Vascular invasion in uterine sarcomas and its significance. A multi-institutional study
Summary Although metastases and high-mortality are frequent in high-grade endometrial sarcomas (HGSs), these findings are less commonly seen in low-grade endometrial stromal sarcomas (LGESSs), even in cases with lymphovascular invasion (LVI). We hypothesized that the “bulging plugs” of tumor charact...
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creator | Roma, Andres A., MD Barbuto, Denise A., MD Samimi, Siavash Azadmanesh, MD Stolnicu, Simona, MD Alvarado-Cabrero, Isabel, MD Chanona-Vilchis, Jose, MD Aguilera-Barrantes, Irene, MD de Peralta-Venturina, Mariza, MD Malpica, Anais, MD Rutgers, Joanne K.L., MD Silva, Elvio G., MD |
description | Summary Although metastases and high-mortality are frequent in high-grade endometrial sarcomas (HGSs), these findings are less commonly seen in low-grade endometrial stromal sarcomas (LGESSs), even in cases with lymphovascular invasion (LVI). We hypothesized that the “bulging plugs” of tumor characteristic of LVI in LGESS are fundamentally different from LVI seen in HGS. We reviewed 70 uterine sarcomas: 42 HGSs (high-grade endometrial stromal sarcomas, undifferentiated uterine sarcoma, and leiomyosarcoma) and 28 LGESSs. All cases had LVI documented on the histologic slides. Immunostains for CD31, ERG, and D2-40 were performed. LGESS harbored cohesive intravascular tumor foci with direct communication from the main tumor and attached to the vessel wall. The intravascular foci included tumor cells and small arteriole-type vessels and were surrounded by a thin fibrous band. Vascular markers confirmed the LVI and highlighted positively stained endothelial cells separating intravascular tumor foci from the blood itself. In contrast, intravascular tumor foci in HGS were composed of discohesive cells clusters, lacking the features described in LGESS. Only 8 (30.8%) patients with LGESS had recurrence/metastases (6 with lung metastasis); only 1 patient died of disease. Thirty (77%) patients with HGS had recurrence/metastases, 27 (69%) patients had lung metastases, and 22 (56.4%) patients died of disease. We propose that in most LGESSs, LVI represents vascular intrusion; manipulation or trauma is potentially responsible for tumor cell detachment into the circulation increasing the chances of recurrence/metastases. Classic LVI features were identified in HGS. This important distinction may allow for better management of patients and avoid unnecessary treatment in LGESS, reducing morbidity. |
doi_str_mv | 10.1016/j.humpath.2015.07.011 |
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A multi-institutional study</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Roma, Andres A., MD ; Barbuto, Denise A., MD ; Samimi, Siavash Azadmanesh, MD ; Stolnicu, Simona, MD ; Alvarado-Cabrero, Isabel, MD ; Chanona-Vilchis, Jose, MD ; Aguilera-Barrantes, Irene, MD ; de Peralta-Venturina, Mariza, MD ; Malpica, Anais, MD ; Rutgers, Joanne K.L., MD ; Silva, Elvio G., MD</creator><creatorcontrib>Roma, Andres A., MD ; Barbuto, Denise A., MD ; Samimi, Siavash Azadmanesh, MD ; Stolnicu, Simona, MD ; Alvarado-Cabrero, Isabel, MD ; Chanona-Vilchis, Jose, MD ; Aguilera-Barrantes, Irene, MD ; de Peralta-Venturina, Mariza, MD ; Malpica, Anais, MD ; Rutgers, Joanne K.L., MD ; Silva, Elvio G., MD</creatorcontrib><description>Summary Although metastases and high-mortality are frequent in high-grade endometrial sarcomas (HGSs), these findings are less commonly seen in low-grade endometrial stromal sarcomas (LGESSs), even in cases with lymphovascular invasion (LVI). We hypothesized that the “bulging plugs” of tumor characteristic of LVI in LGESS are fundamentally different from LVI seen in HGS. We reviewed 70 uterine sarcomas: 42 HGSs (high-grade endometrial stromal sarcomas, undifferentiated uterine sarcoma, and leiomyosarcoma) and 28 LGESSs. All cases had LVI documented on the histologic slides. Immunostains for CD31, ERG, and D2-40 were performed. LGESS harbored cohesive intravascular tumor foci with direct communication from the main tumor and attached to the vessel wall. The intravascular foci included tumor cells and small arteriole-type vessels and were surrounded by a thin fibrous band. Vascular markers confirmed the LVI and highlighted positively stained endothelial cells separating intravascular tumor foci from the blood itself. In contrast, intravascular tumor foci in HGS were composed of discohesive cells clusters, lacking the features described in LGESS. Only 8 (30.8%) patients with LGESS had recurrence/metastases (6 with lung metastasis); only 1 patient died of disease. Thirty (77%) patients with HGS had recurrence/metastases, 27 (69%) patients had lung metastases, and 22 (56.4%) patients died of disease. We propose that in most LGESSs, LVI represents vascular intrusion; manipulation or trauma is potentially responsible for tumor cell detachment into the circulation increasing the chances of recurrence/metastases. Classic LVI features were identified in HGS. This important distinction may allow for better management of patients and avoid unnecessary treatment in LGESS, reducing morbidity.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2015.07.011</identifier><identifier>PMID: 26410057</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Abdomen ; Adult ; Age ; Aged ; Aged, 80 and over ; Breast cancer ; Chemotherapy ; Endometrial Neoplasms - pathology ; Female ; Humans ; Leiomyosarcoma ; Low-grade endometrial stromal sarcomas ; Lymphatic system ; Lymphvascular invasion ; Medical prognosis ; Metastasis ; Middle Aged ; Neoplasm Recurrence, Local - pathology ; Neovascularization, Pathologic - pathology ; Pathology ; Sarcoma - pathology ; Sarcoma, Endometrial Stromal - pathology ; Tumors ; Undifferentiated uterine sarcoma ; Uterine cancer ; Uterine Neoplasms - pathology ; Uterine sarcoma</subject><ispartof>Human pathology, 2015-11, Vol.46 (11), p.1712-1721</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Nov 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-4a6c3c735ab9c57994f596b45aac3bd88ed1c36fee7ed5cdb2b209c3b4dca12f3</citedby><cites>FETCH-LOGICAL-c448t-4a6c3c735ab9c57994f596b45aac3bd88ed1c36fee7ed5cdb2b209c3b4dca12f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.humpath.2015.07.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26410057$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roma, Andres A., MD</creatorcontrib><creatorcontrib>Barbuto, Denise A., MD</creatorcontrib><creatorcontrib>Samimi, Siavash Azadmanesh, MD</creatorcontrib><creatorcontrib>Stolnicu, Simona, MD</creatorcontrib><creatorcontrib>Alvarado-Cabrero, Isabel, MD</creatorcontrib><creatorcontrib>Chanona-Vilchis, Jose, MD</creatorcontrib><creatorcontrib>Aguilera-Barrantes, Irene, MD</creatorcontrib><creatorcontrib>de Peralta-Venturina, Mariza, MD</creatorcontrib><creatorcontrib>Malpica, Anais, MD</creatorcontrib><creatorcontrib>Rutgers, Joanne K.L., MD</creatorcontrib><creatorcontrib>Silva, Elvio G., MD</creatorcontrib><title>Vascular invasion in uterine sarcomas and its significance. A multi-institutional study</title><title>Human pathology</title><addtitle>Hum Pathol</addtitle><description>Summary Although metastases and high-mortality are frequent in high-grade endometrial sarcomas (HGSs), these findings are less commonly seen in low-grade endometrial stromal sarcomas (LGESSs), even in cases with lymphovascular invasion (LVI). We hypothesized that the “bulging plugs” of tumor characteristic of LVI in LGESS are fundamentally different from LVI seen in HGS. We reviewed 70 uterine sarcomas: 42 HGSs (high-grade endometrial stromal sarcomas, undifferentiated uterine sarcoma, and leiomyosarcoma) and 28 LGESSs. All cases had LVI documented on the histologic slides. Immunostains for CD31, ERG, and D2-40 were performed. LGESS harbored cohesive intravascular tumor foci with direct communication from the main tumor and attached to the vessel wall. The intravascular foci included tumor cells and small arteriole-type vessels and were surrounded by a thin fibrous band. Vascular markers confirmed the LVI and highlighted positively stained endothelial cells separating intravascular tumor foci from the blood itself. In contrast, intravascular tumor foci in HGS were composed of discohesive cells clusters, lacking the features described in LGESS. Only 8 (30.8%) patients with LGESS had recurrence/metastases (6 with lung metastasis); only 1 patient died of disease. Thirty (77%) patients with HGS had recurrence/metastases, 27 (69%) patients had lung metastases, and 22 (56.4%) patients died of disease. We propose that in most LGESSs, LVI represents vascular intrusion; manipulation or trauma is potentially responsible for tumor cell detachment into the circulation increasing the chances of recurrence/metastases. Classic LVI features were identified in HGS. This important distinction may allow for better management of patients and avoid unnecessary treatment in LGESS, reducing morbidity.</description><subject>Abdomen</subject><subject>Adult</subject><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Breast cancer</subject><subject>Chemotherapy</subject><subject>Endometrial Neoplasms - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Leiomyosarcoma</subject><subject>Low-grade endometrial stromal sarcomas</subject><subject>Lymphatic system</subject><subject>Lymphvascular invasion</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neovascularization, Pathologic - pathology</subject><subject>Pathology</subject><subject>Sarcoma - pathology</subject><subject>Sarcoma, Endometrial Stromal - pathology</subject><subject>Tumors</subject><subject>Undifferentiated uterine sarcoma</subject><subject>Uterine cancer</subject><subject>Uterine Neoplasms - pathology</subject><subject>Uterine sarcoma</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1vFSEUhonR2NvqT9BM4sbNjMAMMLPRNI2tJk1ctOqSMHDGcp2PKwea3H9fxnvVpBtXkPC8L_AcQl4xWjHK5LttdZemnYl3FadMVFRVlLEnZMNEzcu27vhTsqG0kWXLlDohp4hbmgnRiOfkhMuGUSrUhnz_ZtCm0YTCz_cG_TLnTZEiBD9DgSbYZTJYmNkVPmKB_sfsB2_NbKEqzospjdGXfsboY4o5bcYCY3L7F-TZYEaEl8f1jHy9_Hh78am8_nL1-eL8urRN08ayMdLWVtXC9J0VquuaQXSyb4Qxtu5d24JjtpYDgAInrOt5z2mXjxpnDeNDfUbeHnp3YfmVAKOePFoYRzPDklAzVUupWsG6jL55hG6XFPKLV4q3kin5mxIHyoYFMcCgd8FPJuw1o3o1r7f6aF6v5jVVOnvNudfH9tRP4P6m_qjOwIcDAFnHvYeg0XrIHp0PYKN2i__vFe8fNdjRz3kY40_YA_77jUauqb5Zx79OnwlKueh4_QCakq1n</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Roma, Andres A., MD</creator><creator>Barbuto, Denise A., MD</creator><creator>Samimi, Siavash Azadmanesh, MD</creator><creator>Stolnicu, Simona, MD</creator><creator>Alvarado-Cabrero, Isabel, MD</creator><creator>Chanona-Vilchis, Jose, MD</creator><creator>Aguilera-Barrantes, Irene, MD</creator><creator>de Peralta-Venturina, Mariza, MD</creator><creator>Malpica, Anais, MD</creator><creator>Rutgers, Joanne K.L., MD</creator><creator>Silva, Elvio G., MD</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>K9.</scope><scope>7X8</scope></search><sort><creationdate>20151101</creationdate><title>Vascular invasion in uterine sarcomas and its significance. A multi-institutional study</title><author>Roma, Andres A., MD ; Barbuto, Denise A., MD ; Samimi, Siavash Azadmanesh, MD ; Stolnicu, Simona, MD ; Alvarado-Cabrero, Isabel, MD ; Chanona-Vilchis, Jose, MD ; Aguilera-Barrantes, Irene, MD ; de Peralta-Venturina, Mariza, MD ; Malpica, Anais, MD ; Rutgers, Joanne K.L., MD ; Silva, Elvio G., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-4a6c3c735ab9c57994f596b45aac3bd88ed1c36fee7ed5cdb2b209c3b4dca12f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Abdomen</topic><topic>Adult</topic><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Breast cancer</topic><topic>Chemotherapy</topic><topic>Endometrial Neoplasms - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Leiomyosarcoma</topic><topic>Low-grade endometrial stromal sarcomas</topic><topic>Lymphatic system</topic><topic>Lymphvascular invasion</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neovascularization, Pathologic - pathology</topic><topic>Pathology</topic><topic>Sarcoma - pathology</topic><topic>Sarcoma, Endometrial Stromal - pathology</topic><topic>Tumors</topic><topic>Undifferentiated uterine sarcoma</topic><topic>Uterine cancer</topic><topic>Uterine Neoplasms - pathology</topic><topic>Uterine sarcoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roma, Andres A., MD</creatorcontrib><creatorcontrib>Barbuto, Denise A., MD</creatorcontrib><creatorcontrib>Samimi, Siavash Azadmanesh, MD</creatorcontrib><creatorcontrib>Stolnicu, Simona, MD</creatorcontrib><creatorcontrib>Alvarado-Cabrero, Isabel, MD</creatorcontrib><creatorcontrib>Chanona-Vilchis, Jose, MD</creatorcontrib><creatorcontrib>Aguilera-Barrantes, Irene, MD</creatorcontrib><creatorcontrib>de Peralta-Venturina, Mariza, MD</creatorcontrib><creatorcontrib>Malpica, Anais, MD</creatorcontrib><creatorcontrib>Rutgers, Joanne K.L., MD</creatorcontrib><creatorcontrib>Silva, Elvio G., MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roma, Andres A., MD</au><au>Barbuto, Denise A., MD</au><au>Samimi, Siavash Azadmanesh, MD</au><au>Stolnicu, Simona, MD</au><au>Alvarado-Cabrero, Isabel, MD</au><au>Chanona-Vilchis, Jose, MD</au><au>Aguilera-Barrantes, Irene, MD</au><au>de Peralta-Venturina, Mariza, MD</au><au>Malpica, Anais, MD</au><au>Rutgers, Joanne K.L., MD</au><au>Silva, Elvio G., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vascular invasion in uterine sarcomas and its significance. A multi-institutional study</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>46</volume><issue>11</issue><spage>1712</spage><epage>1721</epage><pages>1712-1721</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><abstract>Summary Although metastases and high-mortality are frequent in high-grade endometrial sarcomas (HGSs), these findings are less commonly seen in low-grade endometrial stromal sarcomas (LGESSs), even in cases with lymphovascular invasion (LVI). We hypothesized that the “bulging plugs” of tumor characteristic of LVI in LGESS are fundamentally different from LVI seen in HGS. We reviewed 70 uterine sarcomas: 42 HGSs (high-grade endometrial stromal sarcomas, undifferentiated uterine sarcoma, and leiomyosarcoma) and 28 LGESSs. All cases had LVI documented on the histologic slides. Immunostains for CD31, ERG, and D2-40 were performed. LGESS harbored cohesive intravascular tumor foci with direct communication from the main tumor and attached to the vessel wall. The intravascular foci included tumor cells and small arteriole-type vessels and were surrounded by a thin fibrous band. Vascular markers confirmed the LVI and highlighted positively stained endothelial cells separating intravascular tumor foci from the blood itself. In contrast, intravascular tumor foci in HGS were composed of discohesive cells clusters, lacking the features described in LGESS. Only 8 (30.8%) patients with LGESS had recurrence/metastases (6 with lung metastasis); only 1 patient died of disease. Thirty (77%) patients with HGS had recurrence/metastases, 27 (69%) patients had lung metastases, and 22 (56.4%) patients died of disease. We propose that in most LGESSs, LVI represents vascular intrusion; manipulation or trauma is potentially responsible for tumor cell detachment into the circulation increasing the chances of recurrence/metastases. Classic LVI features were identified in HGS. This important distinction may allow for better management of patients and avoid unnecessary treatment in LGESS, reducing morbidity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26410057</pmid><doi>10.1016/j.humpath.2015.07.011</doi><tpages>10</tpages></addata></record> |
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subjects | Abdomen Adult Age Aged Aged, 80 and over Breast cancer Chemotherapy Endometrial Neoplasms - pathology Female Humans Leiomyosarcoma Low-grade endometrial stromal sarcomas Lymphatic system Lymphvascular invasion Medical prognosis Metastasis Middle Aged Neoplasm Recurrence, Local - pathology Neovascularization, Pathologic - pathology Pathology Sarcoma - pathology Sarcoma, Endometrial Stromal - pathology Tumors Undifferentiated uterine sarcoma Uterine cancer Uterine Neoplasms - pathology Uterine sarcoma |
title | Vascular invasion in uterine sarcomas and its significance. A multi-institutional study |
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