(redirected from Rhabdoid Tumor)
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References in periodicals archive ?
In our case, we used the EpSSG pediatric rhabdoid tumor treatment protocol because the initial institutional diagnosis was a renal rhabdoid tumor.
Molecularly confirmed primary malignant rhabdoid tumor of the urinary bladder: Implications of accurate diagnosis.
Rhabdoid tumor is an extremely rare disease affecting kids.
Ten patients (29%) had a known history of systemic or malignant lesions at the time of biopsy, including 3 patients (9%) with Langerhans cell histiocytosis, 3 patients (9%) with osteosarcoma, 1 patient (3%) with Ewing sarcoma, 1 patient (3%) with rhabdoid tumor, 1 patient with malignant peripheral neural sheath tumor (MPNST) (3%), and 1 patient (3%) with chondrosarcoma.
Other neoplasms which occur in this age group include mesoblastic nephroma, multi cystic nephroma, rhabdoid tumor, clear cell sarcoma, Ewing's sarcoma, PNET, desmoplastic small round cell tumor, meta nephric stromal tumor, poly phenotypic anaplastic sarcoma, ossifying renal tumor of infancy, embryonal sarcoma, intra renal teratoma, epitheloid tumor, intra renal pure yolk sac tumor.
These tumors are often a component of the rhabdoid tumor predisposition syndrome, characterized by germline mutations of SMARCB1/INI1 and manifested by a marked predisposition to the development of malignant rhabdoid tumors of infancy and early childhood.
Malignant extrarenal rhabdoid tumor most frequently arises in children younger than 3 years (78,79) and is composed of sheets of large polygonal cells.
Abnormalities in INI1 were first described in malignant rhabdoid tumors (renal, extrarenal, and atypical teratoid/ rhabdoid tumor of the central nervous system), and loss of INI1 expression is seen in nearly all of these tumors.
Tumors That Frequently or Rarely Coexpress Cytokeratin and Vimentin Carcinomas that frequently express both Anaplastic thyroid carcinoma Endometrial carcinoma Mesothelioma Metaplastic breast carcinoma Myoepithelial carcinoma Renal cell carcinoma Sarcomatoid carcinoma Thyroid carcinomas Mesenchymal tumors that frequently express both Adamantinoma Chordoma DPSRCT Epithelioid angiosarcoma Epithelioid sarcoma Leiomyosarcoma Malignant rhabdoid tumor Synovial sarcoma Carcinomas that rarely express both Breast carcinoma GI carcinoma Lung, non-small cell carcinoma Ovarian carcinoma Prostatic carcinoma Small cell carcinoma Abbreviations: DPSRCT, desmoplastic small round cell tumor; GI, gastrointestinal.
In pediatric pathology a distinct neoplasm termed rhabdoid tumor of the kidney is recognized as a high-grade malignancy composed entirely of rhabdoid cells without true skeletal muscle differentiation.
For instance, rhabdoid tumor of the kidney is composed of dyscohesive round or polygonal cells having a round or indented nucleus with a central eosinophilic nucleolus.
Prognostic significance of dysadherin expression in epithelioid sarcoma and its diagnostic utility in distinguishing epithelioid sarcoma from malignant rhabdoid tumor.