{"title":"The hidden dangers: Delayed fatal apoplexy in adult-onset optic pathway glioma following biopsy","authors":"Dawit Workneh Gechu , Mehari Wale Alem , Abel Gizaw Woldegabriel , Yordanos Girma Legesse , Mieraf Bayouh Alemu , Peniel Zewdie Abera","doi":"10.1016/j.inat.2025.102136","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Optic pathway gliomas (OPG) are the most common primary neoplasm of the optic pathway. They are most commonly seen in children less than 8 years of age. Adult onsets OPG are rare entity. Hemorrhage (Apoplexy) in these tumors is rare and it is extremely rare to occur late after a biopsy.</div></div><div><h3>Case presentation</h3><div>We describe a 33 years old right handed male patient presented with status epilepticus and right side motor preference of 5 h duration. He was on 3rd month post operation after Craniotomy and open biopsy was taken for a suspected OPG. Imaging showed massive intatumoral hemorrhage with no evident vascular abnormalities. The initial Pathology report showed pilocytic astrocytoma (PCA). He underwent Craniotomy and hematoma evacuation with right side Kochers point external ventricular drain (EVD). He had significant initial neurologic improvement but on 5th post-operative day (POD) he had re-bleeding with a fatal outcome.</div></div><div><h3>Discussion</h3><div>Apoplexy in optic pathway and hypothalamic gliomas is a rare event. While some risk factors for tumor apoplexy in optic pathway gliomas have been identified, the potential for a biopsy to precipitate delayed bleeding merits cautious consideration. Ultimately, clinical management strategies for these delicate lesions must be individually tailored, weighing the diagnostic yield against the potential for procedural complication.</div></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"42 ","pages":"Article 102136"},"PeriodicalIF":0.5000,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214751925001483","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
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Abstract
Background
Optic pathway gliomas (OPG) are the most common primary neoplasm of the optic pathway. They are most commonly seen in children less than 8 years of age. Adult onsets OPG are rare entity. Hemorrhage (Apoplexy) in these tumors is rare and it is extremely rare to occur late after a biopsy.
Case presentation
We describe a 33 years old right handed male patient presented with status epilepticus and right side motor preference of 5 h duration. He was on 3rd month post operation after Craniotomy and open biopsy was taken for a suspected OPG. Imaging showed massive intatumoral hemorrhage with no evident vascular abnormalities. The initial Pathology report showed pilocytic astrocytoma (PCA). He underwent Craniotomy and hematoma evacuation with right side Kochers point external ventricular drain (EVD). He had significant initial neurologic improvement but on 5th post-operative day (POD) he had re-bleeding with a fatal outcome.
Discussion
Apoplexy in optic pathway and hypothalamic gliomas is a rare event. While some risk factors for tumor apoplexy in optic pathway gliomas have been identified, the potential for a biopsy to precipitate delayed bleeding merits cautious consideration. Ultimately, clinical management strategies for these delicate lesions must be individually tailored, weighing the diagnostic yield against the potential for procedural complication.