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Retroperitoneal myofibroblastoma in an 88‐year‐old male
Introduction Extramammary myofibroblastomas are extremely rare. Case presentation The patient was an 88‐year‐old male. He presented for evaluation of frequent urination and a “pushing up” sensation from the groin during defecation. Thorough physical and radiographic examinations revealed a retroperi...
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Published in: | IJU case reports 2022-09, Vol.5 (5), p.378-382 |
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description | Introduction
Extramammary myofibroblastomas are extremely rare.
Case presentation
The patient was an 88‐year‐old male. He presented for evaluation of frequent urination and a “pushing up” sensation from the groin during defecation. Thorough physical and radiographic examinations revealed a retroperitoneal tumor on the right side of the rectum. The pathologic examination of the biopsy tissue showed that the tumor was unlikely to be malignant. Nevertheless, the patient was symptomatic and thus underwent a laparoscopic tumor resection through a transperitoneal approach. The tumor was circumscribed with a solid capsule. Based on the pathologic findings, which included immunostaining, the tumor was diagnosed as a myofibroblastoma. There was no evidence of a recurrence 6 months postoperatively.
Conclusion
We present this case with the clinical course and surgical findings, and discuss the possibility of establishing a preoperative pathologic diagnosis of a myofibroblastoma. |
doi_str_mv | 10.1002/iju5.12493 |
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Extramammary myofibroblastomas are extremely rare.
Case presentation
The patient was an 88‐year‐old male. He presented for evaluation of frequent urination and a “pushing up” sensation from the groin during defecation. Thorough physical and radiographic examinations revealed a retroperitoneal tumor on the right side of the rectum. The pathologic examination of the biopsy tissue showed that the tumor was unlikely to be malignant. Nevertheless, the patient was symptomatic and thus underwent a laparoscopic tumor resection through a transperitoneal approach. The tumor was circumscribed with a solid capsule. Based on the pathologic findings, which included immunostaining, the tumor was diagnosed as a myofibroblastoma. There was no evidence of a recurrence 6 months postoperatively.
Conclusion
We present this case with the clinical course and surgical findings, and discuss the possibility of establishing a preoperative pathologic diagnosis of a myofibroblastoma.</description><identifier>ISSN: 2577-171X</identifier><identifier>EISSN: 2577-171X</identifier><identifier>DOI: 10.1002/iju5.12493</identifier><identifier>PMID: 36090948</identifier><language>eng</language><publisher>Tokyo: John Wiley & Sons, Inc</publisher><subject>Abdomen ; Biopsy ; Case Report ; Case Reports ; Estrogens ; Gastric cancer ; Laparoscopy ; Magnetic resonance imaging ; myofibroblastoma ; pathology ; retroperitoneal neoplasms ; Surgery ; surgical procedure ; Tumors ; Writing</subject><ispartof>IJU case reports, 2022-09, Vol.5 (5), p.378-382</ispartof><rights>2022 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Urological Association.</rights><rights>2022. 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-c5103-f0d65e07ab723eeefefec69f290175e732ef9a41212bda425a94bddcfd68c4493</citedby><cites>FETCH-LOGICAL-c5103-f0d65e07ab723eeefefec69f290175e732ef9a41212bda425a94bddcfd68c4493</cites><orcidid>0000-0002-3485-2565 ; 0000-0001-6352-8089</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2708825720/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2708825720?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,44590,46052,46476,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>Watari, Shogo</creatorcontrib><creatorcontrib>Ichikawa, Takaharu</creatorcontrib><creatorcontrib>Shiraishi, Hiromasa</creatorcontrib><creatorcontrib>Sakuma, Takafumi</creatorcontrib><creatorcontrib>Kubota, Risa</creatorcontrib><creatorcontrib>Kusumi, Norihiro</creatorcontrib><creatorcontrib>Tsushima, Tomoyasu</creatorcontrib><creatorcontrib>Nagakita, Keina</creatorcontrib><creatorcontrib>Shinno, Yoko</creatorcontrib><title>Retroperitoneal myofibroblastoma in an 88‐year‐old male</title><title>IJU case reports</title><description>Introduction
Extramammary myofibroblastomas are extremely rare.
Case presentation
The patient was an 88‐year‐old male. He presented for evaluation of frequent urination and a “pushing up” sensation from the groin during defecation. Thorough physical and radiographic examinations revealed a retroperitoneal tumor on the right side of the rectum. The pathologic examination of the biopsy tissue showed that the tumor was unlikely to be malignant. Nevertheless, the patient was symptomatic and thus underwent a laparoscopic tumor resection through a transperitoneal approach. The tumor was circumscribed with a solid capsule. Based on the pathologic findings, which included immunostaining, the tumor was diagnosed as a myofibroblastoma. There was no evidence of a recurrence 6 months postoperatively.
Conclusion
We present this case with the clinical course and surgical findings, and discuss the possibility of establishing a preoperative pathologic diagnosis of a myofibroblastoma.</description><subject>Abdomen</subject><subject>Biopsy</subject><subject>Case Report</subject><subject>Case Reports</subject><subject>Estrogens</subject><subject>Gastric cancer</subject><subject>Laparoscopy</subject><subject>Magnetic resonance imaging</subject><subject>myofibroblastoma</subject><subject>pathology</subject><subject>retroperitoneal neoplasms</subject><subject>Surgery</subject><subject>surgical procedure</subject><subject>Tumors</subject><subject>Writing</subject><issn>2577-171X</issn><issn>2577-171X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kd9qFDEUh4MotrS98QkGvBO2Jmcy-YMgSLF1pVAQC96FM8lJnWVmsmZmLXvnI_iMfRLTThF7I4GckHz5wsmPsVeCnwrO4W232TWnAqStn7FDaLReCS2-Pf9nfcBOpmnDC8xFrSS8ZAe14pZbaQ7Zuy8057Sl3M1pJOyrYZ9i1-bU9jjNacCqGyscK2Pufv3eE-ZSUh-qAXs6Zi8i9hOdPNYjdn3-8evZp9Xl1cX67MPlyjeC16vIg2qIa2w11EQUy_DKRrBc6IZ0DRQtSgEC2oASGrSyDcHHoIyXpbEjtl68IeHGbXM3YN67hJ172Ej5xmGeO9-Ti9baqBAUeSMBAH2ZAmkEE6AFKq73i2u7awcKnsY5Y_9E-vRk7L67m_TTWVkrZWQRvH4U5PRjR9PsNmmXx9K_A82NKd8OvFBvFsrnNE2Z4t8XBHf3ubn73NxDbgUWC3zb9bT_D-nWn6-b5c4f61ubKg</recordid><startdate>202209</startdate><enddate>202209</enddate><creator>Watari, Shogo</creator><creator>Ichikawa, Takaharu</creator><creator>Shiraishi, Hiromasa</creator><creator>Sakuma, Takafumi</creator><creator>Kubota, Risa</creator><creator>Kusumi, Norihiro</creator><creator>Tsushima, Tomoyasu</creator><creator>Nagakita, Keina</creator><creator>Shinno, Yoko</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</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>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3485-2565</orcidid><orcidid>https://orcid.org/0000-0001-6352-8089</orcidid></search><sort><creationdate>202209</creationdate><title>Retroperitoneal myofibroblastoma in an 88‐year‐old male</title><author>Watari, Shogo ; Ichikawa, Takaharu ; Shiraishi, Hiromasa ; Sakuma, Takafumi ; Kubota, Risa ; Kusumi, Norihiro ; Tsushima, Tomoyasu ; Nagakita, Keina ; Shinno, Yoko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5103-f0d65e07ab723eeefefec69f290175e732ef9a41212bda425a94bddcfd68c4493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Abdomen</topic><topic>Biopsy</topic><topic>Case Report</topic><topic>Case Reports</topic><topic>Estrogens</topic><topic>Gastric cancer</topic><topic>Laparoscopy</topic><topic>Magnetic resonance imaging</topic><topic>myofibroblastoma</topic><topic>pathology</topic><topic>retroperitoneal neoplasms</topic><topic>Surgery</topic><topic>surgical procedure</topic><topic>Tumors</topic><topic>Writing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Watari, Shogo</creatorcontrib><creatorcontrib>Ichikawa, Takaharu</creatorcontrib><creatorcontrib>Shiraishi, Hiromasa</creatorcontrib><creatorcontrib>Sakuma, Takafumi</creatorcontrib><creatorcontrib>Kubota, Risa</creatorcontrib><creatorcontrib>Kusumi, Norihiro</creatorcontrib><creatorcontrib>Tsushima, Tomoyasu</creatorcontrib><creatorcontrib>Nagakita, Keina</creatorcontrib><creatorcontrib>Shinno, Yoko</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Free Content</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>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 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 Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</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><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>IJU case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Watari, Shogo</au><au>Ichikawa, Takaharu</au><au>Shiraishi, Hiromasa</au><au>Sakuma, Takafumi</au><au>Kubota, Risa</au><au>Kusumi, Norihiro</au><au>Tsushima, Tomoyasu</au><au>Nagakita, Keina</au><au>Shinno, Yoko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retroperitoneal myofibroblastoma in an 88‐year‐old male</atitle><jtitle>IJU case reports</jtitle><date>2022-09</date><risdate>2022</risdate><volume>5</volume><issue>5</issue><spage>378</spage><epage>382</epage><pages>378-382</pages><issn>2577-171X</issn><eissn>2577-171X</eissn><abstract>Introduction
Extramammary myofibroblastomas are extremely rare.
Case presentation
The patient was an 88‐year‐old male. He presented for evaluation of frequent urination and a “pushing up” sensation from the groin during defecation. Thorough physical and radiographic examinations revealed a retroperitoneal tumor on the right side of the rectum. The pathologic examination of the biopsy tissue showed that the tumor was unlikely to be malignant. Nevertheless, the patient was symptomatic and thus underwent a laparoscopic tumor resection through a transperitoneal approach. The tumor was circumscribed with a solid capsule. Based on the pathologic findings, which included immunostaining, the tumor was diagnosed as a myofibroblastoma. There was no evidence of a recurrence 6 months postoperatively.
Conclusion
We present this case with the clinical course and surgical findings, and discuss the possibility of establishing a preoperative pathologic diagnosis of a myofibroblastoma.</abstract><cop>Tokyo</cop><pub>John Wiley & Sons, Inc</pub><pmid>36090948</pmid><doi>10.1002/iju5.12493</doi><tpages>383</tpages><orcidid>https://orcid.org/0000-0002-3485-2565</orcidid><orcidid>https://orcid.org/0000-0001-6352-8089</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Biopsy Case Report Case Reports Estrogens Gastric cancer Laparoscopy Magnetic resonance imaging myofibroblastoma pathology retroperitoneal neoplasms Surgery surgical procedure Tumors Writing |
title | Retroperitoneal myofibroblastoma in an 88‐year‐old male |
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