Multidisciplinary therapeutic strategy with appropriate timing and modalities for treating cervicofacial lymphatic malformations in children
Purpose The study reviewed a multidisciplinary approach to treating cervicofacial lymphatic malformations (CFLMs) in children. Methods Between 2007 and 2023, 53 children with CFLMs were treated with the median on-set age of 5 months (0–165) at our institute. For infants, airway management, including...
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creator | Suzuki, Kento Fumino, Shigehisa Iguchi, Masafumi Takayama, Shohei Kim, Kiyokazu Hirano, Shigeru Ono, Shigeru |
description | Purpose
The study reviewed a multidisciplinary approach to treating cervicofacial lymphatic malformations (CFLMs) in children.
Methods
Between 2007 and 2023, 53 children with CFLMs were treated with the median on-set age of 5 months (0–165) at our institute. For infants, airway management, including possible tracheotomy was prioritized, and a “wait-and-see” policy was adopted to expect spontaneous regression. Once children reached one year of age or diagnosed after infancy, OK-432 sclerotherapy and surgical treatment with/without sirolimus were considered for residual lesions.
Results
The median follow-up period was 38 months (0–169). Among 30 infants, tracheostomy was performed in 4 patients, with 3 successfully closed after treatment. Thirteen patients showed excellent improvement without treatment. Sclerotherapy was performed in 15 patients, and partial resection in 5. Six patients were treated with sirolimus and showed moderate shrinkage or cessation of bleeding. Overall, 23 of 30 infants showed moderate to excellent improvement. For the 23 patients diagnosed after infancy, 16 improved without treatment, and 7 showed moderate to excellent improvement with sclerotherapy.
Conclusions
The study concluded that early sclerotherapy for infants, particularly around the airway, poses risks, and tracheostomy might be necessary. The comprehensive strategy including "wait-and-see," sclerotherapy, sirolimus treatment, and timely surgery significantly improved the patients' quality of life. |
doi_str_mv | 10.1007/s00383-024-05947-y |
format | Article |
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The study reviewed a multidisciplinary approach to treating cervicofacial lymphatic malformations (CFLMs) in children.
Methods
Between 2007 and 2023, 53 children with CFLMs were treated with the median on-set age of 5 months (0–165) at our institute. For infants, airway management, including possible tracheotomy was prioritized, and a “wait-and-see” policy was adopted to expect spontaneous regression. Once children reached one year of age or diagnosed after infancy, OK-432 sclerotherapy and surgical treatment with/without sirolimus were considered for residual lesions.
Results
The median follow-up period was 38 months (0–169). Among 30 infants, tracheostomy was performed in 4 patients, with 3 successfully closed after treatment. Thirteen patients showed excellent improvement without treatment. Sclerotherapy was performed in 15 patients, and partial resection in 5. Six patients were treated with sirolimus and showed moderate shrinkage or cessation of bleeding. Overall, 23 of 30 infants showed moderate to excellent improvement. For the 23 patients diagnosed after infancy, 16 improved without treatment, and 7 showed moderate to excellent improvement with sclerotherapy.
Conclusions
The study concluded that early sclerotherapy for infants, particularly around the airway, poses risks, and tracheostomy might be necessary. The comprehensive strategy including "wait-and-see," sclerotherapy, sirolimus treatment, and timely surgery significantly improved the patients' quality of life.</description><identifier>ISSN: 0179-0358</identifier><identifier>ISSN: 1437-9813</identifier><identifier>EISSN: 1437-9813</identifier><identifier>DOI: 10.1007/s00383-024-05947-y</identifier><identifier>PMID: 39699633</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescent ; Child ; Child, Preschool ; Combined Modality Therapy ; Face - abnormalities ; Female ; Follow-Up Studies ; Humans ; Infant ; Infant, Newborn ; Lymphatic Abnormalities - therapy ; Male ; Medicine ; Medicine & Public Health ; Neck - abnormalities ; Original Article ; Ostomy ; Pediatric Surgery ; Pediatrics ; Picibanil - therapeutic use ; Retrospective Studies ; Sclerotherapy ; Sclerotherapy - methods ; Sirolimus - therapeutic use ; Surgery ; Tracheostomy ; Tracheotomy ; Treatment Outcome</subject><ispartof>Pediatric surgery international, 2024-12, Vol.41 (1), p.35</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024 Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><rights>Copyright Springer Nature B.V. Dec 2025</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00383-024-05947-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00383-024-05947-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39699633$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suzuki, Kento</creatorcontrib><creatorcontrib>Fumino, Shigehisa</creatorcontrib><creatorcontrib>Iguchi, Masafumi</creatorcontrib><creatorcontrib>Takayama, Shohei</creatorcontrib><creatorcontrib>Kim, Kiyokazu</creatorcontrib><creatorcontrib>Hirano, Shigeru</creatorcontrib><creatorcontrib>Ono, Shigeru</creatorcontrib><title>Multidisciplinary therapeutic strategy with appropriate timing and modalities for treating cervicofacial lymphatic malformations in children</title><title>Pediatric surgery international</title><addtitle>Pediatr Surg Int</addtitle><addtitle>Pediatr Surg Int</addtitle><description>Purpose
The study reviewed a multidisciplinary approach to treating cervicofacial lymphatic malformations (CFLMs) in children.
Methods
Between 2007 and 2023, 53 children with CFLMs were treated with the median on-set age of 5 months (0–165) at our institute. For infants, airway management, including possible tracheotomy was prioritized, and a “wait-and-see” policy was adopted to expect spontaneous regression. Once children reached one year of age or diagnosed after infancy, OK-432 sclerotherapy and surgical treatment with/without sirolimus were considered for residual lesions.
Results
The median follow-up period was 38 months (0–169). Among 30 infants, tracheostomy was performed in 4 patients, with 3 successfully closed after treatment. Thirteen patients showed excellent improvement without treatment. Sclerotherapy was performed in 15 patients, and partial resection in 5. Six patients were treated with sirolimus and showed moderate shrinkage or cessation of bleeding. Overall, 23 of 30 infants showed moderate to excellent improvement. For the 23 patients diagnosed after infancy, 16 improved without treatment, and 7 showed moderate to excellent improvement with sclerotherapy.
Conclusions
The study concluded that early sclerotherapy for infants, particularly around the airway, poses risks, and tracheostomy might be necessary. The comprehensive strategy including "wait-and-see," sclerotherapy, sirolimus treatment, and timely surgery significantly improved the patients' quality of life.</description><subject>Adolescent</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Combined Modality Therapy</subject><subject>Face - abnormalities</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Lymphatic Abnormalities - therapy</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neck - abnormalities</subject><subject>Original Article</subject><subject>Ostomy</subject><subject>Pediatric Surgery</subject><subject>Pediatrics</subject><subject>Picibanil - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Sclerotherapy</subject><subject>Sclerotherapy - methods</subject><subject>Sirolimus - therapeutic use</subject><subject>Surgery</subject><subject>Tracheostomy</subject><subject>Tracheotomy</subject><subject>Treatment Outcome</subject><issn>0179-0358</issn><issn>1437-9813</issn><issn>1437-9813</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkcFu1DAQhi0EotvCC3BAlrhwCYzjJLaPqCpQqYgLnC2vPdl15TjBdkB5Bx4ab7cIidOMZj79mvl_Ql4xeMcAxPsMwCVvoO0a6FUnmu0J2bGOi0ZJxp-SHTChGuC9vCCXOd8DgOSDek4uuBqUGjjfkd9f1lC889n6Jfho0kbLEZNZcC3e0lySKXjY6C9fjtQsS5qX5OuIFj_5eKAmOjrNzgRfPGY6zomWhKacdhbTT2_n0VhvAg3btBzNSXQyoXJT7eeYqY_UHn1wCeML8mw0IePLx3pFvn-8-Xb9ubn7-un2-sNds7BWbs3gWmcZtD1DyfYj9G7PHUc-9h3WWY_7QUhreoGibQfFRgfCCjkKyTplJPAr8vasW9_5sWIueqoGYAgm4rxmzVknGO8G6Cv65j_0fl5TrNc9UK0UIIZKvX6k1v2ETlePpmql_utzBfgZyHUVD5j-yTDQpzT1OU1d09QPaeqN_wHADpQe</recordid><startdate>20241219</startdate><enddate>20241219</enddate><creator>Suzuki, Kento</creator><creator>Fumino, Shigehisa</creator><creator>Iguchi, Masafumi</creator><creator>Takayama, Shohei</creator><creator>Kim, Kiyokazu</creator><creator>Hirano, Shigeru</creator><creator>Ono, Shigeru</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20241219</creationdate><title>Multidisciplinary therapeutic strategy with appropriate timing and modalities for treating cervicofacial lymphatic malformations in children</title><author>Suzuki, Kento ; Fumino, Shigehisa ; Iguchi, Masafumi ; Takayama, Shohei ; Kim, Kiyokazu ; Hirano, Shigeru ; Ono, Shigeru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p128y-6d2dc10251e81bf05db3d3e3f54e51e5eb678ca57e722691fd07c78f78149a803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Combined Modality Therapy</topic><topic>Face - abnormalities</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Lymphatic Abnormalities - therapy</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neck - abnormalities</topic><topic>Original Article</topic><topic>Ostomy</topic><topic>Pediatric Surgery</topic><topic>Pediatrics</topic><topic>Picibanil - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Sclerotherapy</topic><topic>Sclerotherapy - methods</topic><topic>Sirolimus - therapeutic use</topic><topic>Surgery</topic><topic>Tracheostomy</topic><topic>Tracheotomy</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suzuki, Kento</creatorcontrib><creatorcontrib>Fumino, Shigehisa</creatorcontrib><creatorcontrib>Iguchi, Masafumi</creatorcontrib><creatorcontrib>Takayama, Shohei</creatorcontrib><creatorcontrib>Kim, Kiyokazu</creatorcontrib><creatorcontrib>Hirano, Shigeru</creatorcontrib><creatorcontrib>Ono, Shigeru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric surgery international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, Kento</au><au>Fumino, Shigehisa</au><au>Iguchi, Masafumi</au><au>Takayama, Shohei</au><au>Kim, Kiyokazu</au><au>Hirano, Shigeru</au><au>Ono, Shigeru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multidisciplinary therapeutic strategy with appropriate timing and modalities for treating cervicofacial lymphatic malformations in children</atitle><jtitle>Pediatric surgery international</jtitle><stitle>Pediatr Surg Int</stitle><addtitle>Pediatr Surg Int</addtitle><date>2024-12-19</date><risdate>2024</risdate><volume>41</volume><issue>1</issue><spage>35</spage><pages>35-</pages><issn>0179-0358</issn><issn>1437-9813</issn><eissn>1437-9813</eissn><abstract>Purpose
The study reviewed a multidisciplinary approach to treating cervicofacial lymphatic malformations (CFLMs) in children.
Methods
Between 2007 and 2023, 53 children with CFLMs were treated with the median on-set age of 5 months (0–165) at our institute. For infants, airway management, including possible tracheotomy was prioritized, and a “wait-and-see” policy was adopted to expect spontaneous regression. Once children reached one year of age or diagnosed after infancy, OK-432 sclerotherapy and surgical treatment with/without sirolimus were considered for residual lesions.
Results
The median follow-up period was 38 months (0–169). Among 30 infants, tracheostomy was performed in 4 patients, with 3 successfully closed after treatment. Thirteen patients showed excellent improvement without treatment. Sclerotherapy was performed in 15 patients, and partial resection in 5. Six patients were treated with sirolimus and showed moderate shrinkage or cessation of bleeding. Overall, 23 of 30 infants showed moderate to excellent improvement. For the 23 patients diagnosed after infancy, 16 improved without treatment, and 7 showed moderate to excellent improvement with sclerotherapy.
Conclusions
The study concluded that early sclerotherapy for infants, particularly around the airway, poses risks, and tracheostomy might be necessary. The comprehensive strategy including "wait-and-see," sclerotherapy, sirolimus treatment, and timely surgery significantly improved the patients' quality of life.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>39699633</pmid><doi>10.1007/s00383-024-05947-y</doi></addata></record> |
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subjects | Adolescent Child Child, Preschool Combined Modality Therapy Face - abnormalities Female Follow-Up Studies Humans Infant Infant, Newborn Lymphatic Abnormalities - therapy Male Medicine Medicine & Public Health Neck - abnormalities Original Article Ostomy Pediatric Surgery Pediatrics Picibanil - therapeutic use Retrospective Studies Sclerotherapy Sclerotherapy - methods Sirolimus - therapeutic use Surgery Tracheostomy Tracheotomy Treatment Outcome |
title | Multidisciplinary therapeutic strategy with appropriate timing and modalities for treating cervicofacial lymphatic malformations in children |
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