Pediatric soft tissue tumors. Tumors of uncertain origin

被引：0
|
作者：
Greimelmaier, K. [1 ]
Vokuhl, C. [1 ]
机构：
[1] Univ Klinikum Bonn, Inst Pathol, Sekt Kinderpathol, Venusberg Campus 1, D-53127 Bonn, Germany
来源：
PATHOLOGIE | 2024年
关键词：
Angiomatoid fibrous histiocytoma; Alveolar soft part sarcoma; Synovial sarcoma; Rhabdoid tumor; Desmoplastic small round cell tumor; ROUND-CELL TUMOR; MALIGNANT FIBROUS HISTIOCYTOMA; SYNOVIAL SARCOMA; PART SARCOMA; GENE FUSIONS; EWSR1-CREB1; EXPRESSION; EMPHASIS; SPECTRUM; WT1;
D O I：
10.1007/s00292-024-01356-z
中图分类号：
R36 [病理学];
学科分类号：
100104 ;
摘要：
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.
引用
收藏
页码：412 / 421
页数：10
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