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Pineal Cyst Apoplexy: A Rare Complication of Common Entity

Pineal cysts (PCs) are often encountered as incidental findings in intracranial images. The vast majority of cysts are normally asymptomatic and clinically benign. Bleeding into the cysts, which leads to neurological symptoms and signs, is considered to be quite rare. The authors illustrate a newly...

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Detalles Bibliográficos
Autores principales: Kim, El, Kwon, Sae Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221466/
https://www.ncbi.nlm.nih.gov/pubmed/32390357
http://dx.doi.org/10.14791/btrt.2020.8.e4
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author Kim, El
Kwon, Sae Min
author_facet Kim, El
Kwon, Sae Min
author_sort Kim, El
collection PubMed
description Pineal cysts (PCs) are often encountered as incidental findings in intracranial images. The vast majority of cysts are normally asymptomatic and clinically benign. Bleeding into the cysts, which leads to neurological symptoms and signs, is considered to be quite rare. The authors illustrate a newly identified complication of PC in a 56-year-old woman who characterized by headache of sudden onset and vomiting. MRI disclosed a small hemorrhagic PC without narrowing of the cerebral aqueduct. The patient was managed conservatively without any surgical interventions, and she remained symptom-free over a period of 15-year follow-up. The description of this case adds to the limited literature on the series in which nonsurgical treatments had a role in the care for patients with PC complicated by intracystic hemorrhage.
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spelling pubmed-72214662020-05-24 Pineal Cyst Apoplexy: A Rare Complication of Common Entity Kim, El Kwon, Sae Min Brain Tumor Res Treat Case Report Pineal cysts (PCs) are often encountered as incidental findings in intracranial images. The vast majority of cysts are normally asymptomatic and clinically benign. Bleeding into the cysts, which leads to neurological symptoms and signs, is considered to be quite rare. The authors illustrate a newly identified complication of PC in a 56-year-old woman who characterized by headache of sudden onset and vomiting. MRI disclosed a small hemorrhagic PC without narrowing of the cerebral aqueduct. The patient was managed conservatively without any surgical interventions, and she remained symptom-free over a period of 15-year follow-up. The description of this case adds to the limited literature on the series in which nonsurgical treatments had a role in the care for patients with PC complicated by intracystic hemorrhage. The Korean Brain Tumor Society; The Korean Society for Neuro-Oncology; The Korean Society for Pediatric Neuro-Oncology 2020-04 2020-04-30 /pmc/articles/PMC7221466/ /pubmed/32390357 http://dx.doi.org/10.14791/btrt.2020.8.e4 Text en Copyright © 2020 The Korean Brain Tumor Society, The Korean Society for Neuro-Oncology, and The Korean Society for Pediatric Neuro-Oncology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, El
Kwon, Sae Min
Pineal Cyst Apoplexy: A Rare Complication of Common Entity
title Pineal Cyst Apoplexy: A Rare Complication of Common Entity
title_full Pineal Cyst Apoplexy: A Rare Complication of Common Entity
title_fullStr Pineal Cyst Apoplexy: A Rare Complication of Common Entity
title_full_unstemmed Pineal Cyst Apoplexy: A Rare Complication of Common Entity
title_short Pineal Cyst Apoplexy: A Rare Complication of Common Entity
title_sort pineal cyst apoplexy: a rare complication of common entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221466/
https://www.ncbi.nlm.nih.gov/pubmed/32390357
http://dx.doi.org/10.14791/btrt.2020.8.e4
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