Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature
Abstract We describe the case of a 4-year-old boy with a unilateral right-sided Wilms tumor with stromal predominance and teratoid features, which was localized to the kidney and hence, was completely resected. The pediatric surgeon and pathologist, both should be aware of this rare appearance of ne...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Gupta, Ruchika [verfasserIn] Sharma, Alok [verfasserIn] Arora, Raman [verfasserIn] Dinda, Amit Kumar [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2009 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Pediatric surgery international - Berlin : Springer, 1986, 25(2009), 3 vom: 29. Jan., Seite 293-295 |
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| Übergeordnetes Werk: |
volume:25 ; year:2009 ; number:3 ; day:29 ; month:01 ; pages:293-295 |
| Links: |
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| DOI / URN: |
10.1007/s00383-009-2333-y |
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| Katalog-ID: |
SPR004710347 |
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| 245 | 1 | 0 | |a Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature |
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| 520 | |a Abstract We describe the case of a 4-year-old boy with a unilateral right-sided Wilms tumor with stromal predominance and teratoid features, which was localized to the kidney and hence, was completely resected. The pediatric surgeon and pathologist, both should be aware of this rare appearance of nephroblastoma so as to avoid the highly toxic chemotherapy and radiotherapy in such patients. | ||
| 650 | 4 | |a Nephroblastoma |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Teratoid |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Unilateral |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Histopathology |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Sharma, Alok |e verfasserin |4 aut | |
| 700 | 1 | |a Arora, Raman |e verfasserin |4 aut | |
| 700 | 1 | |a Dinda, Amit Kumar |e verfasserin |4 aut | |
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| allfields |
10.1007/s00383-009-2333-y doi (DE-627)SPR004710347 (SPR)s00383-009-2333-y-e DE-627 ger DE-627 rakwb eng 610 ASE 44.65 bkl 44.67 bkl Gupta, Ruchika verfasserin aut Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We describe the case of a 4-year-old boy with a unilateral right-sided Wilms tumor with stromal predominance and teratoid features, which was localized to the kidney and hence, was completely resected. The pediatric surgeon and pathologist, both should be aware of this rare appearance of nephroblastoma so as to avoid the highly toxic chemotherapy and radiotherapy in such patients. Nephroblastoma (dpeaa)DE-He213 Teratoid (dpeaa)DE-He213 Unilateral (dpeaa)DE-He213 Histopathology (dpeaa)DE-He213 Sharma, Alok verfasserin aut Arora, Raman verfasserin aut Dinda, Amit Kumar verfasserin aut Enthalten in Pediatric surgery international Berlin : Springer, 1986 25(2009), 3 vom: 29. Jan., Seite 293-295 (DE-627)254638937 (DE-600)1463010-2 1437-9813 nnns volume:25 year:2009 number:3 day:29 month:01 pages:293-295 https://dx.doi.org/10.1007/s00383-009-2333-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.65 ASE 44.67 ASE AR 25 2009 3 29 01 293-295 |
| spelling |
10.1007/s00383-009-2333-y doi (DE-627)SPR004710347 (SPR)s00383-009-2333-y-e DE-627 ger DE-627 rakwb eng 610 ASE 44.65 bkl 44.67 bkl Gupta, Ruchika verfasserin aut Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We describe the case of a 4-year-old boy with a unilateral right-sided Wilms tumor with stromal predominance and teratoid features, which was localized to the kidney and hence, was completely resected. The pediatric surgeon and pathologist, both should be aware of this rare appearance of nephroblastoma so as to avoid the highly toxic chemotherapy and radiotherapy in such patients. Nephroblastoma (dpeaa)DE-He213 Teratoid (dpeaa)DE-He213 Unilateral (dpeaa)DE-He213 Histopathology (dpeaa)DE-He213 Sharma, Alok verfasserin aut Arora, Raman verfasserin aut Dinda, Amit Kumar verfasserin aut Enthalten in Pediatric surgery international Berlin : Springer, 1986 25(2009), 3 vom: 29. Jan., Seite 293-295 (DE-627)254638937 (DE-600)1463010-2 1437-9813 nnns volume:25 year:2009 number:3 day:29 month:01 pages:293-295 https://dx.doi.org/10.1007/s00383-009-2333-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.65 ASE 44.67 ASE AR 25 2009 3 29 01 293-295 |
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Enthalten in Pediatric surgery international 25(2009), 3 vom: 29. Jan., Seite 293-295 volume:25 year:2009 number:3 day:29 month:01 pages:293-295 |
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Enthalten in Pediatric surgery international 25(2009), 3 vom: 29. Jan., Seite 293-295 volume:25 year:2009 number:3 day:29 month:01 pages:293-295 |
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Nephroblastoma Teratoid Unilateral Histopathology |
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Pediatric surgery international |
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Gupta, Ruchika @@aut@@ Sharma, Alok @@aut@@ Arora, Raman @@aut@@ Dinda, Amit Kumar @@aut@@ |
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| author |
Gupta, Ruchika |
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Gupta, Ruchika ddc 610 bkl 44.65 bkl 44.67 misc Nephroblastoma misc Teratoid misc Unilateral misc Histopathology Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature |
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610 ASE 44.65 bkl 44.67 bkl Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature Nephroblastoma (dpeaa)DE-He213 Teratoid (dpeaa)DE-He213 Unilateral (dpeaa)DE-He213 Histopathology (dpeaa)DE-He213 |
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ddc 610 bkl 44.65 bkl 44.67 misc Nephroblastoma misc Teratoid misc Unilateral misc Histopathology |
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ddc 610 bkl 44.65 bkl 44.67 misc Nephroblastoma misc Teratoid misc Unilateral misc Histopathology |
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Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature |
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Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature |
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Gupta, Ruchika |
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stroma-predominant wilms tumor with teratoid features: report of a rare case and review of the literature |
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Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature |
| abstract |
Abstract We describe the case of a 4-year-old boy with a unilateral right-sided Wilms tumor with stromal predominance and teratoid features, which was localized to the kidney and hence, was completely resected. The pediatric surgeon and pathologist, both should be aware of this rare appearance of nephroblastoma so as to avoid the highly toxic chemotherapy and radiotherapy in such patients. |
| abstractGer |
Abstract We describe the case of a 4-year-old boy with a unilateral right-sided Wilms tumor with stromal predominance and teratoid features, which was localized to the kidney and hence, was completely resected. The pediatric surgeon and pathologist, both should be aware of this rare appearance of nephroblastoma so as to avoid the highly toxic chemotherapy and radiotherapy in such patients. |
| abstract_unstemmed |
Abstract We describe the case of a 4-year-old boy with a unilateral right-sided Wilms tumor with stromal predominance and teratoid features, which was localized to the kidney and hence, was completely resected. The pediatric surgeon and pathologist, both should be aware of this rare appearance of nephroblastoma so as to avoid the highly toxic chemotherapy and radiotherapy in such patients. |
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Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature |
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https://dx.doi.org/10.1007/s00383-009-2333-y |
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Sharma, Alok Arora, Raman Dinda, Amit Kumar |
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| doi_str |
10.1007/s00383-009-2333-y |
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2024-07-04T02:17:31.512Z |
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| score |
7.402815 |