Loading…

CLINICAL IMPROVEMENT OF DIFFUSE LYMPHANGIOMATOSIS WITH PEGYLATED INTERFERON ALFA-2B THERAPY: Case Report and Review of the Literature

Diffuse lymphangiomatosis is a very rare congenital disease, characterized by diffuse or multifocal lymphangioma in the skeletal tissue, spleen, liver, mediastinum, and/or lung. The prognosis is usually poor, especially for children with thoracic lesion, and treatments for the disease are controvers...

Full description

Saved in:
Bibliographic Details
Published in:Pediatric hematology and oncology 2007-01, Vol.24 (7), p.513-524
Main Authors: Ozeki, Michio, Funato, Michinori, Kanda, Kaori, Ito, Masahumi, Teramoto, Takahide, Kaneko, Hideo, Fukao, Toshiyuki, Kondo, Naomi
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c404t-f621b56869b0e2ee08d1a91b8c6d0d310f8a7eff4d79be42e288e9a8b415b503
cites cdi_FETCH-LOGICAL-c404t-f621b56869b0e2ee08d1a91b8c6d0d310f8a7eff4d79be42e288e9a8b415b503
container_end_page 524
container_issue 7
container_start_page 513
container_title Pediatric hematology and oncology
container_volume 24
creator Ozeki, Michio
Funato, Michinori
Kanda, Kaori
Ito, Masahumi
Teramoto, Takahide
Kaneko, Hideo
Fukao, Toshiyuki
Kondo, Naomi
description Diffuse lymphangiomatosis is a very rare congenital disease, characterized by diffuse or multifocal lymphangioma in the skeletal tissue, spleen, liver, mediastinum, and/or lung. The prognosis is usually poor, especially for children with thoracic lesion, and treatments for the disease are controversial. The authors report a 9-year-old boy with diffuse lymphangiomatosis involving the thorax with pleural effusions, the spleen, and systemic bone. The patient was treated with pegylated interferon alfa-2b, and achieved good clinical and radiological improvement.
doi_str_mv 10.1080/08880010701533603
format article
fullrecord <record><control><sourceid>proquest_infor</sourceid><recordid>TN_cdi_informaworld_taylorfrancis_310_1080_08880010701533603</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68241406</sourcerecordid><originalsourceid>FETCH-LOGICAL-c404t-f621b56869b0e2ee08d1a91b8c6d0d310f8a7eff4d79be42e288e9a8b415b503</originalsourceid><addsrcrecordid>eNp9kF2Pk0AUhidG49bVH-CNmSvv0DN8DIN6g11oSSg0FDW9IgMcUjYU6gy42R_g_5amTYwx2atzkvO8b04eQt4y-MBAwEcQQgAwcIE5lsXBekYWzDGZAZx7z8nifDdmQNyQV1rfA4BpueZLcsNcV3BXuAvyexlHSbT0Yxpttln6PdgESU7TkN5FYfhtF9B4v9mu_WQVpRs_T3fRjv6I8jXdBqt97OfBHY2SPMjCIEsT6sehb5hfab4OMn-7_0SXUiPN8DSokcq-ntdfLT7QoaHjAWncjqjkOCl8TV40stP45jpvSR4G-XJtxOnq_JxR2WCPRsNNVjpccK8ENBFB1Ex6rBQVr6G2GDRCutg0du16JdommkKgJ0VpM6d0wLol7y-1JzX8nFCPxbHVFXad7HGYdMGFaTMb-AyyC1ipQWuFTXFS7VGqx4JBcVZf_Kd-zry7lk_lEeu_iavrGfhyAdq-GdRRPgyqq4tRPnaDapTsq1YX1lP9n_-JH1B246GSCov7YVL97O2J7_4AwFackA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68241406</pqid></control><display><type>article</type><title>CLINICAL IMPROVEMENT OF DIFFUSE LYMPHANGIOMATOSIS WITH PEGYLATED INTERFERON ALFA-2B THERAPY: Case Report and Review of the Literature</title><source>Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)</source><creator>Ozeki, Michio ; Funato, Michinori ; Kanda, Kaori ; Ito, Masahumi ; Teramoto, Takahide ; Kaneko, Hideo ; Fukao, Toshiyuki ; Kondo, Naomi</creator><creatorcontrib>Ozeki, Michio ; Funato, Michinori ; Kanda, Kaori ; Ito, Masahumi ; Teramoto, Takahide ; Kaneko, Hideo ; Fukao, Toshiyuki ; Kondo, Naomi</creatorcontrib><description>Diffuse lymphangiomatosis is a very rare congenital disease, characterized by diffuse or multifocal lymphangioma in the skeletal tissue, spleen, liver, mediastinum, and/or lung. The prognosis is usually poor, especially for children with thoracic lesion, and treatments for the disease are controversial. The authors report a 9-year-old boy with diffuse lymphangiomatosis involving the thorax with pleural effusions, the spleen, and systemic bone. The patient was treated with pegylated interferon alfa-2b, and achieved good clinical and radiological improvement.</description><identifier>ISSN: 0888-0018</identifier><identifier>EISSN: 1521-0669</identifier><identifier>DOI: 10.1080/08880010701533603</identifier><identifier>PMID: 17786787</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Child ; D2-40 ; diffuse lymphangiomatosis ; Humans ; Interferon-alpha - administration &amp; dosage ; Interferon-alpha - blood ; Interferon-alpha - therapeutic use ; Lymphangioma - diagnostic imaging ; Lymphangioma - drug therapy ; Lymphangioma - physiopathology ; Male ; pegylated interferon alfa-2b ; pleural effusion ; Polyethylene Glycols ; Radiography ; Recombinant Proteins ; vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - metabolism</subject><ispartof>Pediatric hematology and oncology, 2007-01, Vol.24 (7), p.513-524</ispartof><rights>2007 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-f621b56869b0e2ee08d1a91b8c6d0d310f8a7eff4d79be42e288e9a8b415b503</citedby><cites>FETCH-LOGICAL-c404t-f621b56869b0e2ee08d1a91b8c6d0d310f8a7eff4d79be42e288e9a8b415b503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17786787$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ozeki, Michio</creatorcontrib><creatorcontrib>Funato, Michinori</creatorcontrib><creatorcontrib>Kanda, Kaori</creatorcontrib><creatorcontrib>Ito, Masahumi</creatorcontrib><creatorcontrib>Teramoto, Takahide</creatorcontrib><creatorcontrib>Kaneko, Hideo</creatorcontrib><creatorcontrib>Fukao, Toshiyuki</creatorcontrib><creatorcontrib>Kondo, Naomi</creatorcontrib><title>CLINICAL IMPROVEMENT OF DIFFUSE LYMPHANGIOMATOSIS WITH PEGYLATED INTERFERON ALFA-2B THERAPY: Case Report and Review of the Literature</title><title>Pediatric hematology and oncology</title><addtitle>Pediatr Hematol Oncol</addtitle><description>Diffuse lymphangiomatosis is a very rare congenital disease, characterized by diffuse or multifocal lymphangioma in the skeletal tissue, spleen, liver, mediastinum, and/or lung. The prognosis is usually poor, especially for children with thoracic lesion, and treatments for the disease are controversial. The authors report a 9-year-old boy with diffuse lymphangiomatosis involving the thorax with pleural effusions, the spleen, and systemic bone. The patient was treated with pegylated interferon alfa-2b, and achieved good clinical and radiological improvement.</description><subject>Child</subject><subject>D2-40</subject><subject>diffuse lymphangiomatosis</subject><subject>Humans</subject><subject>Interferon-alpha - administration &amp; dosage</subject><subject>Interferon-alpha - blood</subject><subject>Interferon-alpha - therapeutic use</subject><subject>Lymphangioma - diagnostic imaging</subject><subject>Lymphangioma - drug therapy</subject><subject>Lymphangioma - physiopathology</subject><subject>Male</subject><subject>pegylated interferon alfa-2b</subject><subject>pleural effusion</subject><subject>Polyethylene Glycols</subject><subject>Radiography</subject><subject>Recombinant Proteins</subject><subject>vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>0888-0018</issn><issn>1521-0669</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9kF2Pk0AUhidG49bVH-CNmSvv0DN8DIN6g11oSSg0FDW9IgMcUjYU6gy42R_g_5amTYwx2atzkvO8b04eQt4y-MBAwEcQQgAwcIE5lsXBekYWzDGZAZx7z8nifDdmQNyQV1rfA4BpueZLcsNcV3BXuAvyexlHSbT0Yxpttln6PdgESU7TkN5FYfhtF9B4v9mu_WQVpRs_T3fRjv6I8jXdBqt97OfBHY2SPMjCIEsT6sehb5hfab4OMn-7_0SXUiPN8DSokcq-ntdfLT7QoaHjAWncjqjkOCl8TV40stP45jpvSR4G-XJtxOnq_JxR2WCPRsNNVjpccK8ENBFB1Ex6rBQVr6G2GDRCutg0du16JdommkKgJ0VpM6d0wLol7y-1JzX8nFCPxbHVFXad7HGYdMGFaTMb-AyyC1ipQWuFTXFS7VGqx4JBcVZf_Kd-zry7lk_lEeu_iavrGfhyAdq-GdRRPgyqq4tRPnaDapTsq1YX1lP9n_-JH1B246GSCov7YVL97O2J7_4AwFackA</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Ozeki, Michio</creator><creator>Funato, Michinori</creator><creator>Kanda, Kaori</creator><creator>Ito, Masahumi</creator><creator>Teramoto, Takahide</creator><creator>Kaneko, Hideo</creator><creator>Fukao, Toshiyuki</creator><creator>Kondo, Naomi</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</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>20070101</creationdate><title>CLINICAL IMPROVEMENT OF DIFFUSE LYMPHANGIOMATOSIS WITH PEGYLATED INTERFERON ALFA-2B THERAPY: Case Report and Review of the Literature</title><author>Ozeki, Michio ; Funato, Michinori ; Kanda, Kaori ; Ito, Masahumi ; Teramoto, Takahide ; Kaneko, Hideo ; Fukao, Toshiyuki ; Kondo, Naomi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-f621b56869b0e2ee08d1a91b8c6d0d310f8a7eff4d79be42e288e9a8b415b503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Child</topic><topic>D2-40</topic><topic>diffuse lymphangiomatosis</topic><topic>Humans</topic><topic>Interferon-alpha - administration &amp; dosage</topic><topic>Interferon-alpha - blood</topic><topic>Interferon-alpha - therapeutic use</topic><topic>Lymphangioma - diagnostic imaging</topic><topic>Lymphangioma - drug therapy</topic><topic>Lymphangioma - physiopathology</topic><topic>Male</topic><topic>pegylated interferon alfa-2b</topic><topic>pleural effusion</topic><topic>Polyethylene Glycols</topic><topic>Radiography</topic><topic>Recombinant Proteins</topic><topic>vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ozeki, Michio</creatorcontrib><creatorcontrib>Funato, Michinori</creatorcontrib><creatorcontrib>Kanda, Kaori</creatorcontrib><creatorcontrib>Ito, Masahumi</creatorcontrib><creatorcontrib>Teramoto, Takahide</creatorcontrib><creatorcontrib>Kaneko, Hideo</creatorcontrib><creatorcontrib>Fukao, Toshiyuki</creatorcontrib><creatorcontrib>Kondo, Naomi</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>Pediatric hematology and oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ozeki, Michio</au><au>Funato, Michinori</au><au>Kanda, Kaori</au><au>Ito, Masahumi</au><au>Teramoto, Takahide</au><au>Kaneko, Hideo</au><au>Fukao, Toshiyuki</au><au>Kondo, Naomi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CLINICAL IMPROVEMENT OF DIFFUSE LYMPHANGIOMATOSIS WITH PEGYLATED INTERFERON ALFA-2B THERAPY: Case Report and Review of the Literature</atitle><jtitle>Pediatric hematology and oncology</jtitle><addtitle>Pediatr Hematol Oncol</addtitle><date>2007-01-01</date><risdate>2007</risdate><volume>24</volume><issue>7</issue><spage>513</spage><epage>524</epage><pages>513-524</pages><issn>0888-0018</issn><eissn>1521-0669</eissn><abstract>Diffuse lymphangiomatosis is a very rare congenital disease, characterized by diffuse or multifocal lymphangioma in the skeletal tissue, spleen, liver, mediastinum, and/or lung. The prognosis is usually poor, especially for children with thoracic lesion, and treatments for the disease are controversial. The authors report a 9-year-old boy with diffuse lymphangiomatosis involving the thorax with pleural effusions, the spleen, and systemic bone. The patient was treated with pegylated interferon alfa-2b, and achieved good clinical and radiological improvement.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>17786787</pmid><doi>10.1080/08880010701533603</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0888-0018
ispartof Pediatric hematology and oncology, 2007-01, Vol.24 (7), p.513-524
issn 0888-0018
1521-0669
language eng
recordid cdi_informaworld_taylorfrancis_310_1080_08880010701533603
source Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)
subjects Child
D2-40
diffuse lymphangiomatosis
Humans
Interferon-alpha - administration & dosage
Interferon-alpha - blood
Interferon-alpha - therapeutic use
Lymphangioma - diagnostic imaging
Lymphangioma - drug therapy
Lymphangioma - physiopathology
Male
pegylated interferon alfa-2b
pleural effusion
Polyethylene Glycols
Radiography
Recombinant Proteins
vascular endothelial growth factor
Vascular Endothelial Growth Factor A - metabolism
title CLINICAL IMPROVEMENT OF DIFFUSE LYMPHANGIOMATOSIS WITH PEGYLATED INTERFERON ALFA-2B THERAPY: Case Report and Review of the Literature
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T15%3A07%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CLINICAL%20IMPROVEMENT%20OF%20DIFFUSE%20LYMPHANGIOMATOSIS%20WITH%20PEGYLATED%20INTERFERON%20ALFA-2B%20THERAPY:%20Case%20Report%20and%20Review%20of%20the%20Literature&rft.jtitle=Pediatric%20hematology%20and%20oncology&rft.au=Ozeki,%20Michio&rft.date=2007-01-01&rft.volume=24&rft.issue=7&rft.spage=513&rft.epage=524&rft.pages=513-524&rft.issn=0888-0018&rft.eissn=1521-0669&rft_id=info:doi/10.1080/08880010701533603&rft_dat=%3Cproquest_infor%3E68241406%3C/proquest_infor%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c404t-f621b56869b0e2ee08d1a91b8c6d0d310f8a7eff4d79be42e288e9a8b415b503%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=68241406&rft_id=info:pmid/17786787&rfr_iscdi=true