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Pineal cyst apoplexy and memory loss: a novel complication

An 8-year-old boy presented to our hospital complaining of a bilateral headache associated with episodes of anterograde amnesia. He had a road traffic accident 3 years ago when a computed tomography (CT) scan revealed traumatic brain injury. In addition, a small pineal cyst (PC) was noted with minor...

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Autores principales: Shafqat, Areez, AlGethami, Hanin Jaber, Shafqat, Shameel, Islam, Syed Shafqat Ul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363962/
https://www.ncbi.nlm.nih.gov/pubmed/35965931
http://dx.doi.org/10.1016/j.radcr.2022.07.055
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author Shafqat, Areez
AlGethami, Hanin Jaber
Shafqat, Shameel
Islam, Syed Shafqat Ul
author_facet Shafqat, Areez
AlGethami, Hanin Jaber
Shafqat, Shameel
Islam, Syed Shafqat Ul
author_sort Shafqat, Areez
collection PubMed
description An 8-year-old boy presented to our hospital complaining of a bilateral headache associated with episodes of anterograde amnesia. He had a road traffic accident 3 years ago when a computed tomography (CT) scan revealed traumatic brain injury. In addition, a small pineal cyst (PC) was noted with minor intramural calcifications. A follow-up CT a day later demonstrated increased density in the pineal gland of 60 Hounsfield Units, suggestive of apoplectic changes in the PC. However, the patient was lost to follow-up and presented with memory loss a year and a half later, upon which CT and magnetic resonance imaging revealed enlargement of the PC. PC apoplexy is a very rare occurrence usually affecting young adult women; cases in children are rarely reported. Furthermore, PC apoplexy secondary to severe craniofacial trauma manifesting as memory loss has not yet been reported in the literature to the best of our knowledge.
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spelling pubmed-93639622022-08-11 Pineal cyst apoplexy and memory loss: a novel complication Shafqat, Areez AlGethami, Hanin Jaber Shafqat, Shameel Islam, Syed Shafqat Ul Radiol Case Rep Case Report An 8-year-old boy presented to our hospital complaining of a bilateral headache associated with episodes of anterograde amnesia. He had a road traffic accident 3 years ago when a computed tomography (CT) scan revealed traumatic brain injury. In addition, a small pineal cyst (PC) was noted with minor intramural calcifications. A follow-up CT a day later demonstrated increased density in the pineal gland of 60 Hounsfield Units, suggestive of apoplectic changes in the PC. However, the patient was lost to follow-up and presented with memory loss a year and a half later, upon which CT and magnetic resonance imaging revealed enlargement of the PC. PC apoplexy is a very rare occurrence usually affecting young adult women; cases in children are rarely reported. Furthermore, PC apoplexy secondary to severe craniofacial trauma manifesting as memory loss has not yet been reported in the literature to the best of our knowledge. Elsevier 2022-08-05 /pmc/articles/PMC9363962/ /pubmed/35965931 http://dx.doi.org/10.1016/j.radcr.2022.07.055 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Shafqat, Areez
AlGethami, Hanin Jaber
Shafqat, Shameel
Islam, Syed Shafqat Ul
Pineal cyst apoplexy and memory loss: a novel complication
title Pineal cyst apoplexy and memory loss: a novel complication
title_full Pineal cyst apoplexy and memory loss: a novel complication
title_fullStr Pineal cyst apoplexy and memory loss: a novel complication
title_full_unstemmed Pineal cyst apoplexy and memory loss: a novel complication
title_short Pineal cyst apoplexy and memory loss: a novel complication
title_sort pineal cyst apoplexy and memory loss: a novel complication
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363962/
https://www.ncbi.nlm.nih.gov/pubmed/35965931
http://dx.doi.org/10.1016/j.radcr.2022.07.055
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