Primary soft tissue sarcoma breast with multiphenotypic differentiation.

Breast cancer Cancer - see Oncology Chemotherapy Pathology

Journal

BMJ case reports
ISSN: 1757-790X
Titre abrégé: BMJ Case Rep
Pays: England
ID NLM: 101526291

Informations de publication

Date de publication:
22 Feb 2024
Historique:
medline: 23 2 2024
pubmed: 23 2 2024
entrez: 22 2 2024
Statut: epublish

Résumé

Primary soft tissue sarcomas of the breast are rare aggressive neoplasms. These often are misdiagnosed with other more common neoplasms like fibroepithelial malignancies, namely phyllodes tumour and metaplastic carcinoma. Being uncommon, chances of being misdiagnosed are higher leading to early mortality. A multidisciplinary team incorporating surgery, pathology, chemotherapy and radiotherapy is required to formulate an approach to primary soft tissue sarcoma. Generally, these tumours may show single or dual phenotype; we present one rare case report showing multiphenotypic differentiation.

Identifiants

pubmed: 38388202
pii: 17/2/e255750
doi: 10.1136/bcr-2023-255750
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Rashim Sharma (R)

Pathology and Lab Medicine, All India Institute of Medical Sciences Jodhpur, Jodhpur, Rajasthan, India.

Sudeep Khera (S)

Pathology and Lab Medicine, All India Institute of Medical Sciences Jodhpur, Jodhpur, Rajasthan, India drsudeepkhera@gmail.com.

Bharti Devnani (B)

Radiotherapy, All India Institute of Medical Sciences Jodhpur, Jodhpur, Rajasthan, India.

Sureka Binit (S)

Diagnostic and Interventional Radiology, All India Institute of Medical Sciences Jodhpur, Jodhpur, Rajasthan, India.

Classifications MeSH