Eslami Maryam, Rossman David, Rasmussen Steve, Chae Tony
Department of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, Canada.
Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
Am J Ophthalmol Case Rep. 2022 Feb 4;25:101341. doi: 10.1016/j.ajoc.2022.101341. eCollection 2022 Mar.
To add to the existing yet limited body of knowledge around crystal-storing histiocytosis (CSH) with two case reports of localized ocular CSH and associated mucosa-associated lymphoid tissue (MALT) lymphoma involving the lacrimal and orbital soft tissues without underlying systemic lymphoproliferative disorders and to provide a literature review of all cases of CSH with associated ophthalmic findings reported to date.
A 62-year-old male presented with a one-year history of right greater than left upper eyelid swelling and epiphora. Ophthalmic exam and computed tomography (CT) head scan revealed bilateral soft tissue masses superior to the globe encasing the supraorbital artery with poor margins from the superior rectus muscle. A biopsy of the lesion showed low grade B-cell lymphoma and associated CSH with lymphoma making up the bulk of the tumor and with CSH comprising a minor component of the overall tumor volume. Further investigations did not show any evidence of systemic lymphoproliferative disorders. He received local irradiation of orbits, which resulted in complete resolution of disease.An 85-year-old female with no significant past ocular history referred to ophthalmology services for an incidental finding of an enlarged left lacrimal gland on a CT head scan. Ophthalmic exam and subsequent magnetic resonance imaging (MRI) demonstrated an enlarged left lacrimal gland. A biopsy of the lesion showed MALT lymphoma associated with CSH. In this case, CSH comprised the bulk of the clinical mass rather than lymphoma. Following negative systemic investigations, she received a short course of localized radiotherapy with a 50% regression of disease seen on follow-up CT scan.
These two cases demonstrate a spectrum of morphology associated with CSH. In addition, they show that although localized ocular CSH is rare, CSH should be considered in the differential of an orbital mass and should lead to consideration of further investigation for systemic lymphoproliferative disorders.
通过两例局限性眼部晶体储存性组织细胞增多症(CSH)及相关黏膜相关淋巴组织(MALT)淋巴瘤累及泪腺和眼眶软组织且无潜在系统性淋巴增殖性疾病的病例报告,补充围绕CSH的现有但有限的知识体系,并对迄今报道的所有伴有眼科表现的CSH病例进行文献综述。
一名62岁男性,有右眼上睑肿胀大于左眼且溢泪1年的病史。眼科检查和头颅计算机断层扫描(CT)显示双侧眼球上方软组织肿块,包绕眶上动脉,与上直肌边界不清。病变活检显示低级别B细胞淋巴瘤及相关CSH,淋巴瘤构成肿瘤主体,CSH占肿瘤总体积的一小部分。进一步检查未发现系统性淋巴增殖性疾病的任何证据。他接受了眼眶局部放疗,疾病完全缓解。
一名85岁女性,既往无明显眼部病史,因头颅CT偶然发现左泪腺肿大而转诊至眼科。眼科检查及随后的磁共振成像(MRI)显示左泪腺肿大。病变活检显示与CSH相关的MALT淋巴瘤。在该病例中,CSH构成临床肿块的主体而非淋巴瘤。全身检查阴性后,她接受了短疗程局部放疗,随访CT扫描显示疾病消退50%。
这两例病例展示了与CSH相关的一系列形态学表现。此外,它们表明尽管局限性眼部CSH罕见,但在眼眶肿块的鉴别诊断中应考虑CSH,并应促使考虑对系统性淋巴增殖性疾病进行进一步检查。