Common Presentation with Uncommon Diagnosis: Multifocal Epithelioid Hemangioendothelioma
A young female patient presenting with recurrent hemoptysis, neck swelling, and mediastinal mass mimicking lymphadenopathy was admitted to the Institute of Post Graduate Medical Education and Research and SSKM hospital, Kolkata, India. Clinical features, radiological studies, fibre optic bronchoscop...
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Veröffentlicht in: | Oman medical journal 2015-11, Vol.30 (6), p.477-481 |
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creator | Mitra , Ritabrata Kundu , Susmita Naskar , Bidisha Ghosh Misra , Swapnendu Biswas , Debabani |
description | A young female patient presenting with recurrent hemoptysis, neck swelling, and mediastinal
mass mimicking lymphadenopathy was admitted to the Institute of Post Graduate Medical
Education and Research and SSKM hospital, Kolkata, India. Clinical features, radiological
studies, fibre optic bronchoscopy, and fine needle aspiration cytology from the neck
swelling created a diagnostic dilemma until surgical resection and immunohistochemistry
reports confirmed the diagnosis of multifocal epithelioid hemangioendothelioma, a rare
vascular tumor with intermediate malignancy potential. Because it is a slow-progressing
disease and due to the non-availability of standard chemotherapy, the patient, and her
legal guardian, opted for palliative care only. She was asymptomatic for four years but
again presented with hemoptysis, reappearance of the neck swelling on the same side, and
a mediastinal mass compressing the superior vena cava and right pulmonary artery. This
report describes the diagnostic problems and therapeutic challenges in the management of
this rare tumor over a four-year follow-up period. The clinical course emphasizes the highly
unpredictable nature of this tumor. |
doi_str_mv | 10.5001/omj.2015.93 |
format | Article |
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mass mimicking lymphadenopathy was admitted to the Institute of Post Graduate Medical
Education and Research and SSKM hospital, Kolkata, India. Clinical features, radiological
studies, fibre optic bronchoscopy, and fine needle aspiration cytology from the neck
swelling created a diagnostic dilemma until surgical resection and immunohistochemistry
reports confirmed the diagnosis of multifocal epithelioid hemangioendothelioma, a rare
vascular tumor with intermediate malignancy potential. Because it is a slow-progressing
disease and due to the non-availability of standard chemotherapy, the patient, and her
legal guardian, opted for palliative care only. She was asymptomatic for four years but
again presented with hemoptysis, reappearance of the neck swelling on the same side, and
a mediastinal mass compressing the superior vena cava and right pulmonary artery. This
report describes the diagnostic problems and therapeutic challenges in the management of
this rare tumor over a four-year follow-up period. The clinical course emphasizes the highly
unpredictable nature of this tumor.</description><identifier>ISSN: 1999-768X</identifier><identifier>EISSN: 2070-5204</identifier><identifier>DOI: 10.5001/omj.2015.93</identifier><identifier>PMID: 26674363</identifier><language>eng</language><publisher>Muscat - Oman: Oman Medical Specialty Board</publisher><subject>ANGIOMA ; Case Report ; CHEMOTHERAPY ; DIAGNOSIS ; Epithelioid ; Hemangioendothelioma ; Hemoptysis ; LYMPHOMA ; MALIGNANT TUMOURS ; MEDICAL SCIENCES ; PATIENTS ; Vascular Neoplasms ; الأورام الخبيثة ; التشخيص ; العلاج الكيميائي ; العلوم الطبية ; المرضى ; الورم اللمفي ; الورم الوعائي</subject><ispartof>Oman medical journal, 2015-11, Vol.30 (6), p.477-481</ispartof><rights>2015 Oman Medical Specialty Board</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a3733-8ae48a3e8277e7c9d1694a1ab35c840f3fa3dc78f181893707a7a0aacb9277cf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://static.almanhal.com/covers/titl/73458/cover-lg.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678444/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678444/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26674363$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitra , Ritabrata</creatorcontrib><creatorcontrib>Kundu , Susmita</creatorcontrib><creatorcontrib>Naskar , Bidisha Ghosh</creatorcontrib><creatorcontrib>Misra , Swapnendu</creatorcontrib><creatorcontrib>Biswas , Debabani</creatorcontrib><title>Common Presentation with Uncommon Diagnosis: Multifocal Epithelioid Hemangioendothelioma</title><title>Oman medical journal</title><addtitle>Oman Med J</addtitle><description>A young female patient presenting with recurrent hemoptysis, neck swelling, and mediastinal
mass mimicking lymphadenopathy was admitted to the Institute of Post Graduate Medical
Education and Research and SSKM hospital, Kolkata, India. Clinical features, radiological
studies, fibre optic bronchoscopy, and fine needle aspiration cytology from the neck
swelling created a diagnostic dilemma until surgical resection and immunohistochemistry
reports confirmed the diagnosis of multifocal epithelioid hemangioendothelioma, a rare
vascular tumor with intermediate malignancy potential. Because it is a slow-progressing
disease and due to the non-availability of standard chemotherapy, the patient, and her
legal guardian, opted for palliative care only. She was asymptomatic for four years but
again presented with hemoptysis, reappearance of the neck swelling on the same side, and
a mediastinal mass compressing the superior vena cava and right pulmonary artery. This
report describes the diagnostic problems and therapeutic challenges in the management of
this rare tumor over a four-year follow-up period. The clinical course emphasizes the highly
unpredictable nature of this tumor.</description><subject>ANGIOMA</subject><subject>Case Report</subject><subject>CHEMOTHERAPY</subject><subject>DIAGNOSIS</subject><subject>Epithelioid</subject><subject>Hemangioendothelioma</subject><subject>Hemoptysis</subject><subject>LYMPHOMA</subject><subject>MALIGNANT TUMOURS</subject><subject>MEDICAL SCIENCES</subject><subject>PATIENTS</subject><subject>Vascular Neoplasms</subject><subject>الأورام الخبيثة</subject><subject>التشخيص</subject><subject>العلاج الكيميائي</subject><subject>العلوم الطبية</subject><subject>المرضى</subject><subject>الورم اللمفي</subject><subject>الورم الوعائي</subject><issn>1999-768X</issn><issn>2070-5204</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkc9LwzAUx4MobsydPCu7j84kL22SiyDzJwz04MBbeE3TraNtRjsV_3szq3PLJeR9v-_zknwJOWd0ElPKrny1mnDK4omGI9LnVNIo5lQckz7TWkcyUW89MmzbFQ0LNNfAT0mPJ4kUkECfjKe-qnw9emlc6-oNbopw-Cw2y9G8tp10W-Ci9m3RnpGTHMvWDX_3AZnf371OH6PZ88PT9GYWIUiASKETCsEpLqWTVmcs0QIZphBbJWgOOUJmpcqZYkqDpBIlUkSb6tBhcxiQp46beVyZdVNU2HwZj4X5KfhmYbDZFLZ0JkPHBbdpKlwsRJYrIVPOHNexpnGKLLCuO9b6Pa1cZsMbGywPoIdKXSzNwn8YkUglhAiAcQewjW_bxuW7XkbNNgITIjDbCIyG4L7cH7fz_n14MFx0BhfqLsedQ2oFWvzrWFZYL_euKkHECr4BI72V8w</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Mitra , Ritabrata</creator><creator>Kundu , Susmita</creator><creator>Naskar , Bidisha Ghosh</creator><creator>Misra , Swapnendu</creator><creator>Biswas , Debabani</creator><general>Oman Medical Specialty Board</general><general>OMJ</general><scope>~6Z</scope><scope>ADJCN</scope><scope>AHFXO</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20151101</creationdate><title>Common Presentation with Uncommon Diagnosis</title><author>Mitra , Ritabrata ; Kundu , Susmita ; Naskar , Bidisha Ghosh ; Misra , Swapnendu ; Biswas , Debabani</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a3733-8ae48a3e8277e7c9d1694a1ab35c840f3fa3dc78f181893707a7a0aacb9277cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>ANGIOMA</topic><topic>Case Report</topic><topic>CHEMOTHERAPY</topic><topic>DIAGNOSIS</topic><topic>Epithelioid</topic><topic>Hemangioendothelioma</topic><topic>Hemoptysis</topic><topic>LYMPHOMA</topic><topic>MALIGNANT TUMOURS</topic><topic>MEDICAL SCIENCES</topic><topic>PATIENTS</topic><topic>Vascular Neoplasms</topic><topic>الأورام الخبيثة</topic><topic>التشخيص</topic><topic>العلاج الكيميائي</topic><topic>العلوم الطبية</topic><topic>المرضى</topic><topic>الورم اللمفي</topic><topic>الورم الوعائي</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitra , Ritabrata</creatorcontrib><creatorcontrib>Kundu , Susmita</creatorcontrib><creatorcontrib>Naskar , Bidisha Ghosh</creatorcontrib><creatorcontrib>Misra , Swapnendu</creatorcontrib><creatorcontrib>Biswas , Debabani</creatorcontrib><collection>Al Manhal All Journals Collection</collection><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Oman medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitra , Ritabrata</au><au>Kundu , Susmita</au><au>Naskar , Bidisha Ghosh</au><au>Misra , Swapnendu</au><au>Biswas , Debabani</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Common Presentation with Uncommon Diagnosis: Multifocal Epithelioid Hemangioendothelioma</atitle><jtitle>Oman medical journal</jtitle><addtitle>Oman Med J</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>30</volume><issue>6</issue><spage>477</spage><epage>481</epage><pages>477-481</pages><issn>1999-768X</issn><eissn>2070-5204</eissn><abstract>A young female patient presenting with recurrent hemoptysis, neck swelling, and mediastinal
mass mimicking lymphadenopathy was admitted to the Institute of Post Graduate Medical
Education and Research and SSKM hospital, Kolkata, India. Clinical features, radiological
studies, fibre optic bronchoscopy, and fine needle aspiration cytology from the neck
swelling created a diagnostic dilemma until surgical resection and immunohistochemistry
reports confirmed the diagnosis of multifocal epithelioid hemangioendothelioma, a rare
vascular tumor with intermediate malignancy potential. Because it is a slow-progressing
disease and due to the non-availability of standard chemotherapy, the patient, and her
legal guardian, opted for palliative care only. She was asymptomatic for four years but
again presented with hemoptysis, reappearance of the neck swelling on the same side, and
a mediastinal mass compressing the superior vena cava and right pulmonary artery. This
report describes the diagnostic problems and therapeutic challenges in the management of
this rare tumor over a four-year follow-up period. The clinical course emphasizes the highly
unpredictable nature of this tumor.</abstract><cop>Muscat - Oman</cop><pub>Oman Medical Specialty Board</pub><pmid>26674363</pmid><doi>10.5001/omj.2015.93</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | ANGIOMA Case Report CHEMOTHERAPY DIAGNOSIS Epithelioid Hemangioendothelioma Hemoptysis LYMPHOMA MALIGNANT TUMOURS MEDICAL SCIENCES PATIENTS Vascular Neoplasms الأورام الخبيثة التشخيص العلاج الكيميائي العلوم الطبية المرضى الورم اللمفي الورم الوعائي |
title | Common Presentation with Uncommon Diagnosis: Multifocal Epithelioid Hemangioendothelioma |
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