| Literature DB >> 28656498 |
L Max Almond1, Adrian T Warfield2, Anant Desai3, David Gourevitch3, Samuel J Ford3.
Abstract
Carcinosarcomas (CS) are uncommon, highly aggressive, biphasic tumours consisting of both sarcomatous and carcinomatous elements. They appear to originate from a common cell of origin, either via transformation from a single premature precursor or conversion of a mature epithelial cell through an epithelial-mesenchymal transition. CS should be considered a unique cancer subtype with cells typically displaying diffuse mitotic activity and widespread atypical mitoses predisposing to early metastasis and a tendency to local recurrence following resection. This review addresses the pathophysiology of CS and discusses its presentation, natural history and management at a variety of sites within the abdominal cavity and retroperitoneum.Entities:
Keywords: Biphasic tumour; Carcinosarcoma; Malignant mixed mullerian tumour; Sarcomatoid carcinoma
Mesh:
Year: 2017 PMID: 28656498 DOI: 10.1007/s10147-017-1153-7
Source DB: PubMed Journal: Int J Clin Oncol ISSN: 1341-9625 Impact factor: 3.402