Sacrococcygeal teratoma
This retrospective study details our experience regarding 72 patients with sacrococcygeal teratoma treated over a period of 17 years. The sex incidence was nearly equal, but there was a high proportion of Altmann type IV tumors. A preliminary colostomy before combined abdominosacral excision of larg...
Gespeichert in:
Veröffentlicht in: | Pediatric surgery international 2002-09, Vol.18 (5-6), p.384-387 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 387 |
---|---|
container_issue | 5-6 |
container_start_page | 384 |
container_title | Pediatric surgery international |
container_volume | 18 |
creator | WAKHLU, Ashish MISRA, Sanjeev TANDON, R. K WAKHLU, A. K |
description | This retrospective study details our experience regarding 72 patients with sacrococcygeal teratoma treated over a period of 17 years. The sex incidence was nearly equal, but there was a high proportion of Altmann type IV tumors. A preliminary colostomy before combined abdominosacral excision of large type III and IV lesions reduced morbidity. Sixty-six percent of the patients presented beyond the neonatal period; 14 had been treated elsewhere for bowel/urinary obstruction. Imaging studies included radiography, abdominal ultrasound, computed tomography, and magnetic resonance imaging (after 1995). In 60 patients the tumor was excised via the sacral route, 11 had a preliminary colostomy, and 1 had a vesicostomy. Eight children (5 with malignant lesions) required abdominosacral excision. After 1990, serial estimation of serum alpha-fetoprotein (AFP) was used to monitor tumor recurrence. There were 34 male and 38 female patients (age range 3 days-12 years); 47 had benign tumors, of which 42 were excised through the sacral route. Three patients underwent a preliminary colostomy and abdominosacral excision of the tumor with subsequent colostomy closure. There were 4 deaths in this group; no recurrence was seen in the surviving children with benign tumors. Twenty-five patients had malignant teratomas. In 18 of these the tumor was excised via the sacral route and 5 underwent abdominal-sacral excision. Eight had a preliminary colostomy and chemotherapy followed by excision of the residual tumor and colostomy closure. None of the initial 14 patients with malignant lesions survived beyond 2 years. Of the latter 11 (who received cisplatinum-based chemotherapy), 10 were alive 1 year after surgery. One patient is currently on preoperative chemotherapy and another developed recurrence of the tumor. The overall follow-up ranged from 3 months to 8 years; there has been no complaint of functional neurological deficit in any of the patients. As intrapelvic tumors tend to have a delayed diagnosis, this can be avoided by performing a rectal examination. There should be no recurrence after excision of a benign teratoma. Cisplatinum-based chemotherapy has improved the survival of patients with malignant tumors. |
doi_str_mv | 10.1007/s00383-002-0729-z |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_220141505</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1316860761</sourcerecordid><originalsourceid>FETCH-LOGICAL-c354t-11b08800a1d183c829328ffb8089638ede1965c7a648d163da730e1c8496ae2d3</originalsourceid><addsrcrecordid>eNpFkE1LAzEQhoMotlbP4kVE8BidySTZ5CjFLyh4UM8hzWalpe3WZHtof70pXehpLs_7MS9jNwiPCFA9ZQAyxAEEh0pYvjthQ5RUcWuQTtkQsLIcSJkBu8h5DgCGtD1nAxQSFWkcsusvH1Ib2hC2v9Ev7rqYfNcu_SU7a_wix6v-jtjP68v3-J1PPt8-xs8THkjJjiNOwRgAjzUaCkZYEqZppgaM1WRiHdFqFSqvpalRU-0rgojBSKt9FDWN2P3Bd53av03MnZu3m7QqkU4IwFITVIHwAJWqOafYuHWaLX3aOgS3X8IdlnBlCbdfwu2K5rY33kyXsT4q-tcL8NADPge_aJJfhVk-crKkK6noH8gVYzo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>220141505</pqid></control><display><type>article</type><title>Sacrococcygeal teratoma</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>WAKHLU, Ashish ; MISRA, Sanjeev ; TANDON, R. K ; WAKHLU, A. K</creator><creatorcontrib>WAKHLU, Ashish ; MISRA, Sanjeev ; TANDON, R. K ; WAKHLU, A. K</creatorcontrib><description>This retrospective study details our experience regarding 72 patients with sacrococcygeal teratoma treated over a period of 17 years. The sex incidence was nearly equal, but there was a high proportion of Altmann type IV tumors. A preliminary colostomy before combined abdominosacral excision of large type III and IV lesions reduced morbidity. Sixty-six percent of the patients presented beyond the neonatal period; 14 had been treated elsewhere for bowel/urinary obstruction. Imaging studies included radiography, abdominal ultrasound, computed tomography, and magnetic resonance imaging (after 1995). In 60 patients the tumor was excised via the sacral route, 11 had a preliminary colostomy, and 1 had a vesicostomy. Eight children (5 with malignant lesions) required abdominosacral excision. After 1990, serial estimation of serum alpha-fetoprotein (AFP) was used to monitor tumor recurrence. There were 34 male and 38 female patients (age range 3 days-12 years); 47 had benign tumors, of which 42 were excised through the sacral route. Three patients underwent a preliminary colostomy and abdominosacral excision of the tumor with subsequent colostomy closure. There were 4 deaths in this group; no recurrence was seen in the surviving children with benign tumors. Twenty-five patients had malignant teratomas. In 18 of these the tumor was excised via the sacral route and 5 underwent abdominal-sacral excision. Eight had a preliminary colostomy and chemotherapy followed by excision of the residual tumor and colostomy closure. None of the initial 14 patients with malignant lesions survived beyond 2 years. Of the latter 11 (who received cisplatinum-based chemotherapy), 10 were alive 1 year after surgery. One patient is currently on preoperative chemotherapy and another developed recurrence of the tumor. The overall follow-up ranged from 3 months to 8 years; there has been no complaint of functional neurological deficit in any of the patients. As intrapelvic tumors tend to have a delayed diagnosis, this can be avoided by performing a rectal examination. There should be no recurrence after excision of a benign teratoma. Cisplatinum-based chemotherapy has improved the survival of patients with malignant tumors.</description><identifier>ISSN: 0179-0358</identifier><identifier>EISSN: 1437-9813</identifier><identifier>DOI: 10.1007/s00383-002-0729-z</identifier><identifier>PMID: 12415361</identifier><identifier>CODEN: PSUIED</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Adolescent ; Biological and medical sciences ; Child ; Child, Preschool ; Combined Modality Therapy ; Diseases of the osteoarticular system ; Female ; Humans ; Infant ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Retrospective Studies ; Sacrococcygeal Region ; Teratoma - diagnosis ; Teratoma - surgery ; Tumors of striated muscle and skeleton</subject><ispartof>Pediatric surgery international, 2002-09, Vol.18 (5-6), p.384-387</ispartof><rights>2003 INIST-CNRS</rights><rights>2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-11b08800a1d183c829328ffb8089638ede1965c7a648d163da730e1c8496ae2d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14014545$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12415361$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WAKHLU, Ashish</creatorcontrib><creatorcontrib>MISRA, Sanjeev</creatorcontrib><creatorcontrib>TANDON, R. K</creatorcontrib><creatorcontrib>WAKHLU, A. K</creatorcontrib><title>Sacrococcygeal teratoma</title><title>Pediatric surgery international</title><addtitle>Pediatr Surg Int</addtitle><description>This retrospective study details our experience regarding 72 patients with sacrococcygeal teratoma treated over a period of 17 years. The sex incidence was nearly equal, but there was a high proportion of Altmann type IV tumors. A preliminary colostomy before combined abdominosacral excision of large type III and IV lesions reduced morbidity. Sixty-six percent of the patients presented beyond the neonatal period; 14 had been treated elsewhere for bowel/urinary obstruction. Imaging studies included radiography, abdominal ultrasound, computed tomography, and magnetic resonance imaging (after 1995). In 60 patients the tumor was excised via the sacral route, 11 had a preliminary colostomy, and 1 had a vesicostomy. Eight children (5 with malignant lesions) required abdominosacral excision. After 1990, serial estimation of serum alpha-fetoprotein (AFP) was used to monitor tumor recurrence. There were 34 male and 38 female patients (age range 3 days-12 years); 47 had benign tumors, of which 42 were excised through the sacral route. Three patients underwent a preliminary colostomy and abdominosacral excision of the tumor with subsequent colostomy closure. There were 4 deaths in this group; no recurrence was seen in the surviving children with benign tumors. Twenty-five patients had malignant teratomas. In 18 of these the tumor was excised via the sacral route and 5 underwent abdominal-sacral excision. Eight had a preliminary colostomy and chemotherapy followed by excision of the residual tumor and colostomy closure. None of the initial 14 patients with malignant lesions survived beyond 2 years. Of the latter 11 (who received cisplatinum-based chemotherapy), 10 were alive 1 year after surgery. One patient is currently on preoperative chemotherapy and another developed recurrence of the tumor. The overall follow-up ranged from 3 months to 8 years; there has been no complaint of functional neurological deficit in any of the patients. As intrapelvic tumors tend to have a delayed diagnosis, this can be avoided by performing a rectal examination. There should be no recurrence after excision of a benign teratoma. Cisplatinum-based chemotherapy has improved the survival of patients with malignant tumors.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Combined Modality Therapy</subject><subject>Diseases of the osteoarticular system</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Retrospective Studies</subject><subject>Sacrococcygeal Region</subject><subject>Teratoma - diagnosis</subject><subject>Teratoma - surgery</subject><subject>Tumors of striated muscle and skeleton</subject><issn>0179-0358</issn><issn>1437-9813</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpFkE1LAzEQhoMotlbP4kVE8BidySTZ5CjFLyh4UM8hzWalpe3WZHtof70pXehpLs_7MS9jNwiPCFA9ZQAyxAEEh0pYvjthQ5RUcWuQTtkQsLIcSJkBu8h5DgCGtD1nAxQSFWkcsusvH1Ib2hC2v9Ev7rqYfNcu_SU7a_wix6v-jtjP68v3-J1PPt8-xs8THkjJjiNOwRgAjzUaCkZYEqZppgaM1WRiHdFqFSqvpalRU-0rgojBSKt9FDWN2P3Bd53av03MnZu3m7QqkU4IwFITVIHwAJWqOafYuHWaLX3aOgS3X8IdlnBlCbdfwu2K5rY33kyXsT4q-tcL8NADPge_aJJfhVk-crKkK6noH8gVYzo</recordid><startdate>20020901</startdate><enddate>20020901</enddate><creator>WAKHLU, Ashish</creator><creator>MISRA, Sanjeev</creator><creator>TANDON, R. K</creator><creator>WAKHLU, A. K</creator><general>Springer</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20020901</creationdate><title>Sacrococcygeal teratoma</title><author>WAKHLU, Ashish ; MISRA, Sanjeev ; TANDON, R. K ; WAKHLU, A. K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-11b08800a1d183c829328ffb8089638ede1965c7a648d163da730e1c8496ae2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Combined Modality Therapy</topic><topic>Diseases of the osteoarticular system</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Retrospective Studies</topic><topic>Sacrococcygeal Region</topic><topic>Teratoma - diagnosis</topic><topic>Teratoma - surgery</topic><topic>Tumors of striated muscle and skeleton</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WAKHLU, Ashish</creatorcontrib><creatorcontrib>MISRA, Sanjeev</creatorcontrib><creatorcontrib>TANDON, R. K</creatorcontrib><creatorcontrib>WAKHLU, A. K</creatorcontrib><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>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Pediatric surgery international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WAKHLU, Ashish</au><au>MISRA, Sanjeev</au><au>TANDON, R. K</au><au>WAKHLU, A. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sacrococcygeal teratoma</atitle><jtitle>Pediatric surgery international</jtitle><addtitle>Pediatr Surg Int</addtitle><date>2002-09-01</date><risdate>2002</risdate><volume>18</volume><issue>5-6</issue><spage>384</spage><epage>387</epage><pages>384-387</pages><issn>0179-0358</issn><eissn>1437-9813</eissn><coden>PSUIED</coden><abstract>This retrospective study details our experience regarding 72 patients with sacrococcygeal teratoma treated over a period of 17 years. The sex incidence was nearly equal, but there was a high proportion of Altmann type IV tumors. A preliminary colostomy before combined abdominosacral excision of large type III and IV lesions reduced morbidity. Sixty-six percent of the patients presented beyond the neonatal period; 14 had been treated elsewhere for bowel/urinary obstruction. Imaging studies included radiography, abdominal ultrasound, computed tomography, and magnetic resonance imaging (after 1995). In 60 patients the tumor was excised via the sacral route, 11 had a preliminary colostomy, and 1 had a vesicostomy. Eight children (5 with malignant lesions) required abdominosacral excision. After 1990, serial estimation of serum alpha-fetoprotein (AFP) was used to monitor tumor recurrence. There were 34 male and 38 female patients (age range 3 days-12 years); 47 had benign tumors, of which 42 were excised through the sacral route. Three patients underwent a preliminary colostomy and abdominosacral excision of the tumor with subsequent colostomy closure. There were 4 deaths in this group; no recurrence was seen in the surviving children with benign tumors. Twenty-five patients had malignant teratomas. In 18 of these the tumor was excised via the sacral route and 5 underwent abdominal-sacral excision. Eight had a preliminary colostomy and chemotherapy followed by excision of the residual tumor and colostomy closure. None of the initial 14 patients with malignant lesions survived beyond 2 years. Of the latter 11 (who received cisplatinum-based chemotherapy), 10 were alive 1 year after surgery. One patient is currently on preoperative chemotherapy and another developed recurrence of the tumor. The overall follow-up ranged from 3 months to 8 years; there has been no complaint of functional neurological deficit in any of the patients. As intrapelvic tumors tend to have a delayed diagnosis, this can be avoided by performing a rectal examination. There should be no recurrence after excision of a benign teratoma. Cisplatinum-based chemotherapy has improved the survival of patients with malignant tumors.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><pub>Springer</pub><pmid>12415361</pmid><doi>10.1007/s00383-002-0729-z</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0179-0358 |
ispartof | Pediatric surgery international, 2002-09, Vol.18 (5-6), p.384-387 |
issn | 0179-0358 1437-9813 |
language | eng |
recordid | cdi_proquest_journals_220141505 |
source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Adolescent Biological and medical sciences Child Child, Preschool Combined Modality Therapy Diseases of the osteoarticular system Female Humans Infant Magnetic Resonance Imaging Male Medical sciences Retrospective Studies Sacrococcygeal Region Teratoma - diagnosis Teratoma - surgery Tumors of striated muscle and skeleton |
title | Sacrococcygeal teratoma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T00%3A48%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sacrococcygeal%20teratoma&rft.jtitle=Pediatric%20surgery%20international&rft.au=WAKHLU,%20Ashish&rft.date=2002-09-01&rft.volume=18&rft.issue=5-6&rft.spage=384&rft.epage=387&rft.pages=384-387&rft.issn=0179-0358&rft.eissn=1437-9813&rft.coden=PSUIED&rft_id=info:doi/10.1007/s00383-002-0729-z&rft_dat=%3Cproquest_cross%3E1316860761%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=220141505&rft_id=info:pmid/12415361&rfr_iscdi=true |