视盘并发毛细血管瘤和垂体囊肿:多模态成像方法及文献回顾。

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2025-05-30 eCollection Date: 2025-01-01 DOI:10.1159/000544876
Devu Krishna Thulaseedharan, Abhishek Das, Parag K Shah, Narendran Venkatapathy
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引用次数: 0

摘要

摘要视盘血管瘤与脑垂体囊肿并存是一种罕见的临床现象。通常,视网膜毛细血管瘤或乳头旁血管瘤与VHL综合征有关。本病例强调临床表现、诊断方法和对患者护理的影响。病例介绍:我们报告一个年轻的病人,他来做眼科常规检查,偶然被诊断为视盘血管瘤。我们做了一个完整的系统检查以排除VHL综合征,在此期间,MRI出人意料地显示脑垂体囊肿。患者被转介给神经外科医生,由于无症状,建议进行观察。结论:本病例表明良好的临床检查、及时的文献记录、定期随访和适当的影像学检查有助于视盘毛细血管瘤和垂体囊肿的早期诊断。因此,本报告也显示了多模态成像在这些年轻患者中检测这些可能改变生活的疾病的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Concurrent Capillary Hemangioma of Optic Disc and Pituitary Gland Cyst: A Multimodal Imaging Approach and Review of Literature.

Introduction: Coexistence of optic disc hemangioma and pituitary gland cyst is a rare clinical scenario. Usually, a retinal capillary hemangioma or juxtapapillary hemangioma is associated with VHL syndrome. This case emphasizes the clinical presentation, diagnostic approach, and implications for patient care.

Case presentation: We report a case of a young patient, who came for a routine eye examination and got diagnosed with optic disc hemangioma incidentally. A complete systemic workup was done to rule out VHL syndrome during which MRI brain surprisingly revealed a pituitary gland cyst. The patient was referred to a neurosurgeon and observation was recommended as he was asymptomatic.

Conclusion: This case demonstrates how a good clinical examination, prompt documentation, regular follow-ups, and appropriate imaging facilitated the early diagnosis of both the optic disc capillary hemangioma and pituitary gland cyst. Consequently, this report also shows the importance of multimodal imaging in these young patients to detect these potentially life-altering conditions.

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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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