NSTL国家科技图书文献中心

1. Paediatric renal tumours: an update on challenges and recent developments NSTL国家科技图书文献中心

Somers, Gino R. | L'Hermine-Coulomb, A...... - 《Virchows Archiv》 - 2025,486(1) - 49～64 - 共16页

摘要： the typically lethal malignant* rhabdoid tumour, form | . These include the embryonal tumour nephroblastoma* | Paediatric renal tumours include a broad range | of neoplasms which largely differ, but also overlap | to a smaller extent, with adult kidney cancer

关键词： Nephroblastoma | Paediatric renal tumour | Wilms' tumour | Clear cell sarcoma of kidney | Congenital mesoblastic nephroma | Malignant rhabdoid tumour | Renal cell carcinoma

2. Pediatric Atypical Teratoid Rhabdoid Tumor of Central Nervous System: A Case Series with Review of Literature NSTL国家科技图书文献中心

Verma, Jyoti | Gupta, Neelima ... - 《Indian journal of surgical oncology》 - 2025,16(2) - 611～620 - 共10页

摘要：Atypical teratoid rhabdoid* tumor (AT/RT) of* | , aggressive malignant* neoplasm of infancy and early* | the central nervous system (CNS) is the rare | childhood and relatively rare in adults. Patients with | ATRT typically follow a dismal course. Because of its

关键词： Atypical teratoid/rhabdoid tumor | Histopathological | Immunohistochemical

3. SMARCA4-deficient primary bone sarcoma with "teratoid" features in a rhabdoid tumor predisposition syndrome patient NSTL国家科技图书文献中心

Sookdeo, Jonathan | Wang, Lu ... - 《Virchows Archiv》 - 2025,486(3) - 611～616 - 共6页

摘要： to rhabdoid* tumor predisposition syndrome type 2* | hypercalcemic type (SCCOHT) and pediatric rhabdoid* tumors. To* | Abstract SMARCA4 is a catalytic subunit of the | SWItch/sucrose non-fermentable (SWI/SNF) complex | . Truncating SMARCA4 germline pathogenic variants (PVs) lead

关键词： SMARCA4 | BRG1 | Rhabdoid tumor predisposition syndrome | SWI/SNF complex | Teratocarcinosarcoma | Bone sarcoma

4. Rhabdoid Tumor of the Kidney and Soft Tissues: Results from National Wilms Tumor Study‐5 and Children's Oncology Group Study AREN0321 NSTL国家科技图书文献中心

James I. Geller | Lindsay A. Renfro ... - 《Pediatric blood & cancer.》 - 2025,72(3) - e31490～e31490 - 共11页

摘要： malignant rhabdoid tumor of soft tissues (MRT). Patients | children with rhabdoid* tumor of the kidney (RTK) and* | improvement, outcomes for patients with rhabdoid tumor | ABSTRACT Purpose National Wilms Tumor Study‐5 | (NWTS‐5) and AREN0321 evaluated the outcomes of

关键词： chemotherapy | pediatric oncology | renal | rhabdoid tumor | tumors

5. Crucial role of preserving umbilical cord stumps for genetic decoding of a family with rhabdoid tumor predisposition syndrome NSTL国家科技图书文献中心

Pradeepkumar, Muruga... | Kandhakumar, Vignesh ... - 《Gene》 - 2025,948 - Article 149353～Article 149353 - 共4页

摘要：Background: The Rhabdoid* tumor is an* | can result in Rhabdoid* tumor predisposition syndrome* | ; (p.Arg40Ter) in the SMARCB1 gene causing Rhabdoid tumor | aggressive tumor that is commonly found in infants and | children with a prevalence of about, 0.6 in every 1

关键词： Rhabdoid tumor predisposition syndrome | Recurrent child loss | Dried umbilical cord stumps | SMARCB1 gene | Whole exome sequencing

6. Development of a Nomogram and Risk Grouping System for Predicting 1-Year Overall Survival of Patients With Atypical Teratoid/Rhabdoid Tumors NSTL国家科技图书文献中心

Kang, Xu | Zhou, Yabing ... - 《Journal of child neurology》 - 2025,40(3) - 153～161 - 共9页

摘要：Purpose Atypical teratoid/rhabdoid* tumor (AT* | with atypical teratoid/rhabdoid* tumor. Methods The* | /rhabdoid* tumor were included from the database. Cox* | atypical teratoid/rhabdoid* tumor patients was generated* | survival for atypical teratoid/rhabdoid* tumor patients*

关键词： atypical teratoid/rhabdoid tumor | nomogram | prognosis | risk grouping system | treatment

7. " Update on pediatric primary liver tumors " NSTL国家科技图书文献中心

Lopez-Terrada, Dolor... | Stahlschmidt, Jens ... - 《Virchows Archiv》 - 2025,486(1) - 23～47 - 共25页

摘要： and malignant* rhabdoid tumor. Malignant vascular* | primary malignant* neoplasms are rare, representing only* | ). Malignant* mesenchymal neoplasms represent approximately 10* | patients with malignant* liver tumors has been* | International Tumour* Trial) and other therapeutic protocols*

关键词： Childhood | Liver | Tumor | Epithelial | Mesenchymal | Hepatoblastoma

8. Switch/Sucrose Nofermentable-Deficient Tumors-Morphology, Immunophenotype, Genetics, Epigenetics, Nosology, and Therapy NSTL国家科技图书文献中心

Ng, Chi Sing | Qin, Jilong - 《Laboratory investigation》 - 2025,105(1) - 102185～102185 - 共13页

摘要：; SMARCA4/A2-deficient), malignant* rhabdoid tumor, and | , often with a variable component of rhabdoid tumor* | prognosis. Rhabdoid* tumor cell phenotype is a useful* | About 20% of human cancers harbor mutations of | genes encoding switch/sucrose nonfermentable (SWI/SNF

关键词： dedifferentiation | epigenetics | genetics | rhabdoid cells | SWI/SNF deficiency | undifferentiation

9. Proximal and Classic Epithelioid Sarcomas are Distinct Molecular Entities Defined by MYC/GATA3 and SOX17/Endothelial Markers, Respectively NSTL国家科技图书文献中心

Sigalotti, Luca | Frezza, Anna Maria ... - 《Modern pathology》 - 2025,38(1) - 100647～100647 - 共14页

摘要： the "MYC subgroup" of atypical teratoid/ rhabdoid | tumor, another SMARCB1-deficient tumor, implying a | Epithelioid sarcoma (ES) is a rare tumor | hallmarked by the loss of INI1/SMARCB1 expression. Apart | from this alteration, little is known about the

关键词： diagnostic biomarkers epigenomics | epithelioid sarcoma | next-generation sequencing | soft-tissue sarcoma | transcriptional profiling

10. SMARCB1 -deficient malignant melanocytic uveal tumours: a new neural crest-derived tumour entity with SMARCB1 -related germline predisposition NSTL国家科技图书文献中心

Cyrta, Joanna | Masliah-Planchon, Ju...... - 《Journal of Pathology》 - 2025,265(3) - 357～371 - 共15页

摘要：Rhabdoid tumours (RT) are an aggressive | malignancy affecting <2-year-old infants, characterised by | biallelic loss-of-function alterations in SWI/SNF-related | BAF chromatin remodelling complex subunit B1 | (SMARCB1) in nearly all cases. Germline SMARCB1

摘要： the typically lethal malignant* rhabdoid tumour, form | . These include the embryonal tumour nephroblastoma* | Paediatric renal tumours include a broad range | of neoplasms which largely differ, but also overlap | to a smaller extent, with adult kidney cancer

关键词： Nephroblastoma | Paediatric renal tumour | Wilms' tumour | Clear cell sarcoma of kidney | Congenital mesoblastic nephroma | Malignant rhabdoid tumour | Renal cell carcinoma

摘要：Atypical teratoid rhabdoid* tumor (AT/RT) of* | , aggressive malignant* neoplasm of infancy and early* | the central nervous system (CNS) is the rare | childhood and relatively rare in adults. Patients with | ATRT typically follow a dismal course. Because of its

关键词： Atypical teratoid/rhabdoid tumor | Histopathological | Immunohistochemical

摘要： to rhabdoid* tumor predisposition syndrome type 2* | hypercalcemic type (SCCOHT) and pediatric rhabdoid* tumors. To* | Abstract SMARCA4 is a catalytic subunit of the | SWItch/sucrose non-fermentable (SWI/SNF) complex | . Truncating SMARCA4 germline pathogenic variants (PVs) lead

关键词： SMARCA4 | BRG1 | Rhabdoid tumor predisposition syndrome | SWI/SNF complex | Teratocarcinosarcoma | Bone sarcoma

摘要： malignant rhabdoid tumor of soft tissues (MRT). Patients | children with rhabdoid* tumor of the kidney (RTK) and* | improvement, outcomes for patients with rhabdoid tumor | ABSTRACT Purpose National Wilms Tumor Study‐5 | (NWTS‐5) and AREN0321 evaluated the outcomes of

关键词： chemotherapy | pediatric oncology | renal | rhabdoid tumor | tumors

摘要：Background: The Rhabdoid* tumor is an* | can result in Rhabdoid* tumor predisposition syndrome* | ; (p.Arg40Ter) in the SMARCB1 gene causing Rhabdoid tumor | aggressive tumor that is commonly found in infants and | children with a prevalence of about, 0.6 in every 1

关键词： Rhabdoid tumor predisposition syndrome | Recurrent child loss | Dried umbilical cord stumps | SMARCB1 gene | Whole exome sequencing

摘要：Purpose Atypical teratoid/rhabdoid* tumor (AT* | with atypical teratoid/rhabdoid* tumor. Methods The* | /rhabdoid* tumor were included from the database. Cox* | atypical teratoid/rhabdoid* tumor patients was generated* | survival for atypical teratoid/rhabdoid* tumor patients*

关键词： atypical teratoid/rhabdoid tumor | nomogram | prognosis | risk grouping system | treatment

摘要： and malignant* rhabdoid tumor. Malignant vascular* | primary malignant* neoplasms are rare, representing only* | ). Malignant* mesenchymal neoplasms represent approximately 10* | patients with malignant* liver tumors has been* | International Tumour* Trial) and other therapeutic protocols*

关键词： Childhood | Liver | Tumor | Epithelial | Mesenchymal | Hepatoblastoma

摘要：; SMARCA4/A2-deficient), malignant* rhabdoid tumor, and | , often with a variable component of rhabdoid tumor* | prognosis. Rhabdoid* tumor cell phenotype is a useful* | About 20% of human cancers harbor mutations of | genes encoding switch/sucrose nonfermentable (SWI/SNF

关键词： dedifferentiation | epigenetics | genetics | rhabdoid cells | SWI/SNF deficiency | undifferentiation

摘要： the "MYC subgroup" of atypical teratoid/ rhabdoid | tumor, another SMARCB1-deficient tumor, implying a | Epithelioid sarcoma (ES) is a rare tumor | hallmarked by the loss of INI1/SMARCB1 expression. Apart | from this alteration, little is known about the

关键词： diagnostic biomarkers epigenomics | epithelioid sarcoma | next-generation sequencing | soft-tissue sarcoma | transcriptional profiling

摘要：Rhabdoid tumours (RT) are an aggressive | malignancy affecting <2-year-old infants, characterised by | biallelic loss-of-function alterations in SWI/SNF-related | BAF chromatin remodelling complex subunit B1 | (SMARCB1) in nearly all cases. Germline SMARCB1

关键词： SMARCB1 | uveal melanoma | rhabdoid tumour | RTPS1 | SWI/SNF | BAF47 | INI1 | genomics | neural crest | eye cancer

4008-161-200 800-990-8900

国家科技图书文献中心

摘要： the typically lethal malignant rhabdoid tumour, form | . These include the embryonal tumour nephroblastoma | Paediatric renal tumours include a broad range | of neoplasms which largely differ, but also overlap | to a smaller extent, with adult kidney cancer

关键词： Nephroblastoma | Paediatric renal tumour | Wilms' tumour | Clear cell sarcoma of kidney | Congenital mesoblastic nephroma | Malignant rhabdoid tumour | Renal cell carcinoma

摘要：Atypical teratoid rhabdoid tumor (AT/RT) of | , aggressive malignant neoplasm of infancy and early | the central nervous system (CNS) is the rare | childhood and relatively rare in adults. Patients with | ATRT typically follow a dismal course. Because of its

关键词： Atypical teratoid/rhabdoid tumor | Histopathological | Immunohistochemical

摘要： to rhabdoid tumor predisposition syndrome type 2 | hypercalcemic type (SCCOHT) and pediatric rhabdoid tumors. To | Abstract SMARCA4 is a catalytic subunit of the | SWItch/sucrose non-fermentable (SWI/SNF) complex | . Truncating SMARCA4 germline pathogenic variants (PVs) lead

关键词： SMARCA4 | BRG1 | Rhabdoid tumor predisposition syndrome | SWI/SNF complex | Teratocarcinosarcoma | Bone sarcoma

摘要： malignant rhabdoid tumor of soft tissues (MRT). Patients | children with rhabdoid tumor of the kidney (RTK) and | improvement, outcomes for patients with rhabdoid tumor | ABSTRACT Purpose National Wilms Tumor Study‐5 | (NWTS‐5) and AREN0321 evaluated the outcomes of

关键词： chemotherapy | pediatric oncology | renal | rhabdoid tumor | tumors

摘要：Background: The Rhabdoid tumor is an | can result in Rhabdoid tumor predisposition syndrome | ; (p.Arg40Ter) in the SMARCB1 gene causing Rhabdoid tumor | aggressive tumor that is commonly found in infants and | children with a prevalence of about, 0.6 in every 1

关键词： Rhabdoid tumor predisposition syndrome | Recurrent child loss | Dried umbilical cord stumps | SMARCB1 gene | Whole exome sequencing

摘要：Purpose Atypical teratoid/rhabdoid tumor (AT | with atypical teratoid/rhabdoid tumor. Methods The | /rhabdoid tumor were included from the database. Cox | atypical teratoid/rhabdoid tumor patients was generated | survival for atypical teratoid/rhabdoid tumor patients

关键词： atypical teratoid/rhabdoid tumor | nomogram | prognosis | risk grouping system | treatment

摘要： and malignant rhabdoid tumor. Malignant vascular | primary malignant neoplasms are rare, representing only | ). Malignant mesenchymal neoplasms represent approximately 10 | patients with malignant liver tumors has been | International Tumour Trial) and other therapeutic protocols

关键词： Childhood | Liver | Tumor | Epithelial | Mesenchymal | Hepatoblastoma

摘要：; SMARCA4/A2-deficient), malignant rhabdoid tumor, and | , often with a variable component of rhabdoid tumor | prognosis. Rhabdoid tumor cell phenotype is a useful | About 20% of human cancers harbor mutations of | genes encoding switch/sucrose nonfermentable (SWI/SNF

关键词： dedifferentiation | epigenetics | genetics | rhabdoid cells | SWI/SNF deficiency | undifferentiation

摘要： the "MYC subgroup" of atypical teratoid/ rhabdoid | tumor, another SMARCB1-deficient tumor, implying a | Epithelioid sarcoma (ES) is a rare tumor | hallmarked by the loss of INI1/SMARCB1 expression. Apart | from this alteration, little is known about the

关键词： diagnostic biomarkers epigenomics | epithelioid sarcoma | next-generation sequencing | soft-tissue sarcoma | transcriptional profiling

摘要：Rhabdoid tumours (RT) are an aggressive | malignancy affecting <2-year-old infants, characterised by | biallelic loss-of-function alterations in SWI/SNF-related | BAF chromatin remodelling complex subunit B1 | (SMARCB1) in nearly all cases. Germline SMARCB1

关键词： SMARCB1 | uveal melanoma | rhabdoid tumour | RTPS1 | SWI/SNF | BAF47 | INI1 | genomics | neural crest | eye cancer

4008-161-200 800-990-8900

国家科技图书文献中心

摘要： the typically lethal malignant* rhabdoid tumour, form | . These include the embryonal tumour nephroblastoma* | Paediatric renal tumours include a broad range | of neoplasms which largely differ, but also overlap | to a smaller extent, with adult kidney cancer

摘要：Atypical teratoid rhabdoid* tumor (AT/RT) of* | , aggressive malignant* neoplasm of infancy and early* | the central nervous system (CNS) is the rare | childhood and relatively rare in adults. Patients with | ATRT typically follow a dismal course. Because of its

摘要： to rhabdoid* tumor predisposition syndrome type 2* | hypercalcemic type (SCCOHT) and pediatric rhabdoid* tumors. To* | Abstract SMARCA4 is a catalytic subunit of the | SWItch/sucrose non-fermentable (SWI/SNF) complex | . Truncating SMARCA4 germline pathogenic variants (PVs) lead

摘要： malignant rhabdoid tumor of soft tissues (MRT). Patients | children with rhabdoid* tumor of the kidney (RTK) and* | improvement, outcomes for patients with rhabdoid tumor | ABSTRACT Purpose National Wilms Tumor Study‐5 | (NWTS‐5) and AREN0321 evaluated the outcomes of

摘要：Background: The Rhabdoid* tumor is an* | can result in Rhabdoid* tumor predisposition syndrome* | ; (p.Arg40Ter) in the SMARCB1 gene causing Rhabdoid tumor | aggressive tumor that is commonly found in infants and | children with a prevalence of about, 0.6 in every 1

摘要：Purpose Atypical teratoid/rhabdoid* tumor (AT* | with atypical teratoid/rhabdoid* tumor. Methods The* | /rhabdoid* tumor were included from the database. Cox* | atypical teratoid/rhabdoid* tumor patients was generated* | survival for atypical teratoid/rhabdoid* tumor patients*

摘要：; SMARCA4/A2-deficient), malignant* rhabdoid tumor, and | , often with a variable component of rhabdoid tumor* | prognosis. Rhabdoid* tumor cell phenotype is a useful* | About 20% of human cancers harbor mutations of | genes encoding switch/sucrose nonfermentable (SWI/SNF