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Rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review
Cavernous malformations are benign vascular malformations. Giant cavernous malformations are very rare. All reported cases have been symptomatic because of the large size and compression of the surrounding brain tissue. We report two asymptomatic cases of giant cavernous malformation that were both...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739106/ https://www.ncbi.nlm.nih.gov/pubmed/33307903 http://dx.doi.org/10.1177/0300060520926371 |
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author | Wang, Zhen Hu, Junwen Wang, Chun |
author_facet | Wang, Zhen Hu, Junwen Wang, Chun |
author_sort | Wang, Zhen |
collection | PubMed |
description | Cavernous malformations are benign vascular malformations. Giant cavernous malformations are very rare. All reported cases have been symptomatic because of the large size and compression of the surrounding brain tissue. We report two asymptomatic cases of giant cavernous malformation that were both misdiagnosed as neoplasms because of their atypical presentations. The first case was a 54-year-old man whose computed tomography and magnetic resonance imaging scans revealed an inhomogeneous lesion of 6 cm diameter and mild enhancement in the left frontal lobe. A left lateral supraorbital and transcortical approach was applied and the lesion was completely removed. The second case was a 36-year-old man with an irregular large mass in the parasellar region. Craniopharyngioma was suspected and gross total resection was performed. Post-surgical pathological analyses confirmed the diagnoses as cavernous malformations. Both patients recovered uneventfully. The rare asymptomatic giant cavernous malformations reported here in adults had benign behavior for this specific disease entity. The different clinical characteristics of ordinary cavernous malformation and adult and pediatric giant cavernous malformation imply complex and distinct genetic backgrounds. Concerns should be raised when considering giant cavernous malformation as a differential diagnosis for atypical large lesions. Surgical resection is recommended as the primary treatment option. |
format | Online Article Text |
id | pubmed-7739106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-77391062021-01-04 Rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review Wang, Zhen Hu, Junwen Wang, Chun J Int Med Res Case Report Cavernous malformations are benign vascular malformations. Giant cavernous malformations are very rare. All reported cases have been symptomatic because of the large size and compression of the surrounding brain tissue. We report two asymptomatic cases of giant cavernous malformation that were both misdiagnosed as neoplasms because of their atypical presentations. The first case was a 54-year-old man whose computed tomography and magnetic resonance imaging scans revealed an inhomogeneous lesion of 6 cm diameter and mild enhancement in the left frontal lobe. A left lateral supraorbital and transcortical approach was applied and the lesion was completely removed. The second case was a 36-year-old man with an irregular large mass in the parasellar region. Craniopharyngioma was suspected and gross total resection was performed. Post-surgical pathological analyses confirmed the diagnoses as cavernous malformations. Both patients recovered uneventfully. The rare asymptomatic giant cavernous malformations reported here in adults had benign behavior for this specific disease entity. The different clinical characteristics of ordinary cavernous malformation and adult and pediatric giant cavernous malformation imply complex and distinct genetic backgrounds. Concerns should be raised when considering giant cavernous malformation as a differential diagnosis for atypical large lesions. Surgical resection is recommended as the primary treatment option. SAGE Publications 2020-12-13 /pmc/articles/PMC7739106/ /pubmed/33307903 http://dx.doi.org/10.1177/0300060520926371 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Wang, Zhen Hu, Junwen Wang, Chun Rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review |
title | Rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review |
title_full | Rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review |
title_fullStr | Rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review |
title_full_unstemmed | Rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review |
title_short | Rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review |
title_sort | rare asymptomatic giant cerebral cavernous malformation in adults: two case reports and a literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739106/ https://www.ncbi.nlm.nih.gov/pubmed/33307903 http://dx.doi.org/10.1177/0300060520926371 |
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