Ipsilateral Lymphatic and Venous Malformations Affecting the Midface Area.

IF 0.7 Q4 OPHTHALMOLOGY Case Reports in Ophthalmological Medicine Pub Date : 2020-09-18 eCollection Date: 2020-01-01 DOI:10.1155/2020/2845035
Şükran Bekdemir, Ahmet Kaan Gündüz, Ömür Ataoğlu
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引用次数: 2

Abstract

A 22-year-old woman presented with progressive swelling of the nasal conjunctiva in the left eye. Anterior segment examination revealed a diffuse cystic appearance to the inferonasal bulbar conjunctiva and plica semilunaris. Anterior segment swept-source optical coherence tomography (OCT) revealed clear hyporeflective spaces demarcated by hyperreflective septae in the affected conjunctiva, consistent with the diagnosis of lymphatic malformation (LM). Magnetic resonance imaging revealed a well circumscribed intraconal mass located inferonasally in the left orbit. Systemic examination revealed a lesion similar to LM on the left hard palate. The left conjunctival mass was excised subtotally. Subsequently, a transconjunctival anterior orbitotomy was performed and the left orbital mass was completely removed intact. Histopathologically, the conjunctival mass was diagnosed as LM and the orbital mass as venous malformation (VM). This case represents a rare coexistence of histopathologically proven conjunctival LM and orbital VM as well as a presumed LM of the hard palate, all 3 lesions occurring in the ipsilateral midface area.

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影响面中部的同侧淋巴和静脉畸形。
一个22岁的女性提出了进行性肿胀的鼻结膜在左眼。前节段检查显示鼻间球结膜和半月襞呈弥漫性囊状。前节段扫描源光学相干断层扫描(OCT)显示受影响结膜内清晰的低反射间隙,由高反射间隔划分,与淋巴畸形(LM)的诊断一致。磁共振成像显示在左眼眶鼻间有一个边界清楚的囊内肿块。全身检查发现左侧硬腭有类似LM的病变。左侧结膜肿块部分切除。随后行经结膜前眼窝切开术,将左侧眼窝肿块完整切除。结膜肿块病理诊断为LM,眼眶肿块为静脉畸形(VM)。本病例罕见地同时存在组织病理学证实的结膜LM和眶部VM,以及假定的硬腭LM,所有3个病变均发生在同侧正中面区。
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审稿时长
14 weeks
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