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Rectocolic familial polyposis; a study of 32 cases
Thirty‐two cases of diffuse rectocolic polyposis, with a more or less marked hereditary character, have been analyzed. The homogeneity of the series, derived from the same surgical source and with the cooperation of a genetics department for the familial survey and detection, allowed precise observa...
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Published in: | World journal of surgery 1981-07, Vol.5 (4), p.617-625 |
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creator | Bigay, D. Plauchu, H. Berard, Ph Robert, J. M. Guillemin, G. |
description | Thirty‐two cases of diffuse rectocolic polyposis, with a more or less marked hereditary character, have been analyzed. The homogeneity of the series, derived from the same surgical source and with the cooperation of a genetics department for the familial survey and detection, allowed precise observations on the evolution and treatment of the disease. Besides the imperative indications for removal of the rectum in those cases determined by endoscopy to be either locally degenerate or uncontrollable, a surgical protocol designed to meet more precisely the diagnostic needs must be developed, based on the preservation of the rectum and resulting in its unlimited supervision.
Résumé
Analyse de 32 cas de polypose rectocolique, dont le caractère hériditaire est plus ou moins marqué. Des observations précises sur l'évolution et le traitement de la maladie ont été possibles, grâce à l'homogénéité du groupe de malades tous suivis dans le mÊme centre chirurgical et grâce à la coopération du départment de génétique pour la surveillance familiale et la détection des cas.
L'amputation de rectum est obligatoire dans les cas de cancérisation locale et dans les formes non controlables par l'endoscopie. Mais, dans un programme de détection précoce, il faut prévoir un protocole thérapeutique chirurgical qui conserve le rectum et assure sa surveillance pendant la vie entière du malade. |
doi_str_mv | 10.1007/BF01655018 |
format | article |
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Résumé
Analyse de 32 cas de polypose rectocolique, dont le caractère hériditaire est plus ou moins marqué. Des observations précises sur l'évolution et le traitement de la maladie ont été possibles, grâce à l'homogénéité du groupe de malades tous suivis dans le mÊme centre chirurgical et grâce à la coopération du départment de génétique pour la surveillance familiale et la détection des cas.
L'amputation de rectum est obligatoire dans les cas de cancérisation locale et dans les formes non controlables par l'endoscopie. Mais, dans un programme de détection précoce, il faut prévoir un protocole thérapeutique chirurgical qui conserve le rectum et assure sa surveillance pendant la vie entière du malade.</description><identifier>ISSN: 0364-2313</identifier><identifier>EISSN: 1432-2323</identifier><identifier>DOI: 10.1007/BF01655018</identifier><identifier>PMID: 7324496</identifier><language>eng</language><publisher>New York: Springer‐Verlag</publisher><subject>Adolescent ; Adult ; Assure ; Colectomy ; Colonic Neoplasms - genetics ; Colonic Neoplasms - surgery ; Familial Polyposis ; Female ; Follow-Up Studies ; Genetic Department ; Humans ; Intestinal Polyps - genetics ; Intestinal Polyps - surgery ; Male ; Middle Aged ; Precise Observation ; Public Health ; Rectal Neoplasms - genetics ; Rectal Neoplasms - surgery ; Rectum - surgery</subject><ispartof>World journal of surgery, 1981-07, Vol.5 (4), p.617-625</ispartof><rights>1981 International Society of Surgery</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2438-c4262eaa38bc3a79ea9f0f9a30d1d0880fe5cdba079c532f2f3ade9269e336d83</citedby><cites>FETCH-LOGICAL-c2438-c4262eaa38bc3a79ea9f0f9a30d1d0880fe5cdba079c532f2f3ade9269e336d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7324496$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bigay, D.</creatorcontrib><creatorcontrib>Plauchu, H.</creatorcontrib><creatorcontrib>Berard, Ph</creatorcontrib><creatorcontrib>Robert, J. M.</creatorcontrib><creatorcontrib>Guillemin, G.</creatorcontrib><title>Rectocolic familial polyposis; a study of 32 cases</title><title>World journal of surgery</title><addtitle>World J Surg</addtitle><description>Thirty‐two cases of diffuse rectocolic polyposis, with a more or less marked hereditary character, have been analyzed. The homogeneity of the series, derived from the same surgical source and with the cooperation of a genetics department for the familial survey and detection, allowed precise observations on the evolution and treatment of the disease. Besides the imperative indications for removal of the rectum in those cases determined by endoscopy to be either locally degenerate or uncontrollable, a surgical protocol designed to meet more precisely the diagnostic needs must be developed, based on the preservation of the rectum and resulting in its unlimited supervision.
Résumé
Analyse de 32 cas de polypose rectocolique, dont le caractère hériditaire est plus ou moins marqué. Des observations précises sur l'évolution et le traitement de la maladie ont été possibles, grâce à l'homogénéité du groupe de malades tous suivis dans le mÊme centre chirurgical et grâce à la coopération du départment de génétique pour la surveillance familiale et la détection des cas.
L'amputation de rectum est obligatoire dans les cas de cancérisation locale et dans les formes non controlables par l'endoscopie. Mais, dans un programme de détection précoce, il faut prévoir un protocole thérapeutique chirurgical qui conserve le rectum et assure sa surveillance pendant la vie entière du malade.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Assure</subject><subject>Colectomy</subject><subject>Colonic Neoplasms - genetics</subject><subject>Colonic Neoplasms - surgery</subject><subject>Familial Polyposis</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Genetic Department</subject><subject>Humans</subject><subject>Intestinal Polyps - genetics</subject><subject>Intestinal Polyps - surgery</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Precise Observation</subject><subject>Public Health</subject><subject>Rectal Neoplasms - genetics</subject><subject>Rectal Neoplasms - surgery</subject><subject>Rectum - surgery</subject><issn>0364-2313</issn><issn>1432-2323</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNp9kM1LxDAQR4Mo67p68S705EGoTjJpmuJJF9cPFgQ_8Fhm0wQqqanNFul_7y67qCdPM_B7vMNj7JjDOQfIL65nwFWWAdc7bMwlilSgwF02BlRy9XPcZwcxvgPwXIEasVGOQspCjZl4smYZTPC1SRw1ta_JJ23wQxtiHS8TSuKyr4YkuARFYijaeMj2HPloj7Z3wl5nNy_Tu3T-eHs_vZqnRkjUqZFCCUuEemGQ8sJS4cAVhFDxCrQGZzNTLQjywmQonHBIlS2EKiyiqjRO2OnG23bhs7dxWTZ1NNZ7-rChj2WOmisJa_BsA5ouxNhZV7Zd3VA3lBzKdaDyN9AKPtla-0Vjqx90W2S1Z5v9q_Z2-MdUvj08__F-A56Rbd8</recordid><startdate>198107</startdate><enddate>198107</enddate><creator>Bigay, D.</creator><creator>Plauchu, H.</creator><creator>Berard, Ph</creator><creator>Robert, J. M.</creator><creator>Guillemin, G.</creator><general>Springer‐Verlag</general><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>198107</creationdate><title>Rectocolic familial polyposis; a study of 32 cases</title><author>Bigay, D. ; Plauchu, H. ; Berard, Ph ; Robert, J. M. ; Guillemin, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2438-c4262eaa38bc3a79ea9f0f9a30d1d0880fe5cdba079c532f2f3ade9269e336d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Assure</topic><topic>Colectomy</topic><topic>Colonic Neoplasms - genetics</topic><topic>Colonic Neoplasms - surgery</topic><topic>Familial Polyposis</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Genetic Department</topic><topic>Humans</topic><topic>Intestinal Polyps - genetics</topic><topic>Intestinal Polyps - surgery</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Precise Observation</topic><topic>Public Health</topic><topic>Rectal Neoplasms - genetics</topic><topic>Rectal Neoplasms - surgery</topic><topic>Rectum - surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bigay, D.</creatorcontrib><creatorcontrib>Plauchu, H.</creatorcontrib><creatorcontrib>Berard, Ph</creatorcontrib><creatorcontrib>Robert, J. M.</creatorcontrib><creatorcontrib>Guillemin, G.</creatorcontrib><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>World journal of surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bigay, D.</au><au>Plauchu, H.</au><au>Berard, Ph</au><au>Robert, J. M.</au><au>Guillemin, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rectocolic familial polyposis; a study of 32 cases</atitle><jtitle>World journal of surgery</jtitle><addtitle>World J Surg</addtitle><date>1981-07</date><risdate>1981</risdate><volume>5</volume><issue>4</issue><spage>617</spage><epage>625</epage><pages>617-625</pages><issn>0364-2313</issn><eissn>1432-2323</eissn><abstract>Thirty‐two cases of diffuse rectocolic polyposis, with a more or less marked hereditary character, have been analyzed. The homogeneity of the series, derived from the same surgical source and with the cooperation of a genetics department for the familial survey and detection, allowed precise observations on the evolution and treatment of the disease. Besides the imperative indications for removal of the rectum in those cases determined by endoscopy to be either locally degenerate or uncontrollable, a surgical protocol designed to meet more precisely the diagnostic needs must be developed, based on the preservation of the rectum and resulting in its unlimited supervision.
Résumé
Analyse de 32 cas de polypose rectocolique, dont le caractère hériditaire est plus ou moins marqué. Des observations précises sur l'évolution et le traitement de la maladie ont été possibles, grâce à l'homogénéité du groupe de malades tous suivis dans le mÊme centre chirurgical et grâce à la coopération du départment de génétique pour la surveillance familiale et la détection des cas.
L'amputation de rectum est obligatoire dans les cas de cancérisation locale et dans les formes non controlables par l'endoscopie. Mais, dans un programme de détection précoce, il faut prévoir un protocole thérapeutique chirurgical qui conserve le rectum et assure sa surveillance pendant la vie entière du malade.</abstract><cop>New York</cop><pub>Springer‐Verlag</pub><pmid>7324496</pmid><doi>10.1007/BF01655018</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Assure Colectomy Colonic Neoplasms - genetics Colonic Neoplasms - surgery Familial Polyposis Female Follow-Up Studies Genetic Department Humans Intestinal Polyps - genetics Intestinal Polyps - surgery Male Middle Aged Precise Observation Public Health Rectal Neoplasms - genetics Rectal Neoplasms - surgery Rectum - surgery |
title | Rectocolic familial polyposis; a study of 32 cases |
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