Sacral chondroblastoma - a rare location, a rare pathology: A case report and review of literature.
Case report
Chondroblastoma
Immunohistochemistry
Pathology
Sacrum
Spine
Journal
World journal of clinical cases
ISSN: 2307-8960
Titre abrégé: World J Clin Cases
Pays: United States
ID NLM: 101618806
Informations de publication
Date de publication:
16 Jul 2021
16 Jul 2021
Historique:
received:
08
03
2021
revised:
28
03
2021
accepted:
20
05
2021
entrez:
26
7
2021
pubmed:
27
7
2021
medline:
27
7
2021
Statut:
ppublish
Résumé
Chondroblastoma (CB) is an intermediate tumor of cartilage origin. CB involving the sacrum is a very rare pathology. A 17-year-old male with sacral CB was diagnosed as CB during the first surgery, and 18 mo later, the tumor recurred and a second surgery was performed with the same pathology result of CB. We recommend complete removal of the tumor in a timely manner, provided that surgical conditions are met. At the same time, other diseases should be carefully differentiated in terms of imaging or pathological features so as to avoid erroneous diagnostic conclusions.
Sections du résumé
BACKGROUND
BACKGROUND
Chondroblastoma (CB) is an intermediate tumor of cartilage origin. CB involving the sacrum is a very rare pathology.
CASE SUMMARY
METHODS
A 17-year-old male with sacral CB was diagnosed as CB during the first surgery, and 18 mo later, the tumor recurred and a second surgery was performed with the same pathology result of CB.
CONCLUSION
CONCLUSIONS
We recommend complete removal of the tumor in a timely manner, provided that surgical conditions are met. At the same time, other diseases should be carefully differentiated in terms of imaging or pathological features so as to avoid erroneous diagnostic conclusions.
Identifiants
pubmed: 34307629
doi: 10.12998/wjcc.v9.i20.5709
pmc: PMC8281409
doi:
Types de publication
Case Reports
Langues
eng
Pagination
5709-5716Informations de copyright
©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.
Déclaration de conflit d'intérêts
Conflict-of-interest statement: The authors declare that they have no conflict-of-interest.
Références
Pathol Int. 2017 Oct;67(10):495-502
pubmed: 28971570
J Neurooncol. 2018 Oct;140(1):99-106
pubmed: 29968040
Am J Otolaryngol. 2020 Jul - Aug;41(4):102486
pubmed: 32305254
Br J Cancer. 1993 Dec;68(6):1134-9
pubmed: 8260365
Diagn Cytopathol. 1997 Jan;16(1):65-71
pubmed: 9034741
JBJS Case Connect. 2019 Jul-Sep;9(3):e0086
pubmed: 31469667
Clin Orthop Relat Res. 2005 Sep;438:103-9
pubmed: 16131877
J Neurosurg. 2018 Oct 12;131(3):695-705
pubmed: 30497189
Hum Pathol. 1995 Jun;26(6):620-4
pubmed: 7774891
Skeletal Radiol. 1999 Nov;28(11):644-50
pubmed: 10591928
Z Orthop Ihre Grenzgeb. 1967 Apr;102(4):625-9
pubmed: 4233032
Skeletal Radiol. 2017 Mar;46(3):367-372
pubmed: 27966029
Eur J Orthop Surg Traumatol. 2017 Aug;27(6):843-849
pubmed: 28634924
Skeletal Radiol. 2003 Feb;32(2):66-71
pubmed: 12589483
J Bone Joint Surg Br. 2005 Jul;87(7):974-8
pubmed: 15972914
Diagn Cytopathol. 1991;7(3):261-6
pubmed: 1879261
J Pediatr Orthop. 2019 Apr;39(4):e312-e317
pubmed: 30839485
Oncotarget. 2018 Jul 10;9(53):30106-30114
pubmed: 30046391
J Neurosurg Spine. 2005 May;2(5):596-600
pubmed: 15945435
Cancer Res Treat. 2009 Dec;41(4):241-4
pubmed: 20057972
Diagn Cytopathol. 2018 Jan;46(1):79-82
pubmed: 28834661
Diagn Cytopathol. 2007 Mar;35(3):154-7
pubmed: 17415918
Pediatr Radiol. 1987;17(5):392-6
pubmed: 3627860
World J Surg Oncol. 2020 Mar 2;18(1):47
pubmed: 32122388
Radiology. 1994 Feb;190(2):467-74
pubmed: 8284401
Diagn Cytopathol. 1985 Apr-Jun;1(2):111-7
pubmed: 3836075
Cancer. 1990 Apr 15;65(8):1847-63
pubmed: 2317764
Breast Cancer Res Treat. 2017 Nov;166(2):435-445
pubmed: 28795248