Diagnostic and therapeutic problems of soft tissue tumors other than rhabdomyosarcoma in infants under 1 year of age: A clinicopathological study of 34 cases treated at the institut gustave-roussy
Thirty‐four cases of soft tissue tumors (STT) other than rhabdomyosarcoma in infants under 1 year of age were seen in our institution between 1955 and 1985. All were diagnosed initially as malignant tumors except for three cases of fibromatosis, and, thus, they received therapy appropriate at that t...
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Veröffentlicht in: | Medical and pediatric oncology 1990, Vol.18 (1), p.37-43 |
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creator | Salloum, Emile Flamant, Françoise Caillaud, Jean M. Friedman, Samuel Wacker, Pierre Coppes, Max J. Brugieres, Laurence Lemerle, Jean |
description | Thirty‐four cases of soft tissue tumors (STT) other than rhabdomyosarcoma in infants under 1 year of age were seen in our institution between 1955 and 1985. All were diagnosed initially as malignant tumors except for three cases of fibromatosis, and, thus, they received therapy appropriate at that time. During a recent pathologic review, four were seen to have had hemangioma, six hemangiopericytoma, one hamartoma, seven fibromatosis, eight fibrosarcoma, and eight unclassified sarcomas. Of these 34 cases, the initial histological diagnosis was confirmed in only 17. Sixteen patients were believed to have received inappropriately aggressive therapy; indeed, four of these cases diagnosed prior to 1975 had been benign. Major long‐term side effects were seen in 7/16 treated patients (six radiotherapy, one surgery), who, in retrospect, should have received less aggressive treatment.
The reasons for these initial errors in diagnosis included doubtful histologic features associated in some cases with alarming clinical presentation. We believe that difficulties still remain in distinguishing benign from malignant STT in this age group by histological examination. Therefore, we urge extreme caution in using aggressive therapy before the diagnosis is certain. |
doi_str_mv | 10.1002/mpo.2950180108 |
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The reasons for these initial errors in diagnosis included doubtful histologic features associated in some cases with alarming clinical presentation. We believe that difficulties still remain in distinguishing benign from malignant STT in this age group by histological examination. Therefore, we urge extreme caution in using aggressive therapy before the diagnosis is certain.</description><identifier>ISSN: 0098-1532</identifier><identifier>EISSN: 1096-911X</identifier><identifier>DOI: 10.1002/mpo.2950180108</identifier><identifier>PMID: 2294390</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Age Factors ; Diagnosis, Differential ; Female ; Fibroma - pathology ; fibrosarcoma ; Fibrosarcoma - pathology ; Hemangioma - pathology ; hemangiopericytoma ; Hemangiopericytoma - pathology ; Humans ; Infant ; Infant, Newborn ; Male ; Neoplasm Recurrence, Local ; Sarcoma - pathology ; Soft Tissue Neoplasms - diagnosis ; Soft Tissue Neoplasms - pathology ; Soft Tissue Neoplasms - therapy ; unclassified sarcoma</subject><ispartof>Medical and pediatric oncology, 1990, Vol.18 (1), p.37-43</ispartof><rights>Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3788-e63037313c2a6bd83269954d66415ee129f49dfa944b03861c22ba63d02b6cf3</citedby><cites>FETCH-LOGICAL-c3788-e63037313c2a6bd83269954d66415ee129f49dfa944b03861c22ba63d02b6cf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmpo.2950180108$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmpo.2950180108$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,4024,27923,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2294390$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Salloum, Emile</creatorcontrib><creatorcontrib>Flamant, Françoise</creatorcontrib><creatorcontrib>Caillaud, Jean M.</creatorcontrib><creatorcontrib>Friedman, Samuel</creatorcontrib><creatorcontrib>Wacker, Pierre</creatorcontrib><creatorcontrib>Coppes, Max J.</creatorcontrib><creatorcontrib>Brugieres, Laurence</creatorcontrib><creatorcontrib>Lemerle, Jean</creatorcontrib><title>Diagnostic and therapeutic problems of soft tissue tumors other than rhabdomyosarcoma in infants under 1 year of age: A clinicopathological study of 34 cases treated at the institut gustave-roussy</title><title>Medical and pediatric oncology</title><addtitle>Med. Pediatr. Oncol</addtitle><description>Thirty‐four cases of soft tissue tumors (STT) other than rhabdomyosarcoma in infants under 1 year of age were seen in our institution between 1955 and 1985. All were diagnosed initially as malignant tumors except for three cases of fibromatosis, and, thus, they received therapy appropriate at that time. During a recent pathologic review, four were seen to have had hemangioma, six hemangiopericytoma, one hamartoma, seven fibromatosis, eight fibrosarcoma, and eight unclassified sarcomas. Of these 34 cases, the initial histological diagnosis was confirmed in only 17. Sixteen patients were believed to have received inappropriately aggressive therapy; indeed, four of these cases diagnosed prior to 1975 had been benign. Major long‐term side effects were seen in 7/16 treated patients (six radiotherapy, one surgery), who, in retrospect, should have received less aggressive treatment.
The reasons for these initial errors in diagnosis included doubtful histologic features associated in some cases with alarming clinical presentation. We believe that difficulties still remain in distinguishing benign from malignant STT in this age group by histological examination. Therefore, we urge extreme caution in using aggressive therapy before the diagnosis is certain.</description><subject>Age Factors</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Fibroma - pathology</subject><subject>fibrosarcoma</subject><subject>Fibrosarcoma - pathology</subject><subject>Hemangioma - pathology</subject><subject>hemangiopericytoma</subject><subject>Hemangiopericytoma - pathology</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Neoplasm Recurrence, Local</subject><subject>Sarcoma - pathology</subject><subject>Soft Tissue Neoplasms - diagnosis</subject><subject>Soft Tissue Neoplasms - pathology</subject><subject>Soft Tissue Neoplasms - therapy</subject><subject>unclassified sarcoma</subject><issn>0098-1532</issn><issn>1096-911X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUhSMEKkNhyw7JK3YZ_JM4MbtSoKUqlEUlEBvrxnFmDEkcfB0g78eD4WhGRayQLFnX95xPRz5Z9pTRLaOUvxgmv-WqpKymjNb3sg2jSuaKsc_3sw2lqs5ZKfjD7BHiV5pmVdUn2QnnqhCKbrLfrx3sRo_RGQJjS-LeBpjsvM5T8E1vByS-I-i7SKJDnC2J8-BDel21yQAjCXtoWj8sHiEYPwBxYzodjBHJPLZJxshiIawk2NmX5IyY3o3O-Ani3vd-5wz0BOPcLqtGFMQAWiQxWIi2JRDXZImZgsY5kt2MEX7YPPgZcXmcPeigR_vkeJ9mt2_f3J5f5tc3F-_Oz65zI6q6zq0UVFSCCcNBNm0tuFSqLFopC1Zay7jqCtV2oIqioaKWzHDegBQt5Y00nTjNnh-w6WO-zxajHhwa2_cw2pRDV6oURSnrJNwehCZ4xGA7PQU3QFg0o3ptTafW9N_WkuHZkTw3g23v5Mea0l4d9j9db5f_0PT7jzf_sPOD12G0v-68EL5pWYmq1J8-XOgv_Oqyuiq4fiX-AEAKtwk</recordid><startdate>1990</startdate><enddate>1990</enddate><creator>Salloum, Emile</creator><creator>Flamant, Françoise</creator><creator>Caillaud, Jean M.</creator><creator>Friedman, Samuel</creator><creator>Wacker, Pierre</creator><creator>Coppes, Max J.</creator><creator>Brugieres, Laurence</creator><creator>Lemerle, Jean</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>1990</creationdate><title>Diagnostic and therapeutic problems of soft tissue tumors other than rhabdomyosarcoma in infants under 1 year of age: A clinicopathological study of 34 cases treated at the institut gustave-roussy</title><author>Salloum, Emile ; Flamant, Françoise ; Caillaud, Jean M. ; Friedman, Samuel ; Wacker, Pierre ; Coppes, Max J. ; Brugieres, Laurence ; Lemerle, Jean</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3788-e63037313c2a6bd83269954d66415ee129f49dfa944b03861c22ba63d02b6cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Age Factors</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Fibroma - pathology</topic><topic>fibrosarcoma</topic><topic>Fibrosarcoma - pathology</topic><topic>Hemangioma - pathology</topic><topic>hemangiopericytoma</topic><topic>Hemangiopericytoma - pathology</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Neoplasm Recurrence, Local</topic><topic>Sarcoma - pathology</topic><topic>Soft Tissue Neoplasms - diagnosis</topic><topic>Soft Tissue Neoplasms - pathology</topic><topic>Soft Tissue Neoplasms - therapy</topic><topic>unclassified sarcoma</topic><toplevel>online_resources</toplevel><creatorcontrib>Salloum, Emile</creatorcontrib><creatorcontrib>Flamant, Françoise</creatorcontrib><creatorcontrib>Caillaud, Jean M.</creatorcontrib><creatorcontrib>Friedman, Samuel</creatorcontrib><creatorcontrib>Wacker, Pierre</creatorcontrib><creatorcontrib>Coppes, Max J.</creatorcontrib><creatorcontrib>Brugieres, Laurence</creatorcontrib><creatorcontrib>Lemerle, Jean</creatorcontrib><collection>Istex</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>Salloum, Emile</au><au>Flamant, Françoise</au><au>Caillaud, Jean M.</au><au>Friedman, Samuel</au><au>Wacker, Pierre</au><au>Coppes, Max J.</au><au>Brugieres, Laurence</au><au>Lemerle, Jean</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnostic and therapeutic problems of soft tissue tumors other than rhabdomyosarcoma in infants under 1 year of age: A clinicopathological study of 34 cases treated at the institut gustave-roussy</atitle><jtitle>Medical and pediatric oncology</jtitle><addtitle>Med. Pediatr. Oncol</addtitle><date>1990</date><risdate>1990</risdate><volume>18</volume><issue>1</issue><spage>37</spage><epage>43</epage><pages>37-43</pages><issn>0098-1532</issn><eissn>1096-911X</eissn><abstract>Thirty‐four cases of soft tissue tumors (STT) other than rhabdomyosarcoma in infants under 1 year of age were seen in our institution between 1955 and 1985. All were diagnosed initially as malignant tumors except for three cases of fibromatosis, and, thus, they received therapy appropriate at that time. During a recent pathologic review, four were seen to have had hemangioma, six hemangiopericytoma, one hamartoma, seven fibromatosis, eight fibrosarcoma, and eight unclassified sarcomas. Of these 34 cases, the initial histological diagnosis was confirmed in only 17. Sixteen patients were believed to have received inappropriately aggressive therapy; indeed, four of these cases diagnosed prior to 1975 had been benign. Major long‐term side effects were seen in 7/16 treated patients (six radiotherapy, one surgery), who, in retrospect, should have received less aggressive treatment.
The reasons for these initial errors in diagnosis included doubtful histologic features associated in some cases with alarming clinical presentation. We believe that difficulties still remain in distinguishing benign from malignant STT in this age group by histological examination. Therefore, we urge extreme caution in using aggressive therapy before the diagnosis is certain.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2294390</pmid><doi>10.1002/mpo.2950180108</doi><tpages>7</tpages></addata></record> |
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subjects | Age Factors Diagnosis, Differential Female Fibroma - pathology fibrosarcoma Fibrosarcoma - pathology Hemangioma - pathology hemangiopericytoma Hemangiopericytoma - pathology Humans Infant Infant, Newborn Male Neoplasm Recurrence, Local Sarcoma - pathology Soft Tissue Neoplasms - diagnosis Soft Tissue Neoplasms - pathology Soft Tissue Neoplasms - therapy unclassified sarcoma |
title | Diagnostic and therapeutic problems of soft tissue tumors other than rhabdomyosarcoma in infants under 1 year of age: A clinicopathological study of 34 cases treated at the institut gustave-roussy |
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