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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Veröffentlicht in:Pediatric surgery international 2024-12, Vol.41 (1), p.35
Hauptverfasser: Suzuki, Kento, Fumino, Shigehisa, Iguchi, Masafumi, Takayama, Shohei, Kim, Kiyokazu, Hirano, Shigeru, Ono, Shigeru
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container_issue 1
container_start_page 35
container_title Pediatric surgery international
container_volume 41
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
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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 &amp; 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. 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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. 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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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