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Complex single step skull reconstruction in Gorham’s disease - a technical report and review of the literature
BACKGROUND: Gorham’s disease is a rare osteolytic disorder characterized by progressive resorption of bone and replacement of osseous matrix by a proliferative non-neoplastic vascular or lymphatic tissue. A standardized treatment protocol has not yet been defined due to the unpredictable natural his...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365769/ https://www.ncbi.nlm.nih.gov/pubmed/25880917 http://dx.doi.org/10.1186/s12893-015-0014-4 |
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author | Ohla, Victoria Bayoumi, Ahmed B Hefty, Markus Anderson, Matthew Kasper, Ekkehard M |
author_facet | Ohla, Victoria Bayoumi, Ahmed B Hefty, Markus Anderson, Matthew Kasper, Ekkehard M |
author_sort | Ohla, Victoria |
collection | PubMed |
description | BACKGROUND: Gorham’s disease is a rare osteolytic disorder characterized by progressive resorption of bone and replacement of osseous matrix by a proliferative non-neoplastic vascular or lymphatic tissue. A standardized treatment protocol has not yet been defined due to the unpredictable natural history of the disease and variable clinical presentations. No single treatment has proven to be superior in arresting the course of the disease. Trials have included surgery, radiation and medical therapies using drugs such as calcium salts, vitamin D supplements and hormones. We report on our advantageous experience in the management of this osteolyic disorder in a case when it affected only the skull vault. A brief review of pertinent literature about Gorham’s disease with skull involvement is provided. CASE PRESENTATION: A 25-year-old Caucasian male presented with a skull depression over the left fronto-temporal region. He noticed progressive enlargement of the skull defect associated with local pain and mild headache. Physical examination revealed a tender palpable depression of the fronto-temporal convexity. Conventional X-ray of the skull showed widespread loss of bone substance. Subsequent CT scans showed features of patchy erosions indicative of an underlying osteolysis. MRI also revealed marginal enhancement at the site of the defect. The patient was in need of a pathological diagnosis as well as complex reconstruction of the afflicted area. A density graded CT scan was done to determine the variable degrees of osteolysis and a custom made allograft was designed for cranioplasty preoperatively to allow for a single step excisional craniectomy with synchronous skull repair. Gorham’s disease was diagnosed based on histopathological examination. No neurological deficit or wound complications were reported postoperatively. Over a two-year follow up period, the patient had no evidence of local recurrence or other systemic involvement. CONCLUSIONS: A single step excisional craniectomy and cranioplasty can be an effective treatment for patients with Gorham’s disease affecting the skull vault only. Preoperative planning by a density graded CT aids to design a synthetic bone flap and is beneficial in skull reconstruction. Systemic involvement is variable in this patient’s population. |
format | Online Article Text |
id | pubmed-4365769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43657692015-03-20 Complex single step skull reconstruction in Gorham’s disease - a technical report and review of the literature Ohla, Victoria Bayoumi, Ahmed B Hefty, Markus Anderson, Matthew Kasper, Ekkehard M BMC Surg Case Report BACKGROUND: Gorham’s disease is a rare osteolytic disorder characterized by progressive resorption of bone and replacement of osseous matrix by a proliferative non-neoplastic vascular or lymphatic tissue. A standardized treatment protocol has not yet been defined due to the unpredictable natural history of the disease and variable clinical presentations. No single treatment has proven to be superior in arresting the course of the disease. Trials have included surgery, radiation and medical therapies using drugs such as calcium salts, vitamin D supplements and hormones. We report on our advantageous experience in the management of this osteolyic disorder in a case when it affected only the skull vault. A brief review of pertinent literature about Gorham’s disease with skull involvement is provided. CASE PRESENTATION: A 25-year-old Caucasian male presented with a skull depression over the left fronto-temporal region. He noticed progressive enlargement of the skull defect associated with local pain and mild headache. Physical examination revealed a tender palpable depression of the fronto-temporal convexity. Conventional X-ray of the skull showed widespread loss of bone substance. Subsequent CT scans showed features of patchy erosions indicative of an underlying osteolysis. MRI also revealed marginal enhancement at the site of the defect. The patient was in need of a pathological diagnosis as well as complex reconstruction of the afflicted area. A density graded CT scan was done to determine the variable degrees of osteolysis and a custom made allograft was designed for cranioplasty preoperatively to allow for a single step excisional craniectomy with synchronous skull repair. Gorham’s disease was diagnosed based on histopathological examination. No neurological deficit or wound complications were reported postoperatively. Over a two-year follow up period, the patient had no evidence of local recurrence or other systemic involvement. CONCLUSIONS: A single step excisional craniectomy and cranioplasty can be an effective treatment for patients with Gorham’s disease affecting the skull vault only. Preoperative planning by a density graded CT aids to design a synthetic bone flap and is beneficial in skull reconstruction. Systemic involvement is variable in this patient’s population. BioMed Central 2015-03-11 /pmc/articles/PMC4365769/ /pubmed/25880917 http://dx.doi.org/10.1186/s12893-015-0014-4 Text en © Ohla et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. 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 Ohla, Victoria Bayoumi, Ahmed B Hefty, Markus Anderson, Matthew Kasper, Ekkehard M Complex single step skull reconstruction in Gorham’s disease - a technical report and review of the literature |
title | Complex single step skull reconstruction in Gorham’s disease - a technical report and review of the literature |
title_full | Complex single step skull reconstruction in Gorham’s disease - a technical report and review of the literature |
title_fullStr | Complex single step skull reconstruction in Gorham’s disease - a technical report and review of the literature |
title_full_unstemmed | Complex single step skull reconstruction in Gorham’s disease - a technical report and review of the literature |
title_short | Complex single step skull reconstruction in Gorham’s disease - a technical report and review of the literature |
title_sort | complex single step skull reconstruction in gorham’s disease - a technical report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365769/ https://www.ncbi.nlm.nih.gov/pubmed/25880917 http://dx.doi.org/10.1186/s12893-015-0014-4 |
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