Warty skin changes, chronic scrotal lymphoedema, and facial dysmorphism
Identifieur interne : 005522 ( Main/Curation ); précédent : 005521; suivant : 005523Warty skin changes, chronic scrotal lymphoedema, and facial dysmorphism
Auteurs : Moritz Felcht [Allemagne] ; Nicola Dikow [Allemagne] ; Matthias Goebeler [Allemagne] ; Philipp Stroebel [Allemagne] ; Nina Booken [Allemagne] ; Urs Vo Merb Umer [Allemagne] ; Kirsten Merx [Allemagne] ; Thomas Henzler [Allemagne] ; Alexander Marx [Allemagne] ; Ute Moog [Allemagne] ; Sergij Goerdt [Allemagne] ; Claus-Detlev Klemke [Allemagne]Source :
- BMJ Case Reports [ 1757-790X ] ; 2010.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Syndrome de Noonan.
- Adulte d'âge moyen, Chyle, Diagnostic différentiel, Humains, Lymphangiectasie, Mâle, Verrues.
English descriptors
- KwdEn :
- MESH :
- congenital : Lymphangiectasis, Warts.
- diagnosis : Noonan Syndrome.
- Chyle, Diagnosis, Differential, Humans, Male, Middle Aged.
Abstract
We present the case of a 49-year-old Caucasian man whose main complaints were wart-like skin changes and scrotal lymphoedema. Furthermore, our patient showed signs of a common hereditary disease: lymphoedema, short stature, webbed neck, low frontal and posterior hairline, downslanting palpebral fissures, pale blue iris, broad nose, flat philtrum, and prominent nasolabial folds. His ears were low set and retroverted with a thick helix. However, no diagnosis was made for 49 years. The interdisciplinary dialogue of various specialists to make the final diagnosis is presented and discussed.
Url:
DOI: 10.1136/bcr.08.2009.2214
PubMed: 22750922
PubMed Central: 3047285
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PMC:3047285Le document en format XML
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<author><name sortKey="Marx, Alexander" sort="Marx, Alexander" uniqKey="Marx A" first="Alexander" last="Marx">Alexander Marx</name>
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<author><name sortKey="Moog, Ute" sort="Moog, Ute" uniqKey="Moog U" first="Ute" last="Moog">Ute Moog</name>
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</nlm:aff>
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<affiliation wicri:level="3"><nlm:aff id="aff1"><addr-line>University Medicine of Mannheim, Department of Dermatology, Venerology and Allergology, Theodor-Kutzer-Ufer 1-3, Mannheim, 68167, Germany</addr-line>
</nlm:aff>
<country xml:lang="fr">Allemagne</country>
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</nlm:aff>
<country xml:lang="fr">Allemagne</country>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chyle</term>
<term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Lymphangiectasis (congenital)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Noonan Syndrome (diagnosis)</term>
<term>Warts (congenital)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Chyle</term>
<term>Diagnostic différentiel</term>
<term>Humains</term>
<term>Lymphangiectasie ()</term>
<term>Mâle</term>
<term>Syndrome de Noonan (diagnostic)</term>
<term>Verrues ()</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphangiectasis</term>
<term>Warts</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Noonan Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Syndrome de Noonan</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Chyle</term>
<term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Chyle</term>
<term>Diagnostic différentiel</term>
<term>Humains</term>
<term>Lymphangiectasie</term>
<term>Mâle</term>
<term>Verrues</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p>We present the case of a 49-year-old Caucasian man whose main complaints were wart-like skin changes and scrotal lymphoedema. Furthermore, our patient showed signs of a common hereditary disease: lymphoedema, short stature, webbed neck, low frontal and posterior hairline, downslanting palpebral fissures, pale blue iris, broad nose, flat philtrum, and prominent nasolabial folds. His ears were low set and retroverted with a thick helix. However, no diagnosis was made for 49 years. The interdisciplinary dialogue of various specialists to make the final diagnosis is presented and discussed.</p>
</div>
</front>
</TEI>
</record>
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