儿童泪囊异位骨化1例。

IF 1.5 Q3 OPHTHALMOLOGY
Journal of Ophthalmic & Vision Research Pub Date : 2025-07-30 eCollection Date: 2025-01-01 DOI:10.18502/jovr.v20.16581
Behzad Khademi, Mehdi Moallem, Mahsa Kohandel-Shirazi
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引用次数: 0

摘要

目的:我们报告一个在泪囊内出现异常肿块的泪漏病例。病例报告:一名九岁女孩,表现为间歇性单侧出血和泪囊炎发作,没有进一步的显著医学或手术史。CT扫描显示泪囊内有清晰的钙化组织。在外部泪囊鼻腔造口术后,从泪囊中取出形状良好的类似骨组织的坚硬组织并进行病理评估和活检。组织病理学分析显示异位骨形成伴泪囊非特异性炎症。在补充评估中没有发现潜在的原因,在一年的随访中没有发现复发。结论:1例儿童泪囊异位骨化,原因不明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Heterotopic Ossification Originating from the Lacrimal Sac of a Child: A Case Report.

Heterotopic Ossification Originating from the Lacrimal Sac of a Child: A Case Report.

Heterotopic Ossification Originating from the Lacrimal Sac of a Child: A Case Report.

Purpose: We present a case of hemolacria, which emerged as an unusual mass in the lacrimal sac.

Case report: A nine-year-old girl presented with intermittent unilateral hemolacria and episodes of dacryocystitis with no further remarkable medical or surgical history. CT scan indicated the presence of well-defined calcified tissue enclosed within the lacrimal sac. Following external dacryocystorhinostomy, well-formed firm tissue resembling bony tissue was extracted and sent for pathological evaluation, along with biopsies from the lacrimal sac. Histopathological analysis revealed heterotopic bone formation with nonspecific inflammation of the lacrimal sac. No underlying cause was discernible in the complementary assessment, and no recurrence was noted at one-year follow-up.

Conclusion: A child with hemolacria was found to have heterotopic ossification in the lacrimal sac with no discernible underlying cause.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
63
审稿时长
30 weeks
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