Partial nephrectomy in a cystic partially differentiated nephroblastoma
Cystic partially differentiated nephroblastoma (CPDN) is a rare neoplastic disorder consisting of a well‐demarcated cystic lesion of the kidney where blasternal or other embryonic cells are present in the septa of the cysts. Magnetic resonance imaging can detect the cystic character of the lesion an...
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Veröffentlicht in: | Medical and pediatric oncology 1997-06, Vol.28 (6), p.416-419 |
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creator | Streif, Werner Gassner, Ingmar Janetschek, Günther Kreczy, Alfons Judmaier, Werner Fink, Franz-Martin |
description | Cystic partially differentiated nephroblastoma (CPDN) is a rare neoplastic disorder consisting of a well‐demarcated cystic lesion of the kidney where blasternal or other embryonic cells are present in the septa of the cysts. Magnetic resonance imaging can detect the cystic character of the lesion and will produce imaging features that are highly suggestive of either CPDN or cystic nephroma (CN) (synonym: multilocular cyst of the kidney), a benign entity. Although malignant potential exists in CPDN, all cases reported to date have had a favorable prognosis after surgery alone. Partial nephrectomy is considered safe, and the treatment of choice in the newborn period. We report a case of CPDN in a newborn that was successfully treated with partial nephrectomy. More than five years after nephron sparing surgery, the involved kidney shows normal anatomical structure except for a diminished upper pole, no evidence of tumor recurrence and good renal function. Med. Pediatr. Oncol. 28:416–419, 1997. © 1997 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1096-911X(199706)28:6<416::AID-MPO4>3.0.CO;2-J |
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Magnetic resonance imaging can detect the cystic character of the lesion and will produce imaging features that are highly suggestive of either CPDN or cystic nephroma (CN) (synonym: multilocular cyst of the kidney), a benign entity. Although malignant potential exists in CPDN, all cases reported to date have had a favorable prognosis after surgery alone. Partial nephrectomy is considered safe, and the treatment of choice in the newborn period. We report a case of CPDN in a newborn that was successfully treated with partial nephrectomy. More than five years after nephron sparing surgery, the involved kidney shows normal anatomical structure except for a diminished upper pole, no evidence of tumor recurrence and good renal function. Med. Pediatr. Oncol. 28:416–419, 1997. © 1997 Wiley‐Liss, Inc.</description><identifier>ISSN: 0098-1532</identifier><identifier>EISSN: 1096-911X</identifier><identifier>DOI: 10.1002/(SICI)1096-911X(199706)28:6<416::AID-MPO4>3.0.CO;2-J</identifier><identifier>PMID: 9143385</identifier><identifier>CODEN: MPONDB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; cystic partially differentiated nephroblastoma ; cystic renal tumors ; Cysts - pathology ; Cysts - surgery ; Diagnosis, Differential ; Humans ; infant ; Infant, Newborn ; Kidney Neoplasms - pathology ; Kidney Neoplasms - surgery ; Kidneys ; Medical sciences ; Nephrectomy - methods ; Nephrology. 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Pediatr. Oncol</addtitle><description>Cystic partially differentiated nephroblastoma (CPDN) is a rare neoplastic disorder consisting of a well‐demarcated cystic lesion of the kidney where blasternal or other embryonic cells are present in the septa of the cysts. Magnetic resonance imaging can detect the cystic character of the lesion and will produce imaging features that are highly suggestive of either CPDN or cystic nephroma (CN) (synonym: multilocular cyst of the kidney), a benign entity. Although malignant potential exists in CPDN, all cases reported to date have had a favorable prognosis after surgery alone. Partial nephrectomy is considered safe, and the treatment of choice in the newborn period. We report a case of CPDN in a newborn that was successfully treated with partial nephrectomy. More than five years after nephron sparing surgery, the involved kidney shows normal anatomical structure except for a diminished upper pole, no evidence of tumor recurrence and good renal function. Med. Pediatr. Oncol. 28:416–419, 1997. © 1997 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>cystic partially differentiated nephroblastoma</subject><subject>cystic renal tumors</subject><subject>Cysts - pathology</subject><subject>Cysts - surgery</subject><subject>Diagnosis, Differential</subject><subject>Humans</subject><subject>infant</subject><subject>Infant, Newborn</subject><subject>Kidney Neoplasms - pathology</subject><subject>Kidney Neoplasms - surgery</subject><subject>Kidneys</subject><subject>Medical sciences</subject><subject>Nephrectomy - methods</subject><subject>Nephrology. Urinary tract diseases</subject><subject>newborn</subject><subject>Tumors of the urinary system</subject><subject>Wilms Tumor - pathology</subject><subject>Wilms Tumor - surgery</subject><issn>0098-1532</issn><issn>1096-911X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF1v0zAYhS0EGmXwE5BygdB2keKPxI7LhLQFKC2jrbQhuHvlOLbISJPOTgX59zikKhcgcWUdveccHz0IXRA8JRjTV2c3i3xxTrDksSTk6xmRUmB-TrMZv0gIn80uF2_jT5t18oZN8TRfv6bx8gGaHAMP0QRjmcUkZfQxeuL9HQ5aiuwEnUiSMJalEzTfKNdVqo4as_vmjO7abR9VTaQi3fuu0tFuvNd9VFbWGmeaIDtTjoG2qJUPGfUUPbKq9ubZ4T1Fn9-_u80_xNfr-SK_vI51QkUSlybjylqaSaqTEjNOSkwlw7iwNs1KYzihxGqRFaXWheKCSUxSaVJcWlZQwU7Ry7F359r7vfEdbCuvTV2rxrR7DyKTIhGUBePtaNSu9d4ZCztXbZXrgWAY-AIMfGHABQMuGPkCzYBD4AsQ-MLAFxhgyNdAYRlqnx_-3xdbUx5LD0DD_cXhrrxWtXWq0ZU_2igXQjLyZ92Pqjb9X9P-s-wfw37rUBuPtZXvzM9jrXLfIaAUKXxZzWGzXN2srshHwOwXGTayeg</recordid><startdate>199706</startdate><enddate>199706</enddate><creator>Streif, Werner</creator><creator>Gassner, Ingmar</creator><creator>Janetschek, Günther</creator><creator>Kreczy, Alfons</creator><creator>Judmaier, Werner</creator><creator>Fink, Franz-Martin</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199706</creationdate><title>Partial nephrectomy in a cystic partially differentiated nephroblastoma</title><author>Streif, Werner ; Gassner, Ingmar ; Janetschek, Günther ; Kreczy, Alfons ; Judmaier, Werner ; Fink, Franz-Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4274-de86aff2892c4d0361d029300bff58dee6121fc78bdccba67390159e50df3b273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Biological and medical sciences</topic><topic>cystic partially differentiated nephroblastoma</topic><topic>cystic renal tumors</topic><topic>Cysts - pathology</topic><topic>Cysts - surgery</topic><topic>Diagnosis, Differential</topic><topic>Humans</topic><topic>infant</topic><topic>Infant, Newborn</topic><topic>Kidney Neoplasms - pathology</topic><topic>Kidney Neoplasms - surgery</topic><topic>Kidneys</topic><topic>Medical sciences</topic><topic>Nephrectomy - methods</topic><topic>Nephrology. Urinary tract diseases</topic><topic>newborn</topic><topic>Tumors of the urinary system</topic><topic>Wilms Tumor - pathology</topic><topic>Wilms Tumor - surgery</topic><toplevel>online_resources</toplevel><creatorcontrib>Streif, Werner</creatorcontrib><creatorcontrib>Gassner, Ingmar</creatorcontrib><creatorcontrib>Janetschek, Günther</creatorcontrib><creatorcontrib>Kreczy, Alfons</creatorcontrib><creatorcontrib>Judmaier, Werner</creatorcontrib><creatorcontrib>Fink, Franz-Martin</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Medical and pediatric oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Streif, Werner</au><au>Gassner, Ingmar</au><au>Janetschek, Günther</au><au>Kreczy, Alfons</au><au>Judmaier, Werner</au><au>Fink, Franz-Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Partial nephrectomy in a cystic partially differentiated nephroblastoma</atitle><jtitle>Medical and pediatric oncology</jtitle><addtitle>Med. 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We report a case of CPDN in a newborn that was successfully treated with partial nephrectomy. More than five years after nephron sparing surgery, the involved kidney shows normal anatomical structure except for a diminished upper pole, no evidence of tumor recurrence and good renal function. Med. Pediatr. Oncol. 28:416–419, 1997. © 1997 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9143385</pmid><doi>10.1002/(SICI)1096-911X(199706)28:6<416::AID-MPO4>3.0.CO;2-J</doi><tpages>4</tpages></addata></record> |
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subjects | Biological and medical sciences cystic partially differentiated nephroblastoma cystic renal tumors Cysts - pathology Cysts - surgery Diagnosis, Differential Humans infant Infant, Newborn Kidney Neoplasms - pathology Kidney Neoplasms - surgery Kidneys Medical sciences Nephrectomy - methods Nephrology. Urinary tract diseases newborn Tumors of the urinary system Wilms Tumor - pathology Wilms Tumor - surgery |
title | Partial nephrectomy in a cystic partially differentiated nephroblastoma |
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