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Chemokine receptors in gastric MALT lymphoma: loss of CXCR4 and upregulation of CXCR7 is associated with progression to diffuse large B-cell lymphoma.胃黏膜相关淋巴组织淋巴瘤中的趋化因子受体:CXCR4 的丢失和 CXCR7 的上调与向弥漫性大 B 细胞淋巴瘤的进展相关。
Mod Pathol. 2013 Feb;26(2):182-94. doi: 10.1038/modpathol.2012.134. Epub 2012 Aug 31.
2
Ophthalmologic outcomes after chemotherapy and/or radiotherapy in non-conjunctival ocular adnexal MALT lymphoma.非结膜眼附属器黏膜相关淋巴组织淋巴瘤经化疗和/或放疗后的眼科结局。
Ann Hematol. 2012 Sep;91(9):1393-401. doi: 10.1007/s00277-012-1469-3. Epub 2012 Apr 29.
3
Orbital lymphoma presenting with choroidal detachments.眼眶淋巴瘤伴脉络膜脱离。
Ophthalmic Plast Reconstr Surg. 2010 Nov-Dec;26(6):479-81. doi: 10.1097/IOP.0b013e3181cff63d.
4
Spectral-domain optical coherence tomography of conjunctival mucosa-associated lymphoid tissue lymphoma with presumed choroidal involvement.伴有脉络膜累及疑似表现的结膜黏膜相关淋巴组织淋巴瘤的光谱域光学相干断层扫描。
Graefes Arch Clin Exp Ophthalmol. 2010 Dec;248(12):1837-40. doi: 10.1007/s00417-010-1427-5. Epub 2010 Jun 8.
5
Choroidal lymphoma masquerading as anterior ischemic optic neuropathy.伪装成前部缺血性视神经病变的脉络膜淋巴瘤。
Eur J Ophthalmol. 2010 Sep-Oct;20(5):959-62. doi: 10.1177/112067211002000525.
6
Uveal effusion syndrome caused by choroidal invasion of malignant lymphoma.恶性淋巴瘤脉络膜浸润引起的葡萄膜渗漏综合征。
Jpn J Ophthalmol. 2010 Jan;54(1):109-10. doi: 10.1007/s10384-009-0757-5. Epub 2010 Feb 12.
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Primary extranodal marginal zone lymphoma of the uvea associated with massive diffuse epibulbar extension and focal infiltration of the optic nerve and meninges, clinically presented as uveitis masquerade syndrome: a case report.眼葡萄膜原发性结外边缘区淋巴瘤伴弥漫性广泛眶内蔓延及视神经和脑膜局限性浸润,临床表现为伪装综合征的葡萄膜炎:一例报告。
Med Oncol. 2010 Sep;27(3):1010-6. doi: 10.1007/s12032-009-9325-6. Epub 2009 Oct 9.
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Extranodal B-cell uveal lymphoma with extraocular involvement.伴有眼外受累的结外B细胞葡萄膜淋巴瘤。
Can J Ophthalmol. 2009 Apr;44(2):213-4. doi: 10.3129/i08-176.
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10
Intracular, pan-uveal intravascular large B-cell lymphoma associated with choroidal infarction and choroidal tri-lineage extramedullary haemtopoiesis.眼内、全葡萄膜血管内大B细胞淋巴瘤伴脉络膜梗死及脉络膜三系髓外造血。
Histopathology. 2007 Aug;51(2):275-9. doi: 10.1111/j.1365-2559.2007.02750.x. Epub 2007 Jun 25.

脉络膜和附属器官外结外边缘区 B 细胞淋巴瘤:九例系列病例的表现、影像学发现和治疗管理。

Choroidal and adnexal extranodal marginal zone B-cell lymphoma: presentation, imaging findings, and therapeutic management in a series of nine cases.

机构信息

Department of Ophthalmology, Pitié-Salpétrière Hospital, Paris, France.

出版信息

Eye (Lond). 2013 Jul;27(7):828-35. doi: 10.1038/eye.2013.74. Epub 2013 Apr 19.

DOI:10.1038/eye.2013.74
PMID:23598677
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3709394/
Abstract

PURPOSE

To describe the clinical and imaging presentation, pitfalls in the diagnosis of choroidal extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT), as well as the therapeutic management and prognosis.

METHODS

A retrospective case review of nine choroidal MALT lymphomas was performed. Initial clinical presentation and imaging findings of these histologically confirmed cases of lymphoma were analyzed. Treatment methods, time to diagnosis, systemic work-up, and treatment prognosis were assessed.

RESULTS

Initial presentation was essentially blurred vision. The features described on examination were: anterior and posterior scleritis, iridocyclitis, choroidal infiltration, and exudative retinal detachment. Fluorescein and indocyanine green angiography as well as ultrasonography and optic coherence tomography provided arguments in favor of the diagnosis. Biopsy sites included conjunctiva, Tenon's capsule, deep scleral tissue, episclera, lacrimal gland, and choroid. Treatment mostly consisted of a combination of chemotherapy and radiotherapy. The mean time to diagnosis was 12 months.

CONCLUSIONS

Owing to the insidious onset of these tumors and their ability to simulate other conditions, the diagnosis is commonly delayed. The prognosis is generally good and treatment is effective in the case of localized lymphoma.

摘要

目的

描述黏膜相关淋巴组织(MALT)结外边缘区 B 细胞淋巴瘤的眼脉络膜临床和影像学表现、诊断误区,以及治疗管理和预后。

方法

对 9 例眼脉络膜 MALT 淋巴瘤进行回顾性病例复查。分析这些经组织学证实的淋巴瘤病例的初始临床表现和影像学发现。评估治疗方法、诊断时间、全身检查以及治疗预后。

结果

最初的表现主要是视力模糊。检查中描述的特征包括:前巩膜炎、后巩膜炎、虹膜睫状体炎、脉络膜浸润和渗出性视网膜脱离。荧光素和吲哚菁绿血管造影以及超声检查和光学相干断层扫描为诊断提供了依据。活检部位包括结膜、Tenon 囊、深层巩膜组织、巩膜、泪腺和脉络膜。治疗主要包括化疗和放疗的联合应用。平均诊断时间为 12 个月。

结论

由于这些肿瘤的隐匿性发病和模拟其他疾病的能力,诊断通常会被延误。在局限性淋巴瘤的情况下,预后通常良好,治疗效果明显。