Imaging findings of Kaposiform Hemangioendothelioma in children
Abstract Purpose Kaposiform hemangioendothelioma (KHE) is a rare, aggressive vascular tumor that typically occurs during infancy or early childhood. Though several case reports have discussed the imaging findings of KHE, larger comprehensive studies are lacking. The purpose of this study was to eval...
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description | Abstract Purpose Kaposiform hemangioendothelioma (KHE) is a rare, aggressive vascular tumor that typically occurs during infancy or early childhood. Though several case reports have discussed the imaging findings of KHE, larger comprehensive studies are lacking. The purpose of this study was to evaluate the imaging findings of KHE in children. Materials and methods A total of twelve cases of pathologically proven KHE were collected by searching our institution’s pathology database for children diagnosed between January 2004 and April 2016 (6 male, 6 female; median age: 3 months; age range 7 days − 18 years). CT (n = 7) and MRI (n = 9) findings were retrospectively evaluated. The location, morphology, enhancement, and growth pattern were analyzed. Results KHEs involved various locations: superficial or deep soft tissue of the extremities (n = 4); abdomen (n = 3; 2 cases, pancreas; 1 case, small bowel), neck and mediastinum (n = 1); chest wall, diaphragm, and pericardium (n = 1); abdominal wall (n = 1); and head (IAC, CP angle) (n = 2). Eight of 10 cases (80%) with CT/MR findings were locally invasive and involved two or more adjacent organs. Three cases presented as well-defined solid masses, and seven were associated with infiltrative lesions of the surrounding areas with (n = 4) or without definite solid regions (n = 3). In nine patients with MRI, all KHEs were heterogeneous and hyperintense to muscles on T2-weighted images (T2WI), while four KHEs consisted of some regions that were nearly isointense to muscle. Eight of the 10 cases with imaging exhibited heterogeneous intense enhancement, while only one demonstrated mild enhancement. Signal voids (n = 2), engorged vessels (n = 1), calcification (n = 3), hemorrhage (n = 1), or bone changes (n = 4) were infrequently observed. Four patients (33%) had Kasabach-Merritt phenomenon, and recurrence was observed in two cases. Conclusion KHEs occurred in various locations, affected mostly infants, and generally exhibited intense heterogeneous enhancement. In more than half of the included cases, KHEs were highly infiltrative and locally invasive with ill-defined margins. Awareness of these features should prompt radiologists to include KHE in the differential diagnosis for pediatric masses. |
doi_str_mv | 10.1016/j.ejrad.2016.11.015 |
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Though several case reports have discussed the imaging findings of KHE, larger comprehensive studies are lacking. The purpose of this study was to evaluate the imaging findings of KHE in children. Materials and methods A total of twelve cases of pathologically proven KHE were collected by searching our institution’s pathology database for children diagnosed between January 2004 and April 2016 (6 male, 6 female; median age: 3 months; age range 7 days − 18 years). CT (n = 7) and MRI (n = 9) findings were retrospectively evaluated. The location, morphology, enhancement, and growth pattern were analyzed. Results KHEs involved various locations: superficial or deep soft tissue of the extremities (n = 4); abdomen (n = 3; 2 cases, pancreas; 1 case, small bowel), neck and mediastinum (n = 1); chest wall, diaphragm, and pericardium (n = 1); abdominal wall (n = 1); and head (IAC, CP angle) (n = 2). Eight of 10 cases (80%) with CT/MR findings were locally invasive and involved two or more adjacent organs. Three cases presented as well-defined solid masses, and seven were associated with infiltrative lesions of the surrounding areas with (n = 4) or without definite solid regions (n = 3). In nine patients with MRI, all KHEs were heterogeneous and hyperintense to muscles on T2-weighted images (T2WI), while four KHEs consisted of some regions that were nearly isointense to muscle. Eight of the 10 cases with imaging exhibited heterogeneous intense enhancement, while only one demonstrated mild enhancement. Signal voids (n = 2), engorged vessels (n = 1), calcification (n = 3), hemorrhage (n = 1), or bone changes (n = 4) were infrequently observed. Four patients (33%) had Kasabach-Merritt phenomenon, and recurrence was observed in two cases. Conclusion KHEs occurred in various locations, affected mostly infants, and generally exhibited intense heterogeneous enhancement. In more than half of the included cases, KHEs were highly infiltrative and locally invasive with ill-defined margins. Awareness of these features should prompt radiologists to include KHE in the differential diagnosis for pediatric masses.</description><identifier>ISSN: 0720-048X</identifier><identifier>EISSN: 1872-7727</identifier><identifier>DOI: 10.1016/j.ejrad.2016.11.015</identifier><identifier>PMID: 28027747</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Adolescent ; Child ; Child, Preschool ; Diagnosis, Differential ; Female ; Head and Neck Neoplasms - pathology ; Hemangioendothelioma - pathology ; Humans ; Infant ; Infant, Newborn ; Kaposiform hemangioendothelioma ; Kasabach-Merritt phenomenon ; Kasabach-Merritt Syndrome - pathology ; Magnetic Resonance Imaging ; Male ; Multimodal Imaging ; Neoplasm Recurrence, Local - pathology ; Radiology ; Retrospective Studies ; Sarcoma, Kaposi - pathology ; Skin Neoplasms - pathology ; Tomography, X-Ray Computed ; Vascular Neoplasms - pathology ; Vascular tumor</subject><ispartof>European journal of radiology, 2017-01, Vol.86, p.198-205</ispartof><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-6e98672f4c9b06a35680c14c945b8bf1f177c2ff18fc476359618890023e9c033</citedby><cites>FETCH-LOGICAL-c414t-6e98672f4c9b06a35680c14c945b8bf1f177c2ff18fc476359618890023e9c033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejrad.2016.11.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3541,27915,27916,45986</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28027747$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jin Ryu, Young</creatorcontrib><creatorcontrib>Choi, Young Hun</creatorcontrib><creatorcontrib>Cheon, Jung-Eun</creatorcontrib><creatorcontrib>Kim, Woo Sun</creatorcontrib><creatorcontrib>Kim, In-One</creatorcontrib><creatorcontrib>Park, Ji Eun</creatorcontrib><creatorcontrib>Kim, Yu Jin</creatorcontrib><title>Imaging findings of Kaposiform Hemangioendothelioma in children</title><title>European journal of radiology</title><addtitle>Eur J Radiol</addtitle><description>Abstract Purpose Kaposiform hemangioendothelioma (KHE) is a rare, aggressive vascular tumor that typically occurs during infancy or early childhood. Though several case reports have discussed the imaging findings of KHE, larger comprehensive studies are lacking. The purpose of this study was to evaluate the imaging findings of KHE in children. Materials and methods A total of twelve cases of pathologically proven KHE were collected by searching our institution’s pathology database for children diagnosed between January 2004 and April 2016 (6 male, 6 female; median age: 3 months; age range 7 days − 18 years). CT (n = 7) and MRI (n = 9) findings were retrospectively evaluated. The location, morphology, enhancement, and growth pattern were analyzed. Results KHEs involved various locations: superficial or deep soft tissue of the extremities (n = 4); abdomen (n = 3; 2 cases, pancreas; 1 case, small bowel), neck and mediastinum (n = 1); chest wall, diaphragm, and pericardium (n = 1); abdominal wall (n = 1); and head (IAC, CP angle) (n = 2). Eight of 10 cases (80%) with CT/MR findings were locally invasive and involved two or more adjacent organs. Three cases presented as well-defined solid masses, and seven were associated with infiltrative lesions of the surrounding areas with (n = 4) or without definite solid regions (n = 3). In nine patients with MRI, all KHEs were heterogeneous and hyperintense to muscles on T2-weighted images (T2WI), while four KHEs consisted of some regions that were nearly isointense to muscle. Eight of the 10 cases with imaging exhibited heterogeneous intense enhancement, while only one demonstrated mild enhancement. Signal voids (n = 2), engorged vessels (n = 1), calcification (n = 3), hemorrhage (n = 1), or bone changes (n = 4) were infrequently observed. Four patients (33%) had Kasabach-Merritt phenomenon, and recurrence was observed in two cases. Conclusion KHEs occurred in various locations, affected mostly infants, and generally exhibited intense heterogeneous enhancement. In more than half of the included cases, KHEs were highly infiltrative and locally invasive with ill-defined margins. Awareness of these features should prompt radiologists to include KHE in the differential diagnosis for pediatric masses.</description><subject>Adolescent</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>Hemangioendothelioma - pathology</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Kaposiform hemangioendothelioma</subject><subject>Kasabach-Merritt phenomenon</subject><subject>Kasabach-Merritt Syndrome - pathology</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Multimodal Imaging</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Radiology</subject><subject>Retrospective Studies</subject><subject>Sarcoma, Kaposi - pathology</subject><subject>Skin Neoplasms - pathology</subject><subject>Tomography, X-Ray Computed</subject><subject>Vascular Neoplasms - pathology</subject><subject>Vascular tumor</subject><issn>0720-048X</issn><issn>1872-7727</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EokvhFyChHLkkeGzHdg6AqgpoRaUeChI3y-uMtw6Jvdi7lfrv8bKFA5eenkZ6b57mG0JeA-2Agnw3dThlO3asDh1AR6F_QlagFWuVYuopWVHFaEuF_nFCXpQyUUp7MbDn5IRpypQSakU-Xi52E-Km8SGOVUuTfPPVblMJPuWlucDFxk1IGMe0u8U5pMU2ITbuNsxjxviSPPN2LvjqQU_J98-fvp1ftFfXXy7Pz65aJ0DsWomDlop54YY1lZb3UlMHdRL9Wq89eFDKMe9BeyeU5P0gQeuBUsZxcJTzU_L2uHeb0689lp1ZQnE4zzZi2hcDuudKCNnrauVHq8uplIzebHNYbL43QM2BnJnMH3LmQM4AmEqupt48FOzXC47_Mn9RVcP7owHrmXcBsykuYHQ4hoxuZ8YUHin48F_ezSEGZ-efeI9lSvscK0EDpjBDzc3heYffgeSUS6n4b96Qk7Q</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Jin Ryu, Young</creator><creator>Choi, Young Hun</creator><creator>Cheon, Jung-Eun</creator><creator>Kim, Woo Sun</creator><creator>Kim, In-One</creator><creator>Park, Ji Eun</creator><creator>Kim, Yu Jin</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>20170101</creationdate><title>Imaging findings of Kaposiform Hemangioendothelioma in children</title><author>Jin Ryu, Young ; Choi, Young Hun ; Cheon, Jung-Eun ; Kim, Woo Sun ; Kim, In-One ; Park, Ji Eun ; Kim, Yu Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-6e98672f4c9b06a35680c14c945b8bf1f177c2ff18fc476359618890023e9c033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Head and Neck Neoplasms - pathology</topic><topic>Hemangioendothelioma - pathology</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Kaposiform hemangioendothelioma</topic><topic>Kasabach-Merritt phenomenon</topic><topic>Kasabach-Merritt Syndrome - pathology</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Multimodal Imaging</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Radiology</topic><topic>Retrospective Studies</topic><topic>Sarcoma, Kaposi - pathology</topic><topic>Skin Neoplasms - pathology</topic><topic>Tomography, X-Ray Computed</topic><topic>Vascular Neoplasms - pathology</topic><topic>Vascular tumor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jin Ryu, Young</creatorcontrib><creatorcontrib>Choi, Young Hun</creatorcontrib><creatorcontrib>Cheon, Jung-Eun</creatorcontrib><creatorcontrib>Kim, Woo Sun</creatorcontrib><creatorcontrib>Kim, In-One</creatorcontrib><creatorcontrib>Park, Ji Eun</creatorcontrib><creatorcontrib>Kim, Yu Jin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of radiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jin Ryu, Young</au><au>Choi, Young Hun</au><au>Cheon, Jung-Eun</au><au>Kim, Woo Sun</au><au>Kim, In-One</au><au>Park, Ji Eun</au><au>Kim, Yu Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Imaging findings of Kaposiform Hemangioendothelioma in children</atitle><jtitle>European journal of radiology</jtitle><addtitle>Eur J Radiol</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>86</volume><spage>198</spage><epage>205</epage><pages>198-205</pages><issn>0720-048X</issn><eissn>1872-7727</eissn><abstract>Abstract Purpose Kaposiform hemangioendothelioma (KHE) is a rare, aggressive vascular tumor that typically occurs during infancy or early childhood. Though several case reports have discussed the imaging findings of KHE, larger comprehensive studies are lacking. The purpose of this study was to evaluate the imaging findings of KHE in children. Materials and methods A total of twelve cases of pathologically proven KHE were collected by searching our institution’s pathology database for children diagnosed between January 2004 and April 2016 (6 male, 6 female; median age: 3 months; age range 7 days − 18 years). CT (n = 7) and MRI (n = 9) findings were retrospectively evaluated. The location, morphology, enhancement, and growth pattern were analyzed. Results KHEs involved various locations: superficial or deep soft tissue of the extremities (n = 4); abdomen (n = 3; 2 cases, pancreas; 1 case, small bowel), neck and mediastinum (n = 1); chest wall, diaphragm, and pericardium (n = 1); abdominal wall (n = 1); and head (IAC, CP angle) (n = 2). Eight of 10 cases (80%) with CT/MR findings were locally invasive and involved two or more adjacent organs. Three cases presented as well-defined solid masses, and seven were associated with infiltrative lesions of the surrounding areas with (n = 4) or without definite solid regions (n = 3). In nine patients with MRI, all KHEs were heterogeneous and hyperintense to muscles on T2-weighted images (T2WI), while four KHEs consisted of some regions that were nearly isointense to muscle. Eight of the 10 cases with imaging exhibited heterogeneous intense enhancement, while only one demonstrated mild enhancement. Signal voids (n = 2), engorged vessels (n = 1), calcification (n = 3), hemorrhage (n = 1), or bone changes (n = 4) were infrequently observed. Four patients (33%) had Kasabach-Merritt phenomenon, and recurrence was observed in two cases. Conclusion KHEs occurred in various locations, affected mostly infants, and generally exhibited intense heterogeneous enhancement. In more than half of the included cases, KHEs were highly infiltrative and locally invasive with ill-defined margins. Awareness of these features should prompt radiologists to include KHE in the differential diagnosis for pediatric masses.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>28027747</pmid><doi>10.1016/j.ejrad.2016.11.015</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Child Child, Preschool Diagnosis, Differential Female Head and Neck Neoplasms - pathology Hemangioendothelioma - pathology Humans Infant Infant, Newborn Kaposiform hemangioendothelioma Kasabach-Merritt phenomenon Kasabach-Merritt Syndrome - pathology Magnetic Resonance Imaging Male Multimodal Imaging Neoplasm Recurrence, Local - pathology Radiology Retrospective Studies Sarcoma, Kaposi - pathology Skin Neoplasms - pathology Tomography, X-Ray Computed Vascular Neoplasms - pathology Vascular tumor |
title | Imaging findings of Kaposiform Hemangioendothelioma in children |
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