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Bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report
BACKGROUND: Bizarre parosteal osteochondromatous proliferation (BPOP) is a relatively rare benign extraperiosteal osteochondroma-like proliferative lesion that shares similarities with malignant tumours in terms of morphology. The aetiology of BPOP has yet to be determined and there are no previous...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069180/ https://www.ncbi.nlm.nih.gov/pubmed/32164617 http://dx.doi.org/10.1186/s12891-020-3168-x |
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author | Yao, Ruoyu Goh, En Lin Fan, Zhaoxiang Wu, Xuequn Feng, Yanqi |
author_facet | Yao, Ruoyu Goh, En Lin Fan, Zhaoxiang Wu, Xuequn Feng, Yanqi |
author_sort | Yao, Ruoyu |
collection | PubMed |
description | BACKGROUND: Bizarre parosteal osteochondromatous proliferation (BPOP) is a relatively rare benign extraperiosteal osteochondroma-like proliferative lesion that shares similarities with malignant tumours in terms of morphology. The aetiology of BPOP has yet to be determined and there are no previous reports of BPOP associated with fracture. CASE PRESENTATION: A 57-year-old woman presented with a one-month history of pain and swelling in her right foot, which were worsened by activity and improved with rest. Physical examination revealed a hard, non-mobile mass measuring 1.5 cm × 1.5 cm on the dorsal aspect of the third metatarsal of the right foot. There was overlying erythema and tenderness on palpation. Computed tomography (CT) of the right foot demonstrated a fracture of the neck of the third metatarsal, osteolysis at the fracture site and soft tissue swelling. Bone scintigraphy revealed increased tracer uptake suggesting abnormal bone metabolism at the neck of the third metatarsal. Surgical excision of the lesion was performed. Histopathology and immunohistochemistry confirmed the diagnosis of BPOP. CONCLUSION: BPOP is a rare benign lesion that is commonly misdiagnosed. Differential diagnosis is mainly achieved through imaging and histopathological assessment. |
format | Online Article Text |
id | pubmed-7069180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70691802020-03-18 Bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report Yao, Ruoyu Goh, En Lin Fan, Zhaoxiang Wu, Xuequn Feng, Yanqi BMC Musculoskelet Disord Case Report BACKGROUND: Bizarre parosteal osteochondromatous proliferation (BPOP) is a relatively rare benign extraperiosteal osteochondroma-like proliferative lesion that shares similarities with malignant tumours in terms of morphology. The aetiology of BPOP has yet to be determined and there are no previous reports of BPOP associated with fracture. CASE PRESENTATION: A 57-year-old woman presented with a one-month history of pain and swelling in her right foot, which were worsened by activity and improved with rest. Physical examination revealed a hard, non-mobile mass measuring 1.5 cm × 1.5 cm on the dorsal aspect of the third metatarsal of the right foot. There was overlying erythema and tenderness on palpation. Computed tomography (CT) of the right foot demonstrated a fracture of the neck of the third metatarsal, osteolysis at the fracture site and soft tissue swelling. Bone scintigraphy revealed increased tracer uptake suggesting abnormal bone metabolism at the neck of the third metatarsal. Surgical excision of the lesion was performed. Histopathology and immunohistochemistry confirmed the diagnosis of BPOP. CONCLUSION: BPOP is a rare benign lesion that is commonly misdiagnosed. Differential diagnosis is mainly achieved through imaging and histopathological assessment. BioMed Central 2020-03-12 /pmc/articles/PMC7069180/ /pubmed/32164617 http://dx.doi.org/10.1186/s12891-020-3168-x Text en © The Author(s). 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Case Report Yao, Ruoyu Goh, En Lin Fan, Zhaoxiang Wu, Xuequn Feng, Yanqi Bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report |
title | Bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report |
title_full | Bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report |
title_fullStr | Bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report |
title_full_unstemmed | Bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report |
title_short | Bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report |
title_sort | bizarre parosteal osteochondromatous proliferation co-occurring with a metatarsal fatigue fracture: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069180/ https://www.ncbi.nlm.nih.gov/pubmed/32164617 http://dx.doi.org/10.1186/s12891-020-3168-x |
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