Cargando…

Osteoid osteoma of the rib: A report of an extremely rare condition

INTRODUCTION: Osteoid osteoma (OO) is a type of benign bone tumor that usually affects long bones of the lower extremities. In this case report, we describe a successful surgical resection of an OO located in the rib which is an extremely rare location. CASE PRESENTATION: This is a 23-year-old man,...

Descripción completa

Detalles Bibliográficos
Autores principales: El Haj, Najat Id, Hafidi, Sara, Karam, Rajaa, Boubia, Souheil, Karkouri, Mehdi, Ridai, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097650/
https://www.ncbi.nlm.nih.gov/pubmed/35658306
http://dx.doi.org/10.1016/j.ijscr.2022.107139
_version_ 1784706221199065088
author El Haj, Najat Id
Hafidi, Sara
Karam, Rajaa
Boubia, Souheil
Karkouri, Mehdi
Ridai, Mohamed
author_facet El Haj, Najat Id
Hafidi, Sara
Karam, Rajaa
Boubia, Souheil
Karkouri, Mehdi
Ridai, Mohamed
author_sort El Haj, Najat Id
collection PubMed
description INTRODUCTION: Osteoid osteoma (OO) is a type of benign bone tumor that usually affects long bones of the lower extremities. In this case report, we describe a successful surgical resection of an OO located in the rib which is an extremely rare location. CASE PRESENTATION: This is a 23-year-old man, referred to our thoracic surgery department for a very intense nocturnal right chest pain for over two months, the physical examination was normal without clinically palpable chest mass. The CT scan showed an osteocondensing lesion at the junction of the middle and posterior arches of the right 6th rib suggesting Ewing's sarcoma, a PET CT was then requested showed an appearance of a regular non-hypermetabolic inhomogeneous condensation at the junction of the middle and posterior arcs of the 6th right rib. After multidisciplinary concertation, a CT-guided biopsy of the lesion was performed, the histological examination of which revealed an osteoid osteoma, then a complete resection of the lesion was performed under posterolateral thoracotomy which histology confirmed a costal osteoid osteoma. The patient is currently in good health condition with complete disappearance of chest pain after one month of the operation and does not present any complications for the long-term follow-up. DISCUSSION: Osteoid osteoma (OO) is a benign primary bone tumor with unknown pathogenesis. That occurs in patients during the first two decades of life in about 60 to 75% of cases with a strong predilection for long bones, in 60 to 70% of cases. Flat bones, such as the skull, jawbones, innominate bones, and ribs are rarely described (McDermott et al., 1996 [1]). The standard treatment for OO is complete surgical excision, which is offered to the patient when the pain is chronic and not relieved by medical treatment (Osteoid osteoma: the results of surgical treatment [Internet] [2]). CONCLUSION: The osteoid osteoma of the rib is a very rare entity of bone neoplasms, this is the first case in our department that demonstrates that the OO of the rib must be suspected affront any painful rib and that complete surgical excision when it's possible, is a safe and effective treatment.
format Online
Article
Text
id pubmed-9097650
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-90976502022-05-13 Osteoid osteoma of the rib: A report of an extremely rare condition El Haj, Najat Id Hafidi, Sara Karam, Rajaa Boubia, Souheil Karkouri, Mehdi Ridai, Mohamed Int J Surg Case Rep Case Report INTRODUCTION: Osteoid osteoma (OO) is a type of benign bone tumor that usually affects long bones of the lower extremities. In this case report, we describe a successful surgical resection of an OO located in the rib which is an extremely rare location. CASE PRESENTATION: This is a 23-year-old man, referred to our thoracic surgery department for a very intense nocturnal right chest pain for over two months, the physical examination was normal without clinically palpable chest mass. The CT scan showed an osteocondensing lesion at the junction of the middle and posterior arches of the right 6th rib suggesting Ewing's sarcoma, a PET CT was then requested showed an appearance of a regular non-hypermetabolic inhomogeneous condensation at the junction of the middle and posterior arcs of the 6th right rib. After multidisciplinary concertation, a CT-guided biopsy of the lesion was performed, the histological examination of which revealed an osteoid osteoma, then a complete resection of the lesion was performed under posterolateral thoracotomy which histology confirmed a costal osteoid osteoma. The patient is currently in good health condition with complete disappearance of chest pain after one month of the operation and does not present any complications for the long-term follow-up. DISCUSSION: Osteoid osteoma (OO) is a benign primary bone tumor with unknown pathogenesis. That occurs in patients during the first two decades of life in about 60 to 75% of cases with a strong predilection for long bones, in 60 to 70% of cases. Flat bones, such as the skull, jawbones, innominate bones, and ribs are rarely described (McDermott et al., 1996 [1]). The standard treatment for OO is complete surgical excision, which is offered to the patient when the pain is chronic and not relieved by medical treatment (Osteoid osteoma: the results of surgical treatment [Internet] [2]). CONCLUSION: The osteoid osteoma of the rib is a very rare entity of bone neoplasms, this is the first case in our department that demonstrates that the OO of the rib must be suspected affront any painful rib and that complete surgical excision when it's possible, is a safe and effective treatment. Elsevier 2022-05-06 /pmc/articles/PMC9097650/ /pubmed/35658306 http://dx.doi.org/10.1016/j.ijscr.2022.107139 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
El Haj, Najat Id
Hafidi, Sara
Karam, Rajaa
Boubia, Souheil
Karkouri, Mehdi
Ridai, Mohamed
Osteoid osteoma of the rib: A report of an extremely rare condition
title Osteoid osteoma of the rib: A report of an extremely rare condition
title_full Osteoid osteoma of the rib: A report of an extremely rare condition
title_fullStr Osteoid osteoma of the rib: A report of an extremely rare condition
title_full_unstemmed Osteoid osteoma of the rib: A report of an extremely rare condition
title_short Osteoid osteoma of the rib: A report of an extremely rare condition
title_sort osteoid osteoma of the rib: a report of an extremely rare condition
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097650/
https://www.ncbi.nlm.nih.gov/pubmed/35658306
http://dx.doi.org/10.1016/j.ijscr.2022.107139
work_keys_str_mv AT elhajnajatid osteoidosteomaoftheribareportofanextremelyrarecondition
AT hafidisara osteoidosteomaoftheribareportofanextremelyrarecondition
AT karamrajaa osteoidosteomaoftheribareportofanextremelyrarecondition
AT boubiasouheil osteoidosteomaoftheribareportofanextremelyrarecondition
AT karkourimehdi osteoidosteomaoftheribareportofanextremelyrarecondition
AT ridaimohamed osteoidosteomaoftheribareportofanextremelyrarecondition