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Radiotherapy in Fibrodysplasia Ossificans Progressiva: A Case Report and Systematic Review of the Literature

Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant disease, characterized by the formation of heterotopic ossification (HO) in muscles, ligaments, and tendons. Flare-ups, an inflammatory process that often precedes the formation of HO, can occur spontaneously, but trauma is also a...

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Autores principales: Botman, Esmée, Netelenbos, Jan Coen, Rustemeyer, Thomas, Schoonmade, Linda J., Nieuwenhuijzen, Jakko A., Teunissen, Bernd P., Visser, Marieke, Raijmakers, Pieter, Lammertsma, Adriaan A., Dahele, Max, Eekhoff, Marelise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028822/
https://www.ncbi.nlm.nih.gov/pubmed/32117050
http://dx.doi.org/10.3389/fendo.2020.00006
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author Botman, Esmée
Netelenbos, Jan Coen
Rustemeyer, Thomas
Schoonmade, Linda J.
Nieuwenhuijzen, Jakko A.
Teunissen, Bernd P.
Visser, Marieke
Raijmakers, Pieter
Lammertsma, Adriaan A.
Dahele, Max
Eekhoff, Marelise
author_facet Botman, Esmée
Netelenbos, Jan Coen
Rustemeyer, Thomas
Schoonmade, Linda J.
Nieuwenhuijzen, Jakko A.
Teunissen, Bernd P.
Visser, Marieke
Raijmakers, Pieter
Lammertsma, Adriaan A.
Dahele, Max
Eekhoff, Marelise
author_sort Botman, Esmée
collection PubMed
description Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant disease, characterized by the formation of heterotopic ossification (HO) in muscles, ligaments, and tendons. Flare-ups, an inflammatory process that often precedes the formation of HO, can occur spontaneously, but trauma is also a common trigger. It is not known whether radiotherapy, especially in higher doses, might cause sufficient trauma or inflammation to trigger a flare-up and subsequent HO in FOP patients. We report the case of a patient undergoing radiotherapy for the treatment of a 1-cm-wide basal cell carcinoma (BCC) of the lower lip. In addition, we present a systematic review of the available literature. Our patient received 54 Gy in 18 fractions with orthovoltage therapy, resulting in a clinical complete response of the tumor. Six months after treatment, there were no signs of HO either clinically or on [(18)F]NaF PET/CT. The systematic review identified 11 publications describing either radiation treatment in FOP or radiation therapy as a cause of HO in non-FOP patients. Six case reports described the use of radiation in FOP patients for various reasons, including one with a high-dose treatment of a lip BCC using superficial X-ray therapy. The remaining five studies described the use of low-dose radiotherapy to prevent or treat either an FOP flare-up or HO formation. None of these cases showed worsening of disease that could be attributed to the use of radiation therapy. Radiation induced HO in non-FOP patients was rare and occurred in five studies. The largest of these studies suggested that HO was induced after treatment with high doses, resulting in more widespread evidence of tissue damage, potentially being the end result of this damage. In conclusion, available reports suggest no contraindication to radiotherapy in FOP patients; although the number of cases was small, systematic toxicity reports often were not available, and none of the reports described high-dose, high-energy radiation treatment at locations such as muscle and joint regions.
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spelling pubmed-70288222020-02-28 Radiotherapy in Fibrodysplasia Ossificans Progressiva: A Case Report and Systematic Review of the Literature Botman, Esmée Netelenbos, Jan Coen Rustemeyer, Thomas Schoonmade, Linda J. Nieuwenhuijzen, Jakko A. Teunissen, Bernd P. Visser, Marieke Raijmakers, Pieter Lammertsma, Adriaan A. Dahele, Max Eekhoff, Marelise Front Endocrinol (Lausanne) Endocrinology Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant disease, characterized by the formation of heterotopic ossification (HO) in muscles, ligaments, and tendons. Flare-ups, an inflammatory process that often precedes the formation of HO, can occur spontaneously, but trauma is also a common trigger. It is not known whether radiotherapy, especially in higher doses, might cause sufficient trauma or inflammation to trigger a flare-up and subsequent HO in FOP patients. We report the case of a patient undergoing radiotherapy for the treatment of a 1-cm-wide basal cell carcinoma (BCC) of the lower lip. In addition, we present a systematic review of the available literature. Our patient received 54 Gy in 18 fractions with orthovoltage therapy, resulting in a clinical complete response of the tumor. Six months after treatment, there were no signs of HO either clinically or on [(18)F]NaF PET/CT. The systematic review identified 11 publications describing either radiation treatment in FOP or radiation therapy as a cause of HO in non-FOP patients. Six case reports described the use of radiation in FOP patients for various reasons, including one with a high-dose treatment of a lip BCC using superficial X-ray therapy. The remaining five studies described the use of low-dose radiotherapy to prevent or treat either an FOP flare-up or HO formation. None of these cases showed worsening of disease that could be attributed to the use of radiation therapy. Radiation induced HO in non-FOP patients was rare and occurred in five studies. The largest of these studies suggested that HO was induced after treatment with high doses, resulting in more widespread evidence of tissue damage, potentially being the end result of this damage. In conclusion, available reports suggest no contraindication to radiotherapy in FOP patients; although the number of cases was small, systematic toxicity reports often were not available, and none of the reports described high-dose, high-energy radiation treatment at locations such as muscle and joint regions. Frontiers Media S.A. 2020-02-12 /pmc/articles/PMC7028822/ /pubmed/32117050 http://dx.doi.org/10.3389/fendo.2020.00006 Text en Copyright © 2020 Botman, Netelenbos, Rustemeyer, Schoonmade, Nieuwenhuijzen, Teunissen, Visser, Raijmakers, Lammertsma, Dahele and Eekhoff. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Botman, Esmée
Netelenbos, Jan Coen
Rustemeyer, Thomas
Schoonmade, Linda J.
Nieuwenhuijzen, Jakko A.
Teunissen, Bernd P.
Visser, Marieke
Raijmakers, Pieter
Lammertsma, Adriaan A.
Dahele, Max
Eekhoff, Marelise
Radiotherapy in Fibrodysplasia Ossificans Progressiva: A Case Report and Systematic Review of the Literature
title Radiotherapy in Fibrodysplasia Ossificans Progressiva: A Case Report and Systematic Review of the Literature
title_full Radiotherapy in Fibrodysplasia Ossificans Progressiva: A Case Report and Systematic Review of the Literature
title_fullStr Radiotherapy in Fibrodysplasia Ossificans Progressiva: A Case Report and Systematic Review of the Literature
title_full_unstemmed Radiotherapy in Fibrodysplasia Ossificans Progressiva: A Case Report and Systematic Review of the Literature
title_short Radiotherapy in Fibrodysplasia Ossificans Progressiva: A Case Report and Systematic Review of the Literature
title_sort radiotherapy in fibrodysplasia ossificans progressiva: a case report and systematic review of the literature
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028822/
https://www.ncbi.nlm.nih.gov/pubmed/32117050
http://dx.doi.org/10.3389/fendo.2020.00006
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