Loading…

Simultaneous sex cord stromal tumor with annular tubules, adenocarcinoma of the cervix and intraductal papilloma of the breast in a patient with Peutz–Jeghers syndrome: a case report

Peutz–Jeghers syndrome was first described by a Dutch physician, Jan Peutz, in 1921. It is an inherited syndrome characterized by intestinal hamartomatous polyps, which can cause obstruction, and mucocutaneous hyperpigmentation. This rare syndrome brings a 15-fold increase in the risk of intestinal...

Full description

Saved in:
Bibliographic Details
Published in:Current Gynecologic Oncology 2015-11, Vol.13 (3), p.180-184
Main Authors: Takmaz, Ozguc, Iyibozkurt, Cem
Format: Article
Language:eng ; pol
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c1126-c3cfe7de20bab9a2cd3c2401f1a554a8adabc1a07246d5ca29870e36472c05413
cites
container_end_page 184
container_issue 3
container_start_page 180
container_title Current Gynecologic Oncology
container_volume 13
creator Takmaz, Ozguc
Iyibozkurt, Cem
description Peutz–Jeghers syndrome was first described by a Dutch physician, Jan Peutz, in 1921. It is an inherited syndrome characterized by intestinal hamartomatous polyps, which can cause obstruction, and mucocutaneous hyperpigmentation. This rare syndrome brings a 15-fold increase in the risk of intestinal as well as gynecologic tumors, especially ovarian cancer. We present a 49-year-old women with a huge adnexal mass and already diagnosed Peutz–Jeghers syndrome. Although the sampling of the endometrium, which was done before the surgery, was normal, cervical adenocarcinoma (adenoma malignum) was diagnosed after the operation, and complementary radical trachelectomy was conducted to complete the therapy. In conclusion, Peutz–Jeghers syndrome patients are at an increased risk of genital tract tumors. It should be kept in mind that a clinical examination could be insufficient to diagnose all the tumoral components of the disease.
doi_str_mv 10.15557/CGO.2015.0020
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2708644626</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2708644626</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1126-c3cfe7de20bab9a2cd3c2401f1a554a8adabc1a07246d5ca29870e36472c05413</originalsourceid><addsrcrecordid>eNpNkc9KxDAQxosoKOrVc8CruyZp2u56k0VXRVBQz2WaTN1KN6mTxH8n38GX8Xl8EqPrwdMMMz--74Mvy_YEH4uiKKrD2fxqLLkoxpxLvpZtST4RI1Hmcv3fvpntev_AEzItlazUVvZ50y1jH8Cii555fGHakWE-kFtCz0JcOmLPXVgwsDb2QOnUxB79AQOD1mkg3dnEMteysECmkZ66l0Qb1tlAYKIOSWiAoev7f1xDCD4khkF6hg5tWPlcYwxvX-8fF3i_QEqZXq1JYfAogRo8MsLBUdjJNlroPe7-ze3s7vTkdnY2uryan8-OL0daCFmOdK5brAxK3kAzBalNrqXiohVQFAomYKDRAnglVWkKDXI6qTjmpaqk5oUS-Xa2v9IdyD1G9KF-cJFssqxlxSelUqUsEzVeUZqc94RtPVC3BHqtBa9_C6pTQfVPQfVPQfk324SIMA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2708644626</pqid></control><display><type>article</type><title>Simultaneous sex cord stromal tumor with annular tubules, adenocarcinoma of the cervix and intraductal papilloma of the breast in a patient with Peutz–Jeghers syndrome: a case report</title><source>Publicly Available Content (ProQuest)</source><creator>Takmaz, Ozguc ; Iyibozkurt, Cem</creator><creatorcontrib>Takmaz, Ozguc ; Iyibozkurt, Cem ; Department of Gynecologic Oncology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey ; Department of Gynecology and Obstetrics, Acibadem Maslak Hospital, Istanbul, Turkey</creatorcontrib><description>Peutz–Jeghers syndrome was first described by a Dutch physician, Jan Peutz, in 1921. It is an inherited syndrome characterized by intestinal hamartomatous polyps, which can cause obstruction, and mucocutaneous hyperpigmentation. This rare syndrome brings a 15-fold increase in the risk of intestinal as well as gynecologic tumors, especially ovarian cancer. We present a 49-year-old women with a huge adnexal mass and already diagnosed Peutz–Jeghers syndrome. Although the sampling of the endometrium, which was done before the surgery, was normal, cervical adenocarcinoma (adenoma malignum) was diagnosed after the operation, and complementary radical trachelectomy was conducted to complete the therapy. In conclusion, Peutz–Jeghers syndrome patients are at an increased risk of genital tract tumors. It should be kept in mind that a clinical examination could be insufficient to diagnose all the tumoral components of the disease.</description><identifier>ISSN: 2081-1632</identifier><identifier>EISSN: 2081-1632</identifier><identifier>DOI: 10.15557/CGO.2015.0020</identifier><language>eng ; pol</language><publisher>Warsaw: Medical Communications Sp. z o.o</publisher><subject>Case reports ; Cervical cancer ; Ovarian cancer ; Tumors</subject><ispartof>Current Gynecologic Oncology, 2015-11, Vol.13 (3), p.180-184</ispartof><rights>2015. This work is published under http://creativecommons.org/licenses/by-nc-nd/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><citedby>FETCH-LOGICAL-c1126-c3cfe7de20bab9a2cd3c2401f1a554a8adabc1a07246d5ca29870e36472c05413</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2708644626?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590</link.rule.ids></links><search><creatorcontrib>Takmaz, Ozguc</creatorcontrib><creatorcontrib>Iyibozkurt, Cem</creatorcontrib><creatorcontrib>Department of Gynecologic Oncology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey</creatorcontrib><creatorcontrib>Department of Gynecology and Obstetrics, Acibadem Maslak Hospital, Istanbul, Turkey</creatorcontrib><title>Simultaneous sex cord stromal tumor with annular tubules, adenocarcinoma of the cervix and intraductal papilloma of the breast in a patient with Peutz–Jeghers syndrome: a case report</title><title>Current Gynecologic Oncology</title><description>Peutz–Jeghers syndrome was first described by a Dutch physician, Jan Peutz, in 1921. It is an inherited syndrome characterized by intestinal hamartomatous polyps, which can cause obstruction, and mucocutaneous hyperpigmentation. This rare syndrome brings a 15-fold increase in the risk of intestinal as well as gynecologic tumors, especially ovarian cancer. We present a 49-year-old women with a huge adnexal mass and already diagnosed Peutz–Jeghers syndrome. Although the sampling of the endometrium, which was done before the surgery, was normal, cervical adenocarcinoma (adenoma malignum) was diagnosed after the operation, and complementary radical trachelectomy was conducted to complete the therapy. In conclusion, Peutz–Jeghers syndrome patients are at an increased risk of genital tract tumors. It should be kept in mind that a clinical examination could be insufficient to diagnose all the tumoral components of the disease.</description><subject>Case reports</subject><subject>Cervical cancer</subject><subject>Ovarian cancer</subject><subject>Tumors</subject><issn>2081-1632</issn><issn>2081-1632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpNkc9KxDAQxosoKOrVc8CruyZp2u56k0VXRVBQz2WaTN1KN6mTxH8n38GX8Xl8EqPrwdMMMz--74Mvy_YEH4uiKKrD2fxqLLkoxpxLvpZtST4RI1Hmcv3fvpntev_AEzItlazUVvZ50y1jH8Cii555fGHakWE-kFtCz0JcOmLPXVgwsDb2QOnUxB79AQOD1mkg3dnEMteysECmkZ66l0Qb1tlAYKIOSWiAoev7f1xDCD4khkF6hg5tWPlcYwxvX-8fF3i_QEqZXq1JYfAogRo8MsLBUdjJNlroPe7-ze3s7vTkdnY2uryan8-OL0daCFmOdK5brAxK3kAzBalNrqXiohVQFAomYKDRAnglVWkKDXI6qTjmpaqk5oUS-Xa2v9IdyD1G9KF-cJFssqxlxSelUqUsEzVeUZqc94RtPVC3BHqtBa9_C6pTQfVPQfVPQfk324SIMA</recordid><startdate>20151130</startdate><enddate>20151130</enddate><creator>Takmaz, Ozguc</creator><creator>Iyibozkurt, Cem</creator><general>Medical Communications Sp. z o.o</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</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>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20151130</creationdate><title>Simultaneous sex cord stromal tumor with annular tubules, adenocarcinoma of the cervix and intraductal papilloma of the breast in a patient with Peutz–Jeghers syndrome: a case report</title><author>Takmaz, Ozguc ; Iyibozkurt, Cem</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1126-c3cfe7de20bab9a2cd3c2401f1a554a8adabc1a07246d5ca29870e36472c05413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; pol</language><creationdate>2015</creationdate><topic>Case reports</topic><topic>Cervical cancer</topic><topic>Ovarian cancer</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takmaz, Ozguc</creatorcontrib><creatorcontrib>Iyibozkurt, Cem</creatorcontrib><creatorcontrib>Department of Gynecologic Oncology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey</creatorcontrib><creatorcontrib>Department of Gynecology and Obstetrics, Acibadem Maslak Hospital, Istanbul, Turkey</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection (ProQuest Medical &amp; Health Databases)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content (ProQuest)</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>Current Gynecologic Oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takmaz, Ozguc</au><au>Iyibozkurt, Cem</au><aucorp>Department of Gynecologic Oncology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey</aucorp><aucorp>Department of Gynecology and Obstetrics, Acibadem Maslak Hospital, Istanbul, Turkey</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous sex cord stromal tumor with annular tubules, adenocarcinoma of the cervix and intraductal papilloma of the breast in a patient with Peutz–Jeghers syndrome: a case report</atitle><jtitle>Current Gynecologic Oncology</jtitle><date>2015-11-30</date><risdate>2015</risdate><volume>13</volume><issue>3</issue><spage>180</spage><epage>184</epage><pages>180-184</pages><issn>2081-1632</issn><eissn>2081-1632</eissn><abstract>Peutz–Jeghers syndrome was first described by a Dutch physician, Jan Peutz, in 1921. It is an inherited syndrome characterized by intestinal hamartomatous polyps, which can cause obstruction, and mucocutaneous hyperpigmentation. This rare syndrome brings a 15-fold increase in the risk of intestinal as well as gynecologic tumors, especially ovarian cancer. We present a 49-year-old women with a huge adnexal mass and already diagnosed Peutz–Jeghers syndrome. Although the sampling of the endometrium, which was done before the surgery, was normal, cervical adenocarcinoma (adenoma malignum) was diagnosed after the operation, and complementary radical trachelectomy was conducted to complete the therapy. In conclusion, Peutz–Jeghers syndrome patients are at an increased risk of genital tract tumors. It should be kept in mind that a clinical examination could be insufficient to diagnose all the tumoral components of the disease.</abstract><cop>Warsaw</cop><pub>Medical Communications Sp. z o.o</pub><doi>10.15557/CGO.2015.0020</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2081-1632
ispartof Current Gynecologic Oncology, 2015-11, Vol.13 (3), p.180-184
issn 2081-1632
2081-1632
language eng ; pol
recordid cdi_proquest_journals_2708644626
source Publicly Available Content (ProQuest)
subjects Case reports
Cervical cancer
Ovarian cancer
Tumors
title Simultaneous sex cord stromal tumor with annular tubules, adenocarcinoma of the cervix and intraductal papilloma of the breast in a patient with Peutz–Jeghers syndrome: a case report
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T12%3A26%3A27IST&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=Simultaneous%20sex%20cord%20stromal%20tumor%20with%20annular%20tubules,%20adenocarcinoma%20of%20the%20cervix%20and%20intraductal%20papilloma%20of%20the%20breast%20in%20a%20patient%20with%20Peutz%E2%80%93Jeghers%20syndrome:%20a%20case%20report&rft.jtitle=Current%20Gynecologic%20Oncology&rft.au=Takmaz,%20Ozguc&rft.aucorp=Department%20of%20Gynecologic%20Oncology,%20Istanbul%20Faculty%20of%20Medicine,%20Istanbul%20University,%20Istanbul,%20Turkey&rft.date=2015-11-30&rft.volume=13&rft.issue=3&rft.spage=180&rft.epage=184&rft.pages=180-184&rft.issn=2081-1632&rft.eissn=2081-1632&rft_id=info:doi/10.15557/CGO.2015.0020&rft_dat=%3Cproquest_cross%3E2708644626%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c1126-c3cfe7de20bab9a2cd3c2401f1a554a8adabc1a07246d5ca29870e36472c05413%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2708644626&rft_id=info:pmid/&rfr_iscdi=true