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Spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: Case report

INTRODUCTION: Type1 Neurofibromatosis (NF1) is an autosomal dominant disorder with a great variety of clinical features. Vascular manifestations appear in less than 7%, and venous complications are extremely rare. CASE PRESENTATION: We report a case of an enormous cervical hematoma caused by bleedin...

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Autores principales: Ardhaoui, H., Halily, S., Mahtar, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021518/
https://www.ncbi.nlm.nih.gov/pubmed/32062119
http://dx.doi.org/10.1016/j.ijscr.2020.01.016
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author Ardhaoui, H.
Halily, S.
Mahtar, M.
author_facet Ardhaoui, H.
Halily, S.
Mahtar, M.
author_sort Ardhaoui, H.
collection PubMed
description INTRODUCTION: Type1 Neurofibromatosis (NF1) is an autosomal dominant disorder with a great variety of clinical features. Vascular manifestations appear in less than 7%, and venous complications are extremely rare. CASE PRESENTATION: We report a case of an enormous cervical hematoma caused by bleeding from the internal jugular vein in a NF1 patient. As the patient refused surgery, natural evolution was marked by spontaneous fistulization and drainage of the mass. DISCUSSION: Several cases of fragility of both the vessel wall and the surrounding tissue are discussed and two jugular vein aneurysms were reported. Management of such cases remains unclear and some reports describe defective hemostatic control at surgery. CONCLUSION: Surgery in NF1 vascular involvement should be considered on a case by case basis especially when the risk of iatrogenesis is high. Surgeons need to be aware of hemorrhagic risks, which could occur because of vessel friability.
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spelling pubmed-70215182020-02-20 Spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: Case report Ardhaoui, H. Halily, S. Mahtar, M. Int J Surg Case Rep Article INTRODUCTION: Type1 Neurofibromatosis (NF1) is an autosomal dominant disorder with a great variety of clinical features. Vascular manifestations appear in less than 7%, and venous complications are extremely rare. CASE PRESENTATION: We report a case of an enormous cervical hematoma caused by bleeding from the internal jugular vein in a NF1 patient. As the patient refused surgery, natural evolution was marked by spontaneous fistulization and drainage of the mass. DISCUSSION: Several cases of fragility of both the vessel wall and the surrounding tissue are discussed and two jugular vein aneurysms were reported. Management of such cases remains unclear and some reports describe defective hemostatic control at surgery. CONCLUSION: Surgery in NF1 vascular involvement should be considered on a case by case basis especially when the risk of iatrogenesis is high. Surgeons need to be aware of hemorrhagic risks, which could occur because of vessel friability. Elsevier 2020-01-23 /pmc/articles/PMC7021518/ /pubmed/32062119 http://dx.doi.org/10.1016/j.ijscr.2020.01.016 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ardhaoui, H.
Halily, S.
Mahtar, M.
Spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: Case report
title Spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: Case report
title_full Spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: Case report
title_fullStr Spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: Case report
title_full_unstemmed Spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: Case report
title_short Spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: Case report
title_sort spontaneous evolution of a massive hematoma caused by type 1 neurofibromatosis: case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021518/
https://www.ncbi.nlm.nih.gov/pubmed/32062119
http://dx.doi.org/10.1016/j.ijscr.2020.01.016
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