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Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome

Gorham-Stout disease (GSD) is a rare condition in which spontaneous, progressive resorption of bone occurs. There are no previous reports of patients with fatal progression of GSD with skull base osteomyelitis (SBO) and lateral medullary syndrome (LMS). We present the case of a 27-year-old man diagn...

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Autores principales: Nozawa, Akifumi, Ozeki, Michio, Hori, Tomohiro, Kato, Hiroki, Ohe, Naoyuki, Fukao, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663530/
https://www.ncbi.nlm.nih.gov/pubmed/30799352
http://dx.doi.org/10.2169/internalmedicine.2118-18
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author Nozawa, Akifumi
Ozeki, Michio
Hori, Tomohiro
Kato, Hiroki
Ohe, Naoyuki
Fukao, Toshiyuki
author_facet Nozawa, Akifumi
Ozeki, Michio
Hori, Tomohiro
Kato, Hiroki
Ohe, Naoyuki
Fukao, Toshiyuki
author_sort Nozawa, Akifumi
collection PubMed
description Gorham-Stout disease (GSD) is a rare condition in which spontaneous, progressive resorption of bone occurs. There are no previous reports of patients with fatal progression of GSD with skull base osteomyelitis (SBO) and lateral medullary syndrome (LMS). We present the case of a 27-year-old man diagnosed with GSD with involvement of the maxillofacial bones and skull base. The patient developed SBO; LMS resulted from progressive osteolysis, and the patient died of associated brainstem stroke. Careful follow-up with special emphasis on the early detection of intracranial complications is critical in patients presenting with progressive GSD with involvement of the skull base.
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spelling pubmed-66635302019-07-29 Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome Nozawa, Akifumi Ozeki, Michio Hori, Tomohiro Kato, Hiroki Ohe, Naoyuki Fukao, Toshiyuki Intern Med Case Report Gorham-Stout disease (GSD) is a rare condition in which spontaneous, progressive resorption of bone occurs. There are no previous reports of patients with fatal progression of GSD with skull base osteomyelitis (SBO) and lateral medullary syndrome (LMS). We present the case of a 27-year-old man diagnosed with GSD with involvement of the maxillofacial bones and skull base. The patient developed SBO; LMS resulted from progressive osteolysis, and the patient died of associated brainstem stroke. Careful follow-up with special emphasis on the early detection of intracranial complications is critical in patients presenting with progressive GSD with involvement of the skull base. The Japanese Society of Internal Medicine 2019-02-25 2019-07-01 /pmc/articles/PMC6663530/ /pubmed/30799352 http://dx.doi.org/10.2169/internalmedicine.2118-18 Text en Copyright © 2019 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Nozawa, Akifumi
Ozeki, Michio
Hori, Tomohiro
Kato, Hiroki
Ohe, Naoyuki
Fukao, Toshiyuki
Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome
title Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome
title_full Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome
title_fullStr Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome
title_full_unstemmed Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome
title_short Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary Syndrome
title_sort fatal progression of gorham-stout disease with skull base osteomyelitis and lateral medullary syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663530/
https://www.ncbi.nlm.nih.gov/pubmed/30799352
http://dx.doi.org/10.2169/internalmedicine.2118-18
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