Vil du vite mer om syndromer?
- Acrokeratoelastoidosis
- Adams-Oliver syndrom
- Angelman syndrom
- Ascher syndrom
- Ataxia telangiektasia
- Auriculotemporal syndrom
- Barraquer-Simons syndrom
- Bazex syndrom
- Berardinelli-Seip syndrom
- Birt-Hogg-Dube syndrom
- Bloom syndrom
- Blue rubber bleb syndrom
- Blueberry muffin syndrom
- Brooke-Spiegler syndrom
- Chediak-Higashi syndrom
- CHILD syndrom
- Clouston syndrom
- Costello syndrom
- Cowden syndrom
- Degos sykdom
- Ehler-Danlos syndrom
- Ektodermale dysplasier
- Fabry sykdom
- Fokal dermal hypoplasi
- Gardner syndrom
- Gorlin syndrom
- Hay-Wells syndrom
- Howell-Evans syndrom
- Huriez syndrom
- Hypereosinofile syndromer
- Hypohidrotisk ektodermal dysplasi
- Hypomelanose av Ito
- Incontinentia pigmenti
- Keratosis follikularis spinulosa dekalvans
- Kindler syndrom
- Klippel-Trénaunay syndrom
- Kobberling-Dunningan syndrom
- Laugier Hunziker syndrom
- LEOPARD syndrom
- Lesch-Nyhan syndrom
- Linear and whorled nevoid hypermelanosis
- Macrocephaly-capillary malformation
- Marfan syndrom
- McCune-Albright syndrom
- McKusick syndrom
- Melkersson-Rosenthal syndrom
- Menke’s syndrom
- Muckle-Wells syndrom
- Muir torre syndrom
- Nail-Patella syndrom
- Naxos sykdom
- Netherton syndrom
- Olmsted’s syndrom
- Pachonychia congenita
- PAPA syndrom
- Papillon-Lefevre syndrom
- Parington kutan amyloidose
- Parry-Romberg syndrom
- Peutz-Jeghers syndrom
- POEMS syndrom
- Progeria
- Proteus syndrom
- Pseudoxantoma elastikum
- Punktat palmoplantar keratodermi
- Reed syndrom
- Reticulate acropigmentation of Kitamura
- Richner-Hanhart syndrom
- Rothmund Thomson syndrom
- SAPHO syndrom
- Schnitzler syndrom
- Sjögren-Larsson syndrom
- Trigeminal trofisk syndrom
- Trousseau syndrom
- Turner syndrom
- Vohlwinkel’s syndrom
- Witkop syndrom
- X-Linked Dominant Chondrodysplasia Punctata
- Xeroderma pigmentosus
- Yellow nail syndrom
- Zinsser-Engman-Cole syndrom
- Acrokeratoelastoidosis
- Adams-Oliver syndrom
- Angelman syndrom
- Ascher syndrom
- Ataxia telangiektasia
- Auriculotemporal syndrom
- Barraquer-Simons syndrom
- Bazex syndrom
- Berardinelli-Seip syndrom
- Birt-Hogg-Dube syndrom
- Bloom syndrom
- Blue rubber bleb syndrom
- Blueberry muffin syndrom
- Brooke-Spiegler syndrom
- Chediak-Higashi syndrom
- CHILD syndrom
- Clouston syndrom
- Costello syndrom
- Cowden syndrom
- Degos sykdom
- Ehler-Danlos syndrom
- Ektodermale dysplasier
- Fabry sykdom
- Fokal dermal hypoplasi
- Gardner syndrom
- Gorlin syndrom
- Hay-Wells syndrom
- Howell-Evans syndrom
- Huriez syndrom
- Hypereosinofile syndromer
- Hypohidrotisk ektodermal dysplasi
- Hypomelanose av Ito
- Incontinentia pigmenti
- Keratosis follikularis spinulosa dekalvans
- Kindler syndrom
- Klippel-Trénaunay syndrom
- Kobberling-Dunningan syndrom
- Laugier Hunziker syndrom
- LEOPARD syndrom
- Lesch-Nyhan syndrom
- Linear and whorled nevoid hypermelanosis
- Macrocephaly-capillary malformation
- Marfan syndrom
- McCune-Albright syndrom
- McKusick syndrom
- Melkersson-Rosenthal syndrom
- Menke’s syndrom
- Muckle-Wells syndrom
- Muir torre syndrom
- Nail-Patella syndrom
- Naxos sykdom
- Netherton syndrom
- Olmsted’s syndrom
- Pachonychia congenita
- PAPA syndrom
- Papillon-Lefevre syndrom
- Parington kutan amyloidose
- Parry-Romberg syndrom
- Peutz-Jeghers syndrom
- POEMS syndrom
- Progeria
- Proteus syndrom
- Pseudoxantoma elastikum
- Punktat palmoplantar keratodermi
- Reed syndrom
- Reticulate acropigmentation of Kitamura
- Richner-Hanhart syndrom
- Rothmund Thomson syndrom
- SAPHO syndrom
- Schnitzler syndrom
- Sjögren-Larsson syndrom
- Trigeminal trofisk syndrom
- Trousseau syndrom
- Turner syndrom
- Vohlwinkel’s syndrom
- Witkop syndrom
- X-Linked Dominant Chondrodysplasia Punctata
- Xeroderma pigmentosus
- Yellow nail syndrom
- Zinsser-Engman-Cole syndrom
Time til hudlege
Bestill time til hudlege enkelt online eller på telefon 22 03 21 00. Kort ventetid, erfarne spesialister og ingen henvisning.
Trousseau syndrom
Trousseau syndrom er en blodsykdom som gir overfladiske åreknutebetennelser, og øker risikoen for Trombose i blodkar. Syndromet kjennetegnes av gjentatte åreknutebetennelser.
Hva er årsaken til Trosseau syndrom?
Rundt halvparten av de med dette syndromet har en assosiert underliggende kreft som utløsende årsak. Kreft i bukspyttkjertelen og tarmen er vanligst. Ofte finner man ikke noen underliggende kreft eller annen årsak. En tror at det er en ubalanse i koagulasjonssystemet i blodet som gir symptomene.
Hvordan behandles tilstanden?
Om man klarer å identifisere en underliggende kreft, blir fokuset å behandle denne. Når kreften er fjernet vil også ofte symptomene ved Trousseau syndrom forsvinne. Blodfortynnende behandling med Heparin kan være til nytte i visse tilfeller.
Referanser
- Dermatology: 3rd edition. Bologna JL, Jorizzo JL (Eds.). Pub: Mosby.
- Rook’s Textbook of Dermatology. Burns DA, Breathnach SM (Eds.). Pub: Wiley-Blackwell.
- Andrew’s Diseases of the skin: Clinical Dermatology. James WD, Berger TG (Eds). Pub: Saunders
- Surgery of the Skin: Procedural Dermatology. Robinson JK, Hake CW (Eds).