy and regional radiotherapy in one case, whereas the second case received only radiotherapy after canalicular DCR with BSI. Both of them maintained clinical remission along follow-up.

摘要

泪道系统原发性非霍奇金淋巴瘤(NHL)在儿童中相当罕见,但由于其通常被误诊为慢性泪囊炎,为改变可能危及生命的疾病状况,加快早期诊断很重要。在文献中,儿童泪道系统肿瘤的例子很少。本文作者报告了两例起源于泪囊的黏膜相关淋巴组织结外边缘区淋巴瘤(MALT淋巴瘤)的儿科病例,以增加对泪道系统NHL临床病程 的了解。由于泪道肿瘤在临床和宏观上可模仿泪囊炎,必须格外小心。两名患者均因左泪囊区无痛性肿胀和左眼溢泪就诊。眼眶磁共振成像显示左泪囊区有肿瘤性病变,切除活检标本的组织病理学检查证实两名患者均为MALT淋巴瘤。治疗方案包括一例在肿瘤内切除泪囊、行双泪小管硅胶插管的泪囊鼻腔吻合术(DCR)并联合化疗和局部放疗,而第二例在双泪小管硅胶插管的泪囊鼻腔吻合术后仅接受放疗。随访期间两人均保持临床缓解。

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