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EWSR1::WT1 Fusions in Neoplasms Other Than Conventional Desmoplastic Small Round Cell Tumor: Three Tumors Occurring Outside the Female Genital Tract.
Warmke, Laura M; Perret, Raul; Ledoux, Pauline; Michot, Audrey; Italiano, Antoine; Zou, Ying S; Matoso, Andres; Argani, Pedram; Ulbright, Thomas M; Baumhoer, Daniel; Ameline, Baptiste; Gross, John M.
Afiliação
  • Warmke LM; Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana. Electronic address: lwarmke@iu.edu.
  • Perret R; Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France; Bordeaux Institute of Oncology, BRIC, INSERM, Bordeaux University, Bergonié Institute, Bordeaux, France.
  • Ledoux P; Department of Diagnostic and Interventional Oncological Imaging, Institut Bergonié, Regional Comprehensive Cancer of Nouvelle-Aquitaine, Bordeaux, France.
  • Michot A; Plastic and Reconstructive Surgery Department, Bergonié Institute, Bordeaux, France.
  • Italiano A; Sarcoma Unit, Institut Bergonié, Bordeaux, Gironde, France; Faculty of Medicine, University of Bordeaux, Bordeaux, Gironde, France.
  • Zou YS; Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland.
  • Matoso A; Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland.
  • Argani P; Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland.
  • Ulbright TM; Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana.
  • Baumhoer D; Bone Tumor Reference Center at the Institute of Pathology, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Ameline B; Bone Tumor Reference Center at the Institute of Pathology, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Gross JM; Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland.
Mod Pathol ; 37(3): 100418, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38158126
ABSTRACT
Desmoplastic small round cell tumor (DSRCT) is a high-grade, primitive round cell sarcoma classically associated with prominent desmoplastic stroma, coexpression of keratin and desmin, and a characteristic EWSR1WT1 gene fusion. DSRCT typically arises in the abdominopelvic cavity of young males with diffuse peritoneal spread and poor overall survival. Although originally considered to be pathognomonic for DSRCT, EWSR1WT1 gene fusions have recently been detected in rare tumors lacking the characteristic morphologic and immunohistochemical features of DSRCT. Here, we report 3 additional cases of neoplasms other than conventional DSCRCT with EWSR1WT1 gene fusions that occurred outside the female genital tract. Two occurred in the abdominopelvic cavities of a 27-year-old man and a 12-year-old girl, whereas the third arose in the axillary soft tissue of an 85-year-old man. All cases lacked prominent desmoplastic stroma and were instead solid and cystic with peripheral fibrous pseudocapsules and occasional intervening fibrous septa. Necrosis was either absent (1/3) or rare (2/3), and mitotic activity was low (<1 to 3 per 10 hpf). In immunohistochemical studies, there was expression of smooth muscle actin (3/3) and desmin (3/3), rare to focal reactivity for EMA (2/3), and variable expression of CK AE1/AE3 (1/3). Myogenin and MyoD1 were negative, and C-terminus-specific WT1 was positive in both cases tested (2/2). All 3 tumors followed a more indolent clinical course with 2 cases demonstrating no evidence of disease at 20 and 44 months after resection. The patient from case 3 died of other causes at 14 months with no evidence of recurrence. DNA methylation profiling showed that the 3 cases clustered with DSRCT; however, they demonstrated fewer copy number variations with 2 cases having a flat profile (0% copy number variation). Differential methylation analysis with hierarchical clustering further showed variation between the 3 cases and conventional DSRCT. Although further study is needed, our results, in addition to previous reports, suggest that EWSR1WT1 gene fusions occur in rare and seemingly distinctive tumors other than conventional DSRCT with indolent behavior. Proper classification of these unusual soft tissue tumors with EWSR1WT1 gene fusions requires direct correlation with tumor morphology and clinical behavior, which is essential to avoid overtreatment with aggressive chemotherapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias de Tecidos Moles / Tumor Desmoplásico de Pequenas Células Redondas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias de Tecidos Moles / Tumor Desmoplásico de Pequenas Células Redondas Idioma: En Ano de publicação: 2024 Tipo de documento: Article