The ectopic vesical pheochromocytoma a diagnostic and therapeutic challenge case report and literature review
•Pheochromocytoma is a tumor developed at the expense of chromaffin tissues.•Extra-adrenal localization of pheochromocytoma is rare.•The main problem with these tumors is to affirm their benignity or malignancy.•Ectopic pheochromocytomas have a malignant development once in two.•Ectopic pheochromocy...
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creator | Jandou, Issam Moataz, Amine Mouqtassid, Mohammed Hicham Dakir, Mohammed Debbagh, Adil Aboutaieb, Rachid |
description | •Pheochromocytoma is a tumor developed at the expense of chromaffin tissues.•Extra-adrenal localization of pheochromocytoma is rare.•The main problem with these tumors is to affirm their benignity or malignancy.•Ectopic pheochromocytomas have a malignant development once in two.•Ectopic pheochromocytoma presents a diagnostic and therapeutic dilemma.
Extra-adrenal localization of pheochromocytoma is rare. Its clinical revelation is paroxysmal but maybe in the form of permanent hypertension resistant to treatment. The main problem with these tumors is to affirm their benignity or malignancy, ectopic pheochromocytomas have a malignant development once in two.
We report the observation of a 39-year-old woman hypertensive on Amlodipine. She presents for sweating, headache, and palpation. The dosage of urinary metabolites revealed a marked increase in metanephrine and normetanephrine. Imagery had shown, at the expense of the left lateral wall of the bladder, a budding tissue formation with irregular contours which was significantly enhanced after injection of PDC. The diagnosis of an ectopic pheochromocytoma was accepted. The patient underwent a partial cystectomy, the postoperative consequences of which were unremarkable.
Threatening secretory syndromes are rare medical situations that require urgent management. Pheochromocytoma can be seen at any age from childhood to old age. The treatment of pheochromocytoma is surgical, once the stages of positive and topographic diagnosis have been carried out, the patient must be immediately entrusted to a team of trained surgeons and anesthetists. The prognosis remains unpredictable, hence the interest in prolonged monitoring.
Pheochromocytoma is a tumor developed at the expense of chromaffin tissues, extra-adrenal localizations exist, but remain rare. It is a pathology that presents a diagnostic and therapeutic dilemma in which patients require regular and prolonged postoperative monitoring to detect a possible metastasis or recurrence. |
doi_str_mv | 10.1016/j.ijscr.2020.11.132 |
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Extra-adrenal localization of pheochromocytoma is rare. Its clinical revelation is paroxysmal but maybe in the form of permanent hypertension resistant to treatment. The main problem with these tumors is to affirm their benignity or malignancy, ectopic pheochromocytomas have a malignant development once in two.
We report the observation of a 39-year-old woman hypertensive on Amlodipine. She presents for sweating, headache, and palpation. The dosage of urinary metabolites revealed a marked increase in metanephrine and normetanephrine. Imagery had shown, at the expense of the left lateral wall of the bladder, a budding tissue formation with irregular contours which was significantly enhanced after injection of PDC. The diagnosis of an ectopic pheochromocytoma was accepted. The patient underwent a partial cystectomy, the postoperative consequences of which were unremarkable.
Threatening secretory syndromes are rare medical situations that require urgent management. Pheochromocytoma can be seen at any age from childhood to old age. The treatment of pheochromocytoma is surgical, once the stages of positive and topographic diagnosis have been carried out, the patient must be immediately entrusted to a team of trained surgeons and anesthetists. The prognosis remains unpredictable, hence the interest in prolonged monitoring.
Pheochromocytoma is a tumor developed at the expense of chromaffin tissues, extra-adrenal localizations exist, but remain rare. It is a pathology that presents a diagnostic and therapeutic dilemma in which patients require regular and prolonged postoperative monitoring to detect a possible metastasis or recurrence.</description><identifier>ISSN: 2210-2612</identifier><identifier>EISSN: 2210-2612</identifier><identifier>DOI: 10.1016/j.ijscr.2020.11.132</identifier><identifier>PMID: 33395912</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Bladder pheochromocytoma ; Case Report ; Ectopic pheochromocytoma ; Methoxylated derivative ; Partial cystectomy</subject><ispartof>International journal of surgery case reports, 2020-01, Vol.77, p.857-861</ispartof><rights>2020 The Author(s)</rights><rights>Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.</rights><rights>2020 The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-bbb4548b2bba8175b737c2d76ac00ac220aa1908c43daed36a6cd763fce052423</citedby><cites>FETCH-LOGICAL-c426t-bbb4548b2bba8175b737c2d76ac00ac220aa1908c43daed36a6cd763fce052423</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726245/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2210261220311615$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3537,27901,27902,53766,53768,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33395912$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jandou, Issam</creatorcontrib><creatorcontrib>Moataz, Amine</creatorcontrib><creatorcontrib>Mouqtassid, Mohammed Hicham</creatorcontrib><creatorcontrib>Dakir, Mohammed</creatorcontrib><creatorcontrib>Debbagh, Adil</creatorcontrib><creatorcontrib>Aboutaieb, Rachid</creatorcontrib><title>The ectopic vesical pheochromocytoma a diagnostic and therapeutic challenge case report and literature review</title><title>International journal of surgery case reports</title><addtitle>Int J Surg Case Rep</addtitle><description>•Pheochromocytoma is a tumor developed at the expense of chromaffin tissues.•Extra-adrenal localization of pheochromocytoma is rare.•The main problem with these tumors is to affirm their benignity or malignancy.•Ectopic pheochromocytomas have a malignant development once in two.•Ectopic pheochromocytoma presents a diagnostic and therapeutic dilemma.
Extra-adrenal localization of pheochromocytoma is rare. Its clinical revelation is paroxysmal but maybe in the form of permanent hypertension resistant to treatment. The main problem with these tumors is to affirm their benignity or malignancy, ectopic pheochromocytomas have a malignant development once in two.
We report the observation of a 39-year-old woman hypertensive on Amlodipine. She presents for sweating, headache, and palpation. The dosage of urinary metabolites revealed a marked increase in metanephrine and normetanephrine. Imagery had shown, at the expense of the left lateral wall of the bladder, a budding tissue formation with irregular contours which was significantly enhanced after injection of PDC. The diagnosis of an ectopic pheochromocytoma was accepted. The patient underwent a partial cystectomy, the postoperative consequences of which were unremarkable.
Threatening secretory syndromes are rare medical situations that require urgent management. Pheochromocytoma can be seen at any age from childhood to old age. The treatment of pheochromocytoma is surgical, once the stages of positive and topographic diagnosis have been carried out, the patient must be immediately entrusted to a team of trained surgeons and anesthetists. The prognosis remains unpredictable, hence the interest in prolonged monitoring.
Pheochromocytoma is a tumor developed at the expense of chromaffin tissues, extra-adrenal localizations exist, but remain rare. It is a pathology that presents a diagnostic and therapeutic dilemma in which patients require regular and prolonged postoperative monitoring to detect a possible metastasis or recurrence.</description><subject>Bladder pheochromocytoma</subject><subject>Case Report</subject><subject>Ectopic pheochromocytoma</subject><subject>Methoxylated derivative</subject><subject>Partial cystectomy</subject><issn>2210-2612</issn><issn>2210-2612</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9UdtqGzEQFaGlMa6_oBD2B-xIo73YDwkU0xsY8pI-i9nZsVdmd7VIsov_vnLcBPclehnNzDlnmDlCfFFyoaQq7_cLuw_kFyAhVdRCabgREwAl51Aq-HD1vxWzEPYyPQ3LEuCTuNVar4qVgonon1vOmKIbLWVHDpawy8aWHbXe9Y5O0fWYYdZY3A0uxITCocliyx5HPpxzarHreNhxRhg48zw6H19QnY0JFg_-XD1a_vNZfNxiF3j2L07F7-_fntc_55unH7_WXzdzyqGM87qu8yJf1lDXuFRVUVe6ImiqEklKJACJqFZySblukBtdYkmpq7fEsoAc9FQ8XnTHQ91zQzxEj50Zve3Rn4xDa_7vDLY1O3c0VQUl5EUS0BcB8i4Ez9s3rpLmbIDZmxcDzNkAo5RJBiTW3fXYN87ruRPg4QLgtHw6iDeBLA_EjfXJBNM4--6Av_EynA8</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Jandou, Issam</creator><creator>Moataz, Amine</creator><creator>Mouqtassid, Mohammed Hicham</creator><creator>Dakir, Mohammed</creator><creator>Debbagh, Adil</creator><creator>Aboutaieb, Rachid</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20200101</creationdate><title>The ectopic vesical pheochromocytoma a diagnostic and therapeutic challenge case report and literature review</title><author>Jandou, Issam ; Moataz, Amine ; Mouqtassid, Mohammed Hicham ; Dakir, Mohammed ; Debbagh, Adil ; Aboutaieb, Rachid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-bbb4548b2bba8175b737c2d76ac00ac220aa1908c43daed36a6cd763fce052423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Bladder pheochromocytoma</topic><topic>Case Report</topic><topic>Ectopic pheochromocytoma</topic><topic>Methoxylated derivative</topic><topic>Partial cystectomy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jandou, Issam</creatorcontrib><creatorcontrib>Moataz, Amine</creatorcontrib><creatorcontrib>Mouqtassid, Mohammed Hicham</creatorcontrib><creatorcontrib>Dakir, Mohammed</creatorcontrib><creatorcontrib>Debbagh, Adil</creatorcontrib><creatorcontrib>Aboutaieb, Rachid</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of surgery case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jandou, Issam</au><au>Moataz, Amine</au><au>Mouqtassid, Mohammed Hicham</au><au>Dakir, Mohammed</au><au>Debbagh, Adil</au><au>Aboutaieb, Rachid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The ectopic vesical pheochromocytoma a diagnostic and therapeutic challenge case report and literature review</atitle><jtitle>International journal of surgery case reports</jtitle><addtitle>Int J Surg Case Rep</addtitle><date>2020-01-01</date><risdate>2020</risdate><volume>77</volume><spage>857</spage><epage>861</epage><pages>857-861</pages><issn>2210-2612</issn><eissn>2210-2612</eissn><abstract>•Pheochromocytoma is a tumor developed at the expense of chromaffin tissues.•Extra-adrenal localization of pheochromocytoma is rare.•The main problem with these tumors is to affirm their benignity or malignancy.•Ectopic pheochromocytomas have a malignant development once in two.•Ectopic pheochromocytoma presents a diagnostic and therapeutic dilemma.
Extra-adrenal localization of pheochromocytoma is rare. Its clinical revelation is paroxysmal but maybe in the form of permanent hypertension resistant to treatment. The main problem with these tumors is to affirm their benignity or malignancy, ectopic pheochromocytomas have a malignant development once in two.
We report the observation of a 39-year-old woman hypertensive on Amlodipine. She presents for sweating, headache, and palpation. The dosage of urinary metabolites revealed a marked increase in metanephrine and normetanephrine. Imagery had shown, at the expense of the left lateral wall of the bladder, a budding tissue formation with irregular contours which was significantly enhanced after injection of PDC. The diagnosis of an ectopic pheochromocytoma was accepted. The patient underwent a partial cystectomy, the postoperative consequences of which were unremarkable.
Threatening secretory syndromes are rare medical situations that require urgent management. Pheochromocytoma can be seen at any age from childhood to old age. The treatment of pheochromocytoma is surgical, once the stages of positive and topographic diagnosis have been carried out, the patient must be immediately entrusted to a team of trained surgeons and anesthetists. The prognosis remains unpredictable, hence the interest in prolonged monitoring.
Pheochromocytoma is a tumor developed at the expense of chromaffin tissues, extra-adrenal localizations exist, but remain rare. It is a pathology that presents a diagnostic and therapeutic dilemma in which patients require regular and prolonged postoperative monitoring to detect a possible metastasis or recurrence.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>33395912</pmid><doi>10.1016/j.ijscr.2020.11.132</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bladder pheochromocytoma Case Report Ectopic pheochromocytoma Methoxylated derivative Partial cystectomy |
title | The ectopic vesical pheochromocytoma a diagnostic and therapeutic challenge case report and literature review |
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