The role of surgery in the treatment of neuroblastoma metastases at rare sites
Purpose Treatment of neuroblastoma metastases usually consists of chemotherapy and irradiation. However, in selected cases, surgical treatment is also indicated. In this study, we present three cases of patients with neuroblastoma metastases at rare sites that underwent surgery. Materials and method...
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Veröffentlicht in: | Journal of cancer research and clinical oncology 2023-11, Vol.149 (14), p.12913-12921 |
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creator | Scherer, Simon Mayer, Benjamin F. B. Dietzel, Markus Esser, Michael Warmann, Steven W. Lang, Peter Schuhmann, Martin U. Schmidt, Andreas Fuchs, Jörg |
description | Purpose
Treatment of neuroblastoma metastases usually consists of chemotherapy and irradiation. However, in selected cases, surgical treatment is also indicated. In this study, we present three cases of patients with neuroblastoma metastases at rare sites that underwent surgery.
Materials and methods
We retrospectively analyzed data of patients who underwent surgery for neuroblastoma at our department of Pediatric Surgery and Pediatric Urology at the University Children’s Hospital in Tuebingen and selected those patients who had surgery explicitly for a metastasis.
Results
Between 2002 and 2020, 277 children underwent surgical treatment for neuroblastoma. Three cases with metastases at exceptional sites are presented here after therapy according to protocols. One patient had a penile metastasis and received surgery including a plastic reconstruction. The patient showed no signs of erectile or urinary dysfunction at follow-up. Another patient had a metastasis in the proximal ulna, which remained vital even after exhausted treatment after two relapses. Afterward there was no restriction of movement of the extremity. The third patient had, amongst others, metastases to the pancreatic body and to the liver. Both were surgically removed during primary tumor resection. This patient died after local tumor relapse. The other two patients showed no evidence of tumor relapse after a follow-up of 18 and 17 months, respectively.
Conclusion
Although children with neuroblastoma often present with metastases, there is no recommendation for surgical treatment other than diagnostic biopsies. In case of persistence of metastasis or after exhaustion of high-risk therapy, surgical resection must be considered. |
doi_str_mv | 10.1007/s00432-023-05147-6 |
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Treatment of neuroblastoma metastases usually consists of chemotherapy and irradiation. However, in selected cases, surgical treatment is also indicated. In this study, we present three cases of patients with neuroblastoma metastases at rare sites that underwent surgery.
Materials and methods
We retrospectively analyzed data of patients who underwent surgery for neuroblastoma at our department of Pediatric Surgery and Pediatric Urology at the University Children’s Hospital in Tuebingen and selected those patients who had surgery explicitly for a metastasis.
Results
Between 2002 and 2020, 277 children underwent surgical treatment for neuroblastoma. Three cases with metastases at exceptional sites are presented here after therapy according to protocols. One patient had a penile metastasis and received surgery including a plastic reconstruction. The patient showed no signs of erectile or urinary dysfunction at follow-up. Another patient had a metastasis in the proximal ulna, which remained vital even after exhausted treatment after two relapses. Afterward there was no restriction of movement of the extremity. The third patient had, amongst others, metastases to the pancreatic body and to the liver. Both were surgically removed during primary tumor resection. This patient died after local tumor relapse. The other two patients showed no evidence of tumor relapse after a follow-up of 18 and 17 months, respectively.
Conclusion
Although children with neuroblastoma often present with metastases, there is no recommendation for surgical treatment other than diagnostic biopsies. In case of persistence of metastasis or after exhaustion of high-risk therapy, surgical resection must be considered.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-023-05147-6</identifier><identifier>PMID: 37466795</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Biopsy ; Cancer Research ; Chemotherapy ; Children ; Hematology ; Internal Medicine ; Medicine ; Medicine & Public Health ; Metastases ; Metastasis ; Neuroblastoma ; Oncology ; Patients ; Pediatrics ; Penis ; Reconstructive surgery ; Surgery ; Tumors</subject><ispartof>Journal of cancer research and clinical oncology, 2023-11, Vol.149 (14), p.12913-12921</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c426t-cb741fd8cb5f0bd49d44a8c95927a9765251a656c402cd313ca0395d162c66583</cites><orcidid>0000-0002-6404-6919</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00432-023-05147-6$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00432-023-05147-6$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37466795$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Scherer, Simon</creatorcontrib><creatorcontrib>Mayer, Benjamin F. B.</creatorcontrib><creatorcontrib>Dietzel, Markus</creatorcontrib><creatorcontrib>Esser, Michael</creatorcontrib><creatorcontrib>Warmann, Steven W.</creatorcontrib><creatorcontrib>Lang, Peter</creatorcontrib><creatorcontrib>Schuhmann, Martin U.</creatorcontrib><creatorcontrib>Schmidt, Andreas</creatorcontrib><creatorcontrib>Fuchs, Jörg</creatorcontrib><title>The role of surgery in the treatment of neuroblastoma metastases at rare sites</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><addtitle>J Cancer Res Clin Oncol</addtitle><description>Purpose
Treatment of neuroblastoma metastases usually consists of chemotherapy and irradiation. However, in selected cases, surgical treatment is also indicated. In this study, we present three cases of patients with neuroblastoma metastases at rare sites that underwent surgery.
Materials and methods
We retrospectively analyzed data of patients who underwent surgery for neuroblastoma at our department of Pediatric Surgery and Pediatric Urology at the University Children’s Hospital in Tuebingen and selected those patients who had surgery explicitly for a metastasis.
Results
Between 2002 and 2020, 277 children underwent surgical treatment for neuroblastoma. Three cases with metastases at exceptional sites are presented here after therapy according to protocols. One patient had a penile metastasis and received surgery including a plastic reconstruction. The patient showed no signs of erectile or urinary dysfunction at follow-up. Another patient had a metastasis in the proximal ulna, which remained vital even after exhausted treatment after two relapses. Afterward there was no restriction of movement of the extremity. The third patient had, amongst others, metastases to the pancreatic body and to the liver. Both were surgically removed during primary tumor resection. This patient died after local tumor relapse. The other two patients showed no evidence of tumor relapse after a follow-up of 18 and 17 months, respectively.
Conclusion
Although children with neuroblastoma often present with metastases, there is no recommendation for surgical treatment other than diagnostic biopsies. In case of persistence of metastasis or after exhaustion of high-risk therapy, surgical resection must be considered.</description><subject>Biopsy</subject><subject>Cancer Research</subject><subject>Chemotherapy</subject><subject>Children</subject><subject>Hematology</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Neuroblastoma</subject><subject>Oncology</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Penis</subject><subject>Reconstructive surgery</subject><subject>Surgery</subject><subject>Tumors</subject><issn>0171-5216</issn><issn>1432-1335</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kUtPxCAUhYnR6Pj4Ay4MiRs3Vd6UlTETX4nRzbgmlFKtaYsCNfHfSx0dHwtXwD0f596bA8A-RscYIXkSEWKUFIjQAnHMZCHWwAxPJUwpXwczhCUuOMFiC2zH-ITym0uyCbaoZEJIxWfgdvHoYPCdg76BcQwPLrzBdoApl1NwJvVuSJM2uDH4qjMx-d7A3qV8M9FFaBIMJjgY2-TiLthoTBfd3ue5A-4vzhfzq-Lm7vJ6fnZTWEZEKmwlGW7q0la8QVXNVM2YKa3iikijpOCEYyO4sAwRW1NMrUFU8RoLYoXgJd0Bp0vf57HqXW3zkMF0-jm0vQlv2ptW_1aG9lE_-FeNES8lUpPD0adD8C-ji0n3bbSu68zg_Bg1KamSLNMio4d_0Cc_hiHvlylZKswZJ5kiS8oGH2NwzWoajPSUl17mpXNe-iMvPVkf_Nxj9eUroAzQJRCzNOR0vnv_Y_sO3Caghg</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Scherer, Simon</creator><creator>Mayer, Benjamin F. B.</creator><creator>Dietzel, Markus</creator><creator>Esser, Michael</creator><creator>Warmann, Steven W.</creator><creator>Lang, Peter</creator><creator>Schuhmann, Martin U.</creator><creator>Schmidt, Andreas</creator><creator>Fuchs, Jörg</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6404-6919</orcidid></search><sort><creationdate>20231101</creationdate><title>The role of surgery in the treatment of neuroblastoma metastases at rare sites</title><author>Scherer, Simon ; Mayer, Benjamin F. B. ; Dietzel, Markus ; Esser, Michael ; Warmann, Steven W. ; Lang, Peter ; Schuhmann, Martin U. ; Schmidt, Andreas ; Fuchs, Jörg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-cb741fd8cb5f0bd49d44a8c95927a9765251a656c402cd313ca0395d162c66583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biopsy</topic><topic>Cancer Research</topic><topic>Chemotherapy</topic><topic>Children</topic><topic>Hematology</topic><topic>Internal Medicine</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Neuroblastoma</topic><topic>Oncology</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Penis</topic><topic>Reconstructive surgery</topic><topic>Surgery</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scherer, Simon</creatorcontrib><creatorcontrib>Mayer, Benjamin F. B.</creatorcontrib><creatorcontrib>Dietzel, Markus</creatorcontrib><creatorcontrib>Esser, Michael</creatorcontrib><creatorcontrib>Warmann, Steven W.</creatorcontrib><creatorcontrib>Lang, Peter</creatorcontrib><creatorcontrib>Schuhmann, Martin U.</creatorcontrib><creatorcontrib>Schmidt, Andreas</creatorcontrib><creatorcontrib>Fuchs, Jörg</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</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>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cancer research and clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scherer, Simon</au><au>Mayer, Benjamin F. B.</au><au>Dietzel, Markus</au><au>Esser, Michael</au><au>Warmann, Steven W.</au><au>Lang, Peter</au><au>Schuhmann, Martin U.</au><au>Schmidt, Andreas</au><au>Fuchs, Jörg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of surgery in the treatment of neuroblastoma metastases at rare sites</atitle><jtitle>Journal of cancer research and clinical oncology</jtitle><stitle>J Cancer Res Clin Oncol</stitle><addtitle>J Cancer Res Clin Oncol</addtitle><date>2023-11-01</date><risdate>2023</risdate><volume>149</volume><issue>14</issue><spage>12913</spage><epage>12921</epage><pages>12913-12921</pages><issn>0171-5216</issn><eissn>1432-1335</eissn><abstract>Purpose
Treatment of neuroblastoma metastases usually consists of chemotherapy and irradiation. However, in selected cases, surgical treatment is also indicated. In this study, we present three cases of patients with neuroblastoma metastases at rare sites that underwent surgery.
Materials and methods
We retrospectively analyzed data of patients who underwent surgery for neuroblastoma at our department of Pediatric Surgery and Pediatric Urology at the University Children’s Hospital in Tuebingen and selected those patients who had surgery explicitly for a metastasis.
Results
Between 2002 and 2020, 277 children underwent surgical treatment for neuroblastoma. Three cases with metastases at exceptional sites are presented here after therapy according to protocols. One patient had a penile metastasis and received surgery including a plastic reconstruction. The patient showed no signs of erectile or urinary dysfunction at follow-up. Another patient had a metastasis in the proximal ulna, which remained vital even after exhausted treatment after two relapses. Afterward there was no restriction of movement of the extremity. The third patient had, amongst others, metastases to the pancreatic body and to the liver. Both were surgically removed during primary tumor resection. This patient died after local tumor relapse. The other two patients showed no evidence of tumor relapse after a follow-up of 18 and 17 months, respectively.
Conclusion
Although children with neuroblastoma often present with metastases, there is no recommendation for surgical treatment other than diagnostic biopsies. In case of persistence of metastasis or after exhaustion of high-risk therapy, surgical resection must be considered.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37466795</pmid><doi>10.1007/s00432-023-05147-6</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6404-6919</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biopsy Cancer Research Chemotherapy Children Hematology Internal Medicine Medicine Medicine & Public Health Metastases Metastasis Neuroblastoma Oncology Patients Pediatrics Penis Reconstructive surgery Surgery Tumors |
title | The role of surgery in the treatment of neuroblastoma metastases at rare sites |
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