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Successful treatment with denosumab for pelvic fibrous dysplasia: A case report and review of the literature
RATIONALE: Fibrous dysplasia is a rare disorder that results in fractures, pain, and disability and can affect any bone in the body. The treatment of symptomatic fibrous dysplasia is determined based on the affected bones. Although some lesions are often too extensive for surgical procedures, there...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8663861/ https://www.ncbi.nlm.nih.gov/pubmed/34889277 http://dx.doi.org/10.1097/MD.0000000000028138 |
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author | Ikuta, Kunihiro Sakai, Tomohisa Koike, Hiroshi Ito, Kan Imagama, Shiro Nishida, Yoshihiro |
author_facet | Ikuta, Kunihiro Sakai, Tomohisa Koike, Hiroshi Ito, Kan Imagama, Shiro Nishida, Yoshihiro |
author_sort | Ikuta, Kunihiro |
collection | PubMed |
description | RATIONALE: Fibrous dysplasia is a rare disorder that results in fractures, pain, and disability and can affect any bone in the body. The treatment of symptomatic fibrous dysplasia is determined based on the affected bones. Although some lesions are often too extensive for surgical procedures, there are currently no effective or recommended medical treatments available for them. PATIENT CONCERNS: A 27-year-old woman developed right buttock pain and was diagnosed with a bone tumor in the right ilium. Clinical images revealed an expansive osteolytic lesion with thinning of the cortex and cystic change from the acetabulum to the sacroiliac joint. DIAGNOSIS: An incisional biopsy was performed, and the lesion was diagnosed as cystic fibrous dysplasia. Occasional osteoclast-like giant cells and woven bone were observed. The patient had no evidence of polyostotic lesions or findings of McCune-Albright syndrome. Biochemical blood test results showed no obvious abnormal values, except for an increase in serum tartrate-resistant acid phosphatase 5b to 459 mU/dL. INTERVENTIONS: Since surgical treatment appeared to be challenging, she was treated with denosumab with decreased dose-intensity schedules. OUTCOMES: The administration of denosumab caused osteosclerosis within the lesion, resulting in the elimination of bone pain. The patient received denosumab treatment for 18 months. Pain relief and lesion radiodensity were maintained for 9 months after denosumab discontinuation. The serum level of tartrate-resistant acid phosphatase 5b was measured to monitor the response to denosumab, which was suppressed during denosumab treatment. LESSONS: We described successful denosumab treatment in a patient with cystic fibrous dysplasia (FD) who maintained efficacy for 9 months after treatment. Although the use of denosumab in fibrous dysplasia is currently off-label, our experience with this patient supports the potential of denosumab therapy for patients for whom surgical treatment is challenging. |
format | Online Article Text |
id | pubmed-8663861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-86638612021-12-13 Successful treatment with denosumab for pelvic fibrous dysplasia: A case report and review of the literature Ikuta, Kunihiro Sakai, Tomohisa Koike, Hiroshi Ito, Kan Imagama, Shiro Nishida, Yoshihiro Medicine (Baltimore) 6900 RATIONALE: Fibrous dysplasia is a rare disorder that results in fractures, pain, and disability and can affect any bone in the body. The treatment of symptomatic fibrous dysplasia is determined based on the affected bones. Although some lesions are often too extensive for surgical procedures, there are currently no effective or recommended medical treatments available for them. PATIENT CONCERNS: A 27-year-old woman developed right buttock pain and was diagnosed with a bone tumor in the right ilium. Clinical images revealed an expansive osteolytic lesion with thinning of the cortex and cystic change from the acetabulum to the sacroiliac joint. DIAGNOSIS: An incisional biopsy was performed, and the lesion was diagnosed as cystic fibrous dysplasia. Occasional osteoclast-like giant cells and woven bone were observed. The patient had no evidence of polyostotic lesions or findings of McCune-Albright syndrome. Biochemical blood test results showed no obvious abnormal values, except for an increase in serum tartrate-resistant acid phosphatase 5b to 459 mU/dL. INTERVENTIONS: Since surgical treatment appeared to be challenging, she was treated with denosumab with decreased dose-intensity schedules. OUTCOMES: The administration of denosumab caused osteosclerosis within the lesion, resulting in the elimination of bone pain. The patient received denosumab treatment for 18 months. Pain relief and lesion radiodensity were maintained for 9 months after denosumab discontinuation. The serum level of tartrate-resistant acid phosphatase 5b was measured to monitor the response to denosumab, which was suppressed during denosumab treatment. LESSONS: We described successful denosumab treatment in a patient with cystic fibrous dysplasia (FD) who maintained efficacy for 9 months after treatment. Although the use of denosumab in fibrous dysplasia is currently off-label, our experience with this patient supports the potential of denosumab therapy for patients for whom surgical treatment is challenging. Lippincott Williams & Wilkins 2021-12-10 /pmc/articles/PMC8663861/ /pubmed/34889277 http://dx.doi.org/10.1097/MD.0000000000028138 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | 6900 Ikuta, Kunihiro Sakai, Tomohisa Koike, Hiroshi Ito, Kan Imagama, Shiro Nishida, Yoshihiro Successful treatment with denosumab for pelvic fibrous dysplasia: A case report and review of the literature |
title | Successful treatment with denosumab for pelvic fibrous dysplasia: A case report and review of the literature |
title_full | Successful treatment with denosumab for pelvic fibrous dysplasia: A case report and review of the literature |
title_fullStr | Successful treatment with denosumab for pelvic fibrous dysplasia: A case report and review of the literature |
title_full_unstemmed | Successful treatment with denosumab for pelvic fibrous dysplasia: A case report and review of the literature |
title_short | Successful treatment with denosumab for pelvic fibrous dysplasia: A case report and review of the literature |
title_sort | successful treatment with denosumab for pelvic fibrous dysplasia: a case report and review of the literature |
topic | 6900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8663861/ https://www.ncbi.nlm.nih.gov/pubmed/34889277 http://dx.doi.org/10.1097/MD.0000000000028138 |
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