[Primary congenital lymphedema: Milroy disease: the first case observed in the Department of Pediatrics at the University Hospital Yalgado Ouedraogo, Ouagadougou].
Identifieur interne : 000085 ( PubMed/Curation ); précédent : 000084; suivant : 000086[Primary congenital lymphedema: Milroy disease: the first case observed in the Department of Pediatrics at the University Hospital Yalgado Ouedraogo, Ouagadougou].
Auteurs : Chantal Zoungrana Ouattara [Burkina Faso] ; Angèle Kalmogho [Burkina Faso] ; Caroline Yonaba [Burkina Faso] ; Chantal Gabrielle Bouda [Burkina Faso] ; Ghislaine Yaméogo [Burkina Faso] ; Ludovic Kam [Burkina Faso]Source :
- The Pan African medical journal [ 1937-8688 ] ; 2017.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Lymphoedème.
- étiologie : Érysipèle.
- Bandages, Bas de contention, Burkina, Enfant, Femelle, Humains, Hôpitaux universitaires, Lymphoedème, Psychothérapie, Techniques de physiothérapie.
English descriptors
- KwdEn :
- MESH :
- congenital : Lymphedema.
- diagnosis : Lymphedema.
- etiology : Erysipelas.
- methods : Psychotherapy.
- therapy : Lymphedema.
- Bandages, Burkina Faso, Child, Female, Hospitals, University, Humans, Physical Therapy Modalities, Stockings, Compression.
Abstract
Congenital lymphedema is the accumulation of lymphatic fluid in the child's interstitial spaces. Milroy disease is a rare, hereditary, autosomal dominant condition showing incomplete penetrance. We report the case of a 7-year old little girl with Milroy disease examined for erysipelas on congenital big right leg. A family history of large congenital member existed. Physical examination showed big oedematous right leg painful to palpation, with skin lichenification and erysipelas. Paraclinical assessment objectified cutaneous lymphedema with vascular involvement suggestive of ectasia of the right saphenous vein. Female karyotype showed no abnormalities, despite the small chromosomal rearrangements. Treatment was based on physiotherapy, bandages, compression stockings and psychotherapy. This first case in Burkina Faso testifies to the rarity of the pathology but especially to the diagnostic difficulties related to the inadequacy of paraclinical investigations.
DOI: 10.11604/pamj.2017.27.21.11443
PubMed: 28748022
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Chantal Zoungrana" uniqKey="Ouattara C" first="Chantal Zoungrana" last="Ouattara">Chantal Zoungrana Ouattara</name><affiliation wicri:level="1"><nlm:affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</nlm:affiliation><country xml:lang="fr" wicri:curation="lc">Burkina Faso</country><wicri:regionArea>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou</wicri:regionArea></affiliation></author><author><name sortKey="Kalmogho, Angele" sort="Kalmogho, Angele" uniqKey="Kalmogho A" first="Angèle" last="Kalmogho">Angèle Kalmogho</name><affiliation wicri:level="1"><nlm:affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</nlm:affiliation><country xml:lang="fr" wicri:curation="lc">Burkina Faso</country><wicri:regionArea>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou</wicri:regionArea></affiliation></author><author><name sortKey="Yonaba, Caroline" sort="Yonaba, Caroline" uniqKey="Yonaba C" first="Caroline" last="Yonaba">Caroline Yonaba</name><affiliation wicri:level="1"><nlm:affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</nlm:affiliation><country xml:lang="fr" wicri:curation="lc">Burkina Faso</country><wicri:regionArea>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou</wicri:regionArea></affiliation></author><author><name sortKey="Bouda, Chantal Gabrielle" sort="Bouda, Chantal Gabrielle" uniqKey="Bouda C" first="Chantal Gabrielle" last="Bouda">Chantal Gabrielle Bouda</name><affiliation wicri:level="1"><nlm:affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</nlm:affiliation><country xml:lang="fr" wicri:curation="lc">Burkina Faso</country><wicri:regionArea>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou</wicri:regionArea></affiliation></author><author><name sortKey="Yameogo, Ghislaine" sort="Yameogo, Ghislaine" uniqKey="Yameogo G" first="Ghislaine" last="Yaméogo">Ghislaine Yaméogo</name><affiliation wicri:level="1"><nlm:affiliation>Service de Pédiatrie Médicale du CHU Charles de Gaulle de Ouagadougou, Burkina-faso.</nlm:affiliation><country xml:lang="fr" wicri:curation="lc">Burkina Faso</country><wicri:regionArea>Service de Pédiatrie Médicale du CHU Charles de Gaulle de Ouagadougou</wicri:regionArea></affiliation></author><author><name sortKey="Kam, Ludovic" sort="Kam, Ludovic" uniqKey="Kam L" first="Ludovic" last="Kam">Ludovic Kam</name><affiliation wicri:level="1"><nlm:affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</nlm:affiliation><country xml:lang="fr" wicri:curation="lc">Burkina Faso</country><wicri:regionArea>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou</wicri:regionArea></affiliation></author></analytic><series><title level="j">The Pan African medical journal</title><idno type="eISSN">1937-8688</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bandages</term><term>Burkina Faso</term><term>Child</term><term>Erysipelas (etiology)</term><term>Female</term><term>Hospitals, University</term><term>Humans</term><term>Lymphedema (congenital)</term><term>Lymphedema (diagnosis)</term><term>Lymphedema (therapy)</term><term>Physical Therapy Modalities</term><term>Psychotherapy (methods)</term><term>Stockings, Compression</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Bandages</term><term>Bas de contention</term><term>Burkina</term><term>Enfant</term><term>Femelle</term><term>Humains</term><term>Hôpitaux universitaires</term><term>Lymphoedème ()</term><term>Lymphoedème (diagnostic)</term><term>Psychothérapie ()</term><term>Techniques de physiothérapie</term><term>Érysipèle (étiologie)</term></keywords><keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Lymphoedème</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Erysipelas</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Psychotherapy</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="étiologie" xml:lang="fr"><term>Érysipèle</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Bandages</term><term>Burkina Faso</term><term>Child</term><term>Female</term><term>Hospitals, University</term><term>Humans</term><term>Physical Therapy Modalities</term><term>Stockings, Compression</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Bandages</term><term>Bas de contention</term><term>Burkina</term><term>Enfant</term><term>Femelle</term><term>Humains</term><term>Hôpitaux universitaires</term><term>Lymphoedème</term><term>Psychothérapie</term><term>Techniques de physiothérapie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Congenital lymphedema is the accumulation of lymphatic fluid in the child's interstitial spaces. Milroy disease is a rare, hereditary, autosomal dominant condition showing incomplete penetrance. We report the case of a 7-year old little girl with Milroy disease examined for erysipelas on congenital big right leg. A family history of large congenital member existed. Physical examination showed big oedematous right leg painful to palpation, with skin lichenification and erysipelas. Paraclinical assessment objectified cutaneous lymphedema with vascular involvement suggestive of ectasia of the right saphenous vein. Female karyotype showed no abnormalities, despite the small chromosomal rearrangements. Treatment was based on physiotherapy, bandages, compression stockings and psychotherapy. This first case in Burkina Faso testifies to the rarity of the pathology but especially to the diagnostic difficulties related to the inadequacy of paraclinical investigations.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">28748022</PMID><DateCreated><Year>2017</Year><Month>07</Month><Day>27</Day></DateCreated><DateCompleted><Year>2017</Year><Month>08</Month><Day>04</Day></DateCompleted><DateRevised><Year>2017</Year><Month>08</Month><Day>04</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Electronic">1937-8688</ISSN><JournalIssue CitedMedium="Internet"><Volume>27</Volume><PubDate><Year>2017</Year></PubDate></JournalIssue><Title>The Pan African medical journal</Title><ISOAbbreviation>Pan Afr Med J</ISOAbbreviation></Journal><ArticleTitle>[Primary congenital lymphedema: Milroy disease: the first case observed in the Department of Pediatrics at the University Hospital Yalgado Ouedraogo, Ouagadougou].</ArticleTitle><Pagination><MedlinePgn>21</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.11604/pamj.2017.27.21.11443</ELocationID><Abstract><AbstractText>Congenital lymphedema is the accumulation of lymphatic fluid in the child's interstitial spaces. Milroy disease is a rare, hereditary, autosomal dominant condition showing incomplete penetrance. We report the case of a 7-year old little girl with Milroy disease examined for erysipelas on congenital big right leg. A family history of large congenital member existed. Physical examination showed big oedematous right leg painful to palpation, with skin lichenification and erysipelas. Paraclinical assessment objectified cutaneous lymphedema with vascular involvement suggestive of ectasia of the right saphenous vein. Female karyotype showed no abnormalities, despite the small chromosomal rearrangements. Treatment was based on physiotherapy, bandages, compression stockings and psychotherapy. This first case in Burkina Faso testifies to the rarity of the pathology but especially to the diagnostic difficulties related to the inadequacy of paraclinical investigations.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ouattara</LastName><ForeName>Chantal Zoungrana</ForeName><Initials>CZ</Initials><AffiliationInfo><Affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Unité de Formation et de Recherche en Sciences de la Santé (UFR/SDS), Université de Ouagadougou, Burkina Faso.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kalmogho</LastName><ForeName>Angèle</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Unité de Formation et de Recherche en Sciences de la Santé (UFR/SDS), Université de Ouagadougou, Burkina Faso.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yonaba</LastName><ForeName>Caroline</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Unité de Formation et de Recherche en Sciences de la Santé (UFR/SDS), Université de Ouagadougou, Burkina Faso.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Bouda</LastName><ForeName>Chantal Gabrielle</ForeName><Initials>CG</Initials><AffiliationInfo><Affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yaméogo</LastName><ForeName>Ghislaine</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Service de Pédiatrie Médicale du CHU Charles de Gaulle de Ouagadougou, Burkina-faso.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kam</LastName><ForeName>Ludovic</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Département de Pédiatrie du CHU Yalgado Ouédraogo de Ouagadougou, Burkina-faso.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Unité de Formation et de Recherche en Sciences de la Santé (UFR/SDS), Université de Ouagadougou, Burkina Faso.</Affiliation></AffiliationInfo></Author></AuthorList><Language>fre</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><VernacularTitle>Le lymphœdème congénital primaire: la maladie de Milroy: à propos du premier cas observé dans le Département de Pédiatrie du Centre Hospitalier Universitaire Yalgado Ouédraogo, Ouagadougou.</VernacularTitle><ArticleDate DateType="Electronic"><Year>2017</Year><Month>05</Month><Day>09</Day></ArticleDate></Article><MedlineJournalInfo><Country>Uganda</Country><MedlineTA>Pan Afr Med J</MedlineTA><NlmUniqueID>101517926</NlmUniqueID></MedlineJournalInfo><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Rev Med Interne. 2012 May;33(5):268-72</RefSource><PMID Version="1">22296831</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Clin Genet. 2007 Feb;71(2):187-9</RefSource><PMID Version="1">17250670</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Pediatrics. 1985 Aug;76(2):206-18</RefSource><PMID Version="1">4022694</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Mal Vasc. 2003 Dec;28(5):269-76</RefSource><PMID Version="1">14978432</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Pan Afr Med J. 2014 Nov 21;19:311</RefSource><PMID Version="1">25883738</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Pediatr. 2009 Jul;155(1):90-3</RefSource><PMID Version="1">19394045</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>In Vivo. 2010 May-Jun;24(3):309-14</RefSource><PMID Version="1">20555004</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Ann Dermatol Venereol. 2012 Nov;139(11):744-50; quiz 751-2</RefSource><PMID Version="1">23199775</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Mal Vasc. 2009 Nov;34(5):314-22</RefSource><PMID Version="1">20050179</PMID></CommentsCorrections></CommentsCorrectionsList><MeshHeadingList><MeshHeading><DescriptorName UI="D001458" MajorTopicYN="N">Bandages</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002050" MajorTopicYN="N">Burkina Faso</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004886" MajorTopicYN="N">Erysipelas</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006785" MajorTopicYN="N">Hospitals, University</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000151" MajorTopicYN="N">congenital</QualifierName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D026741" MajorTopicYN="Y">Physical Therapy Modalities</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011613" MajorTopicYN="N">Psychotherapy</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D053828" MajorTopicYN="N">Stockings, Compression</DescriptorName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Milroy disease</Keyword><Keyword MajorTopicYN="N">Ouagadougou</Keyword><Keyword MajorTopicYN="N">Primary lymphedema</Keyword><Keyword MajorTopicYN="N">diagnosis</Keyword><Keyword MajorTopicYN="N">treatment</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2016</Year><Month>12</Month><Day>18</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2017</Year><Month>04</Month><Day>10</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2017</Year><Month>7</Month><Day>28</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2017</Year><Month>7</Month><Day>28</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2017</Year><Month>8</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">28748022</ArticleId><ArticleId IdType="doi">10.11604/pamj.2017.27.21.11443</ArticleId><ArticleId IdType="pii">PAMJ-27-21</ArticleId><ArticleId IdType="pmc">PMC5511709</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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