GradP - o53 Síndrome de Sturge-Weber: relato de caso Article Swipe

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Lara Mariano Pinheiro , Gabriel Mulinari‐Santos , Ciro Borges Duailibe de Deus , Lara Ribeiro Feitosa Duailibe , João Paulo Bonardi , Leonardo Pérez Faverani ·

YOU? · · 2016 · Open Access ·

A Sindrome de Sturge-Weber e definida como uma doenca extrememente rara, congenita mas nao hereditaria, e que envolve proliferacoes vasculares harmatomatosas neurologicas e dermatologicas. Caracterizada por angiomatose corticocerebral, calcificacoes cerebrais, crises epilepticas, alteracoes visuais, retardo mental e a presenca do nevo flamineo ou mancha do vinho do porto, que progrede pelo trajeto do nervo trigemio, sendo bastante sugestivo dessa afeccao. Paciente F. H. O. de 26 anos de idade, portador da sindrome de Sturge-Weber comparece ao ambulatorio da Cirurgia e Traumatologia Bucomaxilofacial com indicacao para extracao dos elementos (36, 37 e 38) com extensa destruicao coronaria. Apresentando ainda polipo pulpar, drenagem purulenta em regiao acometida e ampla mobilidade. O planejamento e tratamento cirurgico preconizado foi remocao dos elementos citados. O paciente foi operado em âmbito hospitalar sob anestesia local, todos os cuidados hemostaticos foram realizados a fim de se evitar a intensa hemorragia que pode ser encontrada nesses casos. A Sindrome de Sturge-Weber deve ser sempre corretamente diagnosticada devido a presenca de lesoes hemangiomatosas, para que haja um detalhado planejamento cirurgico, a fim de evitar desordens hemorragicas, que podem se tornar uma complicacao significante durante o ato cirurgico. Descritores: Sindrome de Sturge-Weber, Hemostasia, Patologia Oral.

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Type: article
Language: es
Landing Page: http://www.archhealthinvestigation.com.br/index.php/ArcHI/article/view/1620/pdf
OA Status: green
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Title: GradP - o53 Síndrome de Sturge-Weber: relato de caso

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Language: es

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Publication year: 2016

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Publication date: 2016-08-04

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Authors: Lara Mariano Pinheiro, Gabriel Mulinari‐Santos, Ciro Borges Duailibe de Deus, Lara Ribeiro Feitosa Duailibe, João Paulo Bonardi, Leonardo Pérez Faverani

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Landing page: https://www.archhealthinvestigation.com.br/index.php/ArcHI/article/view/1620/pdf

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