脉络丛乳头状瘤——病例报告
Choroid Plexus Papilloma - Case Presentation.
作者信息
Kabashi Antigona, Ahmetgjekaj Ilir
机构信息
Clinic of Radiology, University Clinical Center of Kosovo, Kosovo.
Prima Imaging Centre, Prishtinë, Kosovo.
出版信息
Curr Health Sci J. 2021 Apr-Jun;47(2):310-313. doi: 10.12865/CHSJ.47.02.24. Epub 2021 Jun 30.
AIM
Choroid plexus papilloma (CPP) according to the latest WHO classification system in 2016 are an uncommon, benign (WHO grade I) neuroepithelial intraventricular tumor derived from choroid plexus epithelium, which can occur in both the pediatric and adult population. These tumors account for approximately 1% of all brain tumor 2-6% of pediatric brain tumors and 0.5% of adult brain tumors.
CASE PRESENTATION
A 2-year-old female is presented at the Pediatrics Clinic at the University Clinical Center of Kosovo in a febrile, lethargic state and the anterior fontanelle is tense and swollen. The patient's parents indicate that symptoms such as food refusal, apathy, speechlessness and low mood were presented a week earlier.
CONCLUSION
Choroid plexus papilloma is a rare tumor without specific clinical patterns or imaging findings. In our presentation we have presented the role of symptoms in the detected and diagnostic of choroid plexus papilloma. Not every headache is a symptom of choroid plexus papilloma.
目的
根据2016年世界卫生组织最新分类系统，脉络丛乳头状瘤（CPP）是一种罕见的、良性（世界卫生组织一级）神经上皮性脑室内肿瘤，起源于脉络丛上皮，可发生于儿童和成人。这些肿瘤约占所有脑肿瘤的1%，儿童脑肿瘤的2 - 6%，成脑肿瘤的0.5%。
病例介绍
一名2岁女性患儿因发热、嗜睡就诊于科索沃大学临床中心儿科诊所，前囟紧张膨隆。患儿父母表示，一周前出现了拒食、冷漠、不语和情绪低落等症状。
结论
脉络丛乳头状瘤是一种罕见肿瘤，无特定临床模式或影像学表现。在我们的病例介绍中，展示了症状在脉络丛乳头状瘤检测和诊断中的作用。并非每例头痛都是脉络丛乳头状瘤的症状。
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