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Familial perimesencephalic subarachnoid hemorrhage: two case reports

INTRODUCTION: Non-aneurysmal spontaneous subarachnoid hemorrhage is characterized by an accumulation of a limited amount of subarachnoid hemorrhage, predominantly around the midbrain, and a lack of blood in the brain parenchyma or ventricular system. It represents 5% of all spontaneous subarachnoid...

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Autores principales: Cıkla, Ulaş, Aagaard-Kienitz, Beverly, Turski, Patrick A, Menekse, Guner, Niemann, David B, Başkaya, Mustafa K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4275759/
https://www.ncbi.nlm.nih.gov/pubmed/25416614
http://dx.doi.org/10.1186/1752-1947-8-380
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author Cıkla, Ulaş
Aagaard-Kienitz, Beverly
Turski, Patrick A
Menekse, Guner
Niemann, David B
Başkaya, Mustafa K
author_facet Cıkla, Ulaş
Aagaard-Kienitz, Beverly
Turski, Patrick A
Menekse, Guner
Niemann, David B
Başkaya, Mustafa K
author_sort Cıkla, Ulaş
collection PubMed
description INTRODUCTION: Non-aneurysmal spontaneous subarachnoid hemorrhage is characterized by an accumulation of a limited amount of subarachnoid hemorrhage, predominantly around the midbrain, and a lack of blood in the brain parenchyma or ventricular system. It represents 5% of all spontaneous subarachnoid hemorrhage cases. In spite of extensive investigation, understanding of the mechanisms leading to perimesencephalic non-aneurysmal subarachnoid hemorrhage remains incompletely defined. A growing body of evidence has supported a familial predisposition for non-aneurysmal spontaneous subarachnoid hemorrhage. CASE PRESENTATION: A 39-year-old Caucasian man presented with sudden onset headache associated with diplopia. His computed tomography scan revealed perimesencephalic subarachnoid hemorrhage. A cerebral angiogram showed no apparent source of bleeding. He was treated conservatively and discharged after 1 week without any neurological deficits. The older brother of the first case, a 44-year-old Caucasian man, presented 1.5 years later with acute onset of headache and his computed tomography scan also showed perimesencephalic non-aneurysmal subarachnoid hemorrhage. He was discharged home with normal neurological examination 1 week later. Follow-up angiograms did not reveal any source of bleeding in either patient. CONCLUSIONS: We report the cases of two siblings with perimesencephalic non-aneurysmal subarachnoid hemorrhage, which may further suggest a familial predisposition of non-aneurysmal spontaneous subarachnoid hemorrhage and may also point out the possible higher risk of perimesencephalic non-aneurysmal subarachnoid hemorrhage in the first-degree relatives of patients with perimesencephalic non-aneurysmal subarachnoid hemorrhage.
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spelling pubmed-42757592014-12-25 Familial perimesencephalic subarachnoid hemorrhage: two case reports Cıkla, Ulaş Aagaard-Kienitz, Beverly Turski, Patrick A Menekse, Guner Niemann, David B Başkaya, Mustafa K J Med Case Rep Case Report INTRODUCTION: Non-aneurysmal spontaneous subarachnoid hemorrhage is characterized by an accumulation of a limited amount of subarachnoid hemorrhage, predominantly around the midbrain, and a lack of blood in the brain parenchyma or ventricular system. It represents 5% of all spontaneous subarachnoid hemorrhage cases. In spite of extensive investigation, understanding of the mechanisms leading to perimesencephalic non-aneurysmal subarachnoid hemorrhage remains incompletely defined. A growing body of evidence has supported a familial predisposition for non-aneurysmal spontaneous subarachnoid hemorrhage. CASE PRESENTATION: A 39-year-old Caucasian man presented with sudden onset headache associated with diplopia. His computed tomography scan revealed perimesencephalic subarachnoid hemorrhage. A cerebral angiogram showed no apparent source of bleeding. He was treated conservatively and discharged after 1 week without any neurological deficits. The older brother of the first case, a 44-year-old Caucasian man, presented 1.5 years later with acute onset of headache and his computed tomography scan also showed perimesencephalic non-aneurysmal subarachnoid hemorrhage. He was discharged home with normal neurological examination 1 week later. Follow-up angiograms did not reveal any source of bleeding in either patient. CONCLUSIONS: We report the cases of two siblings with perimesencephalic non-aneurysmal subarachnoid hemorrhage, which may further suggest a familial predisposition of non-aneurysmal spontaneous subarachnoid hemorrhage and may also point out the possible higher risk of perimesencephalic non-aneurysmal subarachnoid hemorrhage in the first-degree relatives of patients with perimesencephalic non-aneurysmal subarachnoid hemorrhage. BioMed Central 2014-11-22 /pmc/articles/PMC4275759/ /pubmed/25416614 http://dx.doi.org/10.1186/1752-1947-8-380 Text en Copyright © 2014 Cıkla et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Cıkla, Ulaş
Aagaard-Kienitz, Beverly
Turski, Patrick A
Menekse, Guner
Niemann, David B
Başkaya, Mustafa K
Familial perimesencephalic subarachnoid hemorrhage: two case reports
title Familial perimesencephalic subarachnoid hemorrhage: two case reports
title_full Familial perimesencephalic subarachnoid hemorrhage: two case reports
title_fullStr Familial perimesencephalic subarachnoid hemorrhage: two case reports
title_full_unstemmed Familial perimesencephalic subarachnoid hemorrhage: two case reports
title_short Familial perimesencephalic subarachnoid hemorrhage: two case reports
title_sort familial perimesencephalic subarachnoid hemorrhage: two case reports
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4275759/
https://www.ncbi.nlm.nih.gov/pubmed/25416614
http://dx.doi.org/10.1186/1752-1947-8-380
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