Soft tissue tumors of childhood are an extremely heterogeneous group of tumors that require precise diagnosis for therapy. In this article, selected tumors of uncertain origin that exhibit characteristic histological, immunophenotypical, and molecular features are addressed. Angiomatoid fibrous histiocytoma, alveolar soft part sarcoma, extrarenal rhabdoid tumor, synovial sarcoma, and desmoplastic small round cell tumor differ in their pathology, their clinical behavior, and prognosis.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1007/s00292-024-01356-z | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!