LymphedemaV1, PubMed, Checkpoint, bibRecord, 008069

[Generalized lymphatic dysplasia in a 6-month-old nursing infant].

Identifieur interne : 008069 ( PubMed/Checkpoint ); précédent : 008068; suivant : 008070

[Generalized lymphatic dysplasia in a 6-month-old nursing infant].

Auteurs : L. Massimo [Italie] ; G. Di Iorio ; A. Martone ; R. Sottile ; A. Retolatto ; F. Loiodice ; A. Campa ; S. Angelone

Source :

La Pediatria medica e chirurgica : Medical and surgical pediatrics [ 0391-5387 ]

RBID : pubmed:2052465

Descripteurs français

KwdFr :
- Ascite chyleuse (), Ascite chyleuse (diagnostic), Association thérapeutique (), Chylothorax (), Chylothorax (diagnostic), Humains, Lymphoedème (), Lymphoedème (diagnostic), Maladies lymphatiques (), Maladies lymphatiques (diagnostic), Mâle, Nourrisson, Syndrome.
MESH :
- diagnostic : Ascite chyleuse, Chylothorax, Lymphoedème, Maladies lymphatiques.
- Ascite chyleuse, Association thérapeutique, Chylothorax, Humains, Lymphoedème, Maladies lymphatiques, Mâle, Nourrisson, Syndrome.

English descriptors

KwdEn :
- Chylothorax (diagnosis), Chylothorax (therapy), Chylous Ascites (diagnosis), Chylous Ascites (therapy), Combined Modality Therapy (methods), Humans, Infant, Lymphatic Diseases (diagnosis), Lymphatic Diseases (therapy), Lymphedema (diagnosis), Lymphedema (therapy), Male, Syndrome.
MESH :
- diagnosis : Chylothorax, Chylous Ascites, Lymphatic Diseases, Lymphedema.
- methods : Combined Modality Therapy.
- therapy : Chylothorax, Chylous Ascites, Lymphatic Diseases, Lymphedema.
- Humans, Infant, Male, Syndrome.

Abstract

G.L.D. is a rare syndrome characterized by chylothorax, chylous ascites and lymphedema associated to minor symptoms following from lymphangiectasis or to lymphangiomatosis. This syndrome is caused by congenital dysplasia of lymphatic vessels and has, generally, an extremely severe prognosis. In the present papers the authors describe one case of G.L.D. in a six months old infant with chylous ascites, chylothorax, lymphedema, hemangioma and a history of fetal ascites. The preservative (dietetic and evacuative) therapy was not resolutive, therefore an exploratory laparotomy was necessary, but no surgical solution was possible because of the absence of chylous vessels in the anatomical region of the principal lymphatic route. However, laparatomy led to a progressive recovery of ascites and chylothorax, probably due to thrombosis of dysplasic lymph vessels and to neoformation of collateral circulation.

PubMed: 2052465

Affiliations:

Italie

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pubmed:2052465

Le document en format XML

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<author><name sortKey="Massimo, L" sort="Massimo, L" uniqKey="Massimo L" first="L" last="Massimo">L. Massimo</name>
<affiliation wicri:level="1"><nlm:affiliation>I Divisione di Pediatria, Ospedale Santobono, USL 40 Napoli, Italia.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>I Divisione di Pediatria, Ospedale Santobono, USL 40 Napoli</wicri:regionArea>
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<author><name sortKey="Martone, A" sort="Martone, A" uniqKey="Martone A" first="A" last="Martone">A. Martone</name>
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<author><name sortKey="Sottile, R" sort="Sottile, R" uniqKey="Sottile R" first="R" last="Sottile">R. Sottile</name>
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<author><name sortKey="Retolatto, A" sort="Retolatto, A" uniqKey="Retolatto A" first="A" last="Retolatto">A. Retolatto</name>
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<author><name sortKey="Loiodice, F" sort="Loiodice, F" uniqKey="Loiodice F" first="F" last="Loiodice">F. Loiodice</name>
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<author><name sortKey="Campa, A" sort="Campa, A" uniqKey="Campa A" first="A" last="Campa">A. Campa</name>
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<author><name sortKey="Angelone, S" sort="Angelone, S" uniqKey="Angelone S" first="S" last="Angelone">S. Angelone</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chylothorax (diagnosis)</term>
<term>Chylothorax (therapy)</term>
<term>Chylous Ascites (diagnosis)</term>
<term>Chylous Ascites (therapy)</term>
<term>Combined Modality Therapy (methods)</term>
<term>Humans</term>
<term>Infant</term>
<term>Lymphatic Diseases (diagnosis)</term>
<term>Lymphatic Diseases (therapy)</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (therapy)</term>
<term>Male</term>
<term>Syndrome</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Ascite chyleuse ()</term>
<term>Ascite chyleuse (diagnostic)</term>
<term>Association thérapeutique ()</term>
<term>Chylothorax ()</term>
<term>Chylothorax (diagnostic)</term>
<term>Humains</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (diagnostic)</term>
<term>Maladies lymphatiques ()</term>
<term>Maladies lymphatiques (diagnostic)</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Chylothorax</term>
<term>Chylous Ascites</term>
<term>Lymphatic Diseases</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Ascite chyleuse</term>
<term>Chylothorax</term>
<term>Lymphoedème</term>
<term>Maladies lymphatiques</term>
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<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Combined Modality Therapy</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Chylothorax</term>
<term>Chylous Ascites</term>
<term>Lymphatic Diseases</term>
<term>Lymphedema</term>
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<keywords scheme="MESH" xml:lang="en"><term>Humans</term>
<term>Infant</term>
<term>Male</term>
<term>Syndrome</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Ascite chyleuse</term>
<term>Association thérapeutique</term>
<term>Chylothorax</term>
<term>Humains</term>
<term>Lymphoedème</term>
<term>Maladies lymphatiques</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Syndrome</term>
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<front><div type="abstract" xml:lang="en">G.L.D. is a rare syndrome characterized by chylothorax, chylous ascites and lymphedema associated to minor symptoms following from lymphangiectasis or to lymphangiomatosis. This syndrome is caused by congenital dysplasia of lymphatic vessels and has, generally, an extremely severe prognosis. In the present papers the authors describe one case of G.L.D. in a six months old infant with chylous ascites, chylothorax, lymphedema, hemangioma and a history of fetal ascites. The preservative (dietetic and evacuative) therapy was not resolutive, therefore an exploratory laparotomy was necessary, but no surgical solution was possible because of the absence of chylous vessels in the anatomical region of the principal lymphatic route. However, laparatomy led to a progressive recovery of ascites and chylothorax, probably due to thrombosis of dysplasic lymph vessels and to neoformation of collateral circulation.</div>
</front>
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<DateCreated><Year>1991</Year>
<Month>07</Month>
<Day>24</Day>
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<DateRevised><Year>2006</Year>
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<Title>La Pediatria medica e chirurgica : Medical and surgical pediatrics</Title>
<ISOAbbreviation>Pediatr Med Chir</ISOAbbreviation>
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<ArticleTitle>[Generalized lymphatic dysplasia in a 6-month-old nursing infant].</ArticleTitle>
<Pagination><MedlinePgn>99-103</MedlinePgn>
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<Abstract><AbstractText>G.L.D. is a rare syndrome characterized by chylothorax, chylous ascites and lymphedema associated to minor symptoms following from lymphangiectasis or to lymphangiomatosis. This syndrome is caused by congenital dysplasia of lymphatic vessels and has, generally, an extremely severe prognosis. In the present papers the authors describe one case of G.L.D. in a six months old infant with chylous ascites, chylothorax, lymphedema, hemangioma and a history of fetal ascites. The preservative (dietetic and evacuative) therapy was not resolutive, therefore an exploratory laparotomy was necessary, but no surgical solution was possible because of the absence of chylous vessels in the anatomical region of the principal lymphatic route. However, laparatomy led to a progressive recovery of ascites and chylothorax, probably due to thrombosis of dysplasic lymph vessels and to neoformation of collateral circulation.</AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Massimo</LastName>
<ForeName>L</ForeName>
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<AffiliationInfo><Affiliation>I Divisione di Pediatria, Ospedale Santobono, USL 40 Napoli, Italia.</Affiliation>
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<Author ValidYN="Y"><LastName>Di Iorio</LastName>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D002916" MajorTopicYN="N">Chylothorax</DescriptorName>
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<tree><noCountry><name sortKey="Angelone, S" sort="Angelone, S" uniqKey="Angelone S" first="S" last="Angelone">S. Angelone</name>
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<name sortKey="Di Iorio, G" sort="Di Iorio, G" uniqKey="Di Iorio G" first="G" last="Di Iorio">G. Di Iorio</name>
<name sortKey="Loiodice, F" sort="Loiodice, F" uniqKey="Loiodice F" first="F" last="Loiodice">F. Loiodice</name>
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<name sortKey="Sottile, R" sort="Sottile, R" uniqKey="Sottile R" first="R" last="Sottile">R. Sottile</name>
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<country name="Italie"><noRegion><name sortKey="Massimo, L" sort="Massimo, L" uniqKey="Massimo L" first="L" last="Massimo">L. Massimo</name>
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[Generalized lymphatic dysplasia in a 6-month-old nursing infant].

[Generalized lymphatic dysplasia in a 6-month-old nursing infant].

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki