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Quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy
BACKGROUND: Facial deformation as a sequela of leprosy is caused not only by a saddle nose but also by regression of the maxilla, as well documented in paleopathological observations of excavated skeletal remains of patients with leprosy. However, maxillary changes in living patients have been evalu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862504/ https://www.ncbi.nlm.nih.gov/pubmed/29522533 http://dx.doi.org/10.1371/journal.pntd.0006341 |
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author | Kasai, Norio Kondo, Osamu Suzuki, Koichi Aoki, Yoshinori Ishii, Norihisa Goto, Masamichi |
author_facet | Kasai, Norio Kondo, Osamu Suzuki, Koichi Aoki, Yoshinori Ishii, Norihisa Goto, Masamichi |
author_sort | Kasai, Norio |
collection | PubMed |
description | BACKGROUND: Facial deformation as a sequela of leprosy is caused not only by a saddle nose but also by regression of the maxilla, as well documented in paleopathological observations of excavated skeletal remains of patients with leprosy. However, maxillary changes in living patients have been evaluated only by the subjective visual grading. Here, we attempted to evaluate maxillary bone deformation in patients with leprosy using three-dimensional computed tomography (3D-CT). METHODS: Three-dimensional images centered on the maxilla were reconstructed using multiplanar reconstruction methods in former patients with leprosy (n = 10) and control subjects (n = 5); the anterior-posterior length of the maxilla (M(A-P)) was then measured. The difference between the M(A-P) of the patients and those of controls was evaluated after compensating for individual skull size. These findings were also compared with those from previous paleopathological studies. FINDINGS: Three former patients with lepromatous leprosy showed marked atrophy of the maxilla at the prosthion (-8.6, -11.1 and -17.9 mm) which corresponded with the visual appearance of the maxillary deformity, and these results were consistent with paleopathological findings of excavated skeletal remains. Additionally, the precise bone defects of the maxilla could be individually calculated for accurate reconstructive surgery. INTERPRETATION: We have successfully illustrated maxillary bone deformities in living patients with leprosy. This study also confirmed the maxillary regression described in paleopathological studies. |
format | Online Article Text |
id | pubmed-5862504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58625042018-03-28 Quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy Kasai, Norio Kondo, Osamu Suzuki, Koichi Aoki, Yoshinori Ishii, Norihisa Goto, Masamichi PLoS Negl Trop Dis Research Article BACKGROUND: Facial deformation as a sequela of leprosy is caused not only by a saddle nose but also by regression of the maxilla, as well documented in paleopathological observations of excavated skeletal remains of patients with leprosy. However, maxillary changes in living patients have been evaluated only by the subjective visual grading. Here, we attempted to evaluate maxillary bone deformation in patients with leprosy using three-dimensional computed tomography (3D-CT). METHODS: Three-dimensional images centered on the maxilla were reconstructed using multiplanar reconstruction methods in former patients with leprosy (n = 10) and control subjects (n = 5); the anterior-posterior length of the maxilla (M(A-P)) was then measured. The difference between the M(A-P) of the patients and those of controls was evaluated after compensating for individual skull size. These findings were also compared with those from previous paleopathological studies. FINDINGS: Three former patients with lepromatous leprosy showed marked atrophy of the maxilla at the prosthion (-8.6, -11.1 and -17.9 mm) which corresponded with the visual appearance of the maxillary deformity, and these results were consistent with paleopathological findings of excavated skeletal remains. Additionally, the precise bone defects of the maxilla could be individually calculated for accurate reconstructive surgery. INTERPRETATION: We have successfully illustrated maxillary bone deformities in living patients with leprosy. This study also confirmed the maxillary regression described in paleopathological studies. Public Library of Science 2018-03-09 /pmc/articles/PMC5862504/ /pubmed/29522533 http://dx.doi.org/10.1371/journal.pntd.0006341 Text en © 2018 Kasai et al 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 author and source are credited. |
spellingShingle | Research Article Kasai, Norio Kondo, Osamu Suzuki, Koichi Aoki, Yoshinori Ishii, Norihisa Goto, Masamichi Quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy |
title | Quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy |
title_full | Quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy |
title_fullStr | Quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy |
title_full_unstemmed | Quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy |
title_short | Quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy |
title_sort | quantitative evaluation of maxillary bone deformation by computed tomography in patients with leprosy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862504/ https://www.ncbi.nlm.nih.gov/pubmed/29522533 http://dx.doi.org/10.1371/journal.pntd.0006341 |
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