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Monitoring of kindreds with hereditary predisposition for cutaneous melanoma and dysplastic nevus syndrome: results of a Swedish preventive program

Hansson, J. (författare)
Karolinska Institutet
Bergenmar, M. (författare)
Karolinska Institutet
Hofer, P. A. (författare)
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Lundell, G. (författare)
Karolinska Institutet
Mansson-Brahme, E. (författare)
Karolinska Institutet
Ringborg, U. (författare)
Karolinska Institutet
Synnerstad, Ingrid (författare)
Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Dermatologi och venerologi,Hudkliniken i Östergötland
Bratel, A. T. (författare)
Wennberg, Ann-Marie, 1956 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Rosdahl, Inger (författare)
Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Dermatologi och venerologi,Hudkliniken i Östergötland
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 (creator_code:org_t)
2007
2007
Engelska.
Ingår i: J Clin Oncol. ; 25:19, s. 2819-2824
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • PURPOSE: To evaluate a program initiated in 1987 by the Swedish Melanoma Study Group aiming to provide preventive surveillance to kindreds with hereditary cutaneous melanoma and dysplastic nevus syndrome. PATIENTS AND METHODS: Overall, 2,080 individuals belonging to 280 melanoma families were followed for 14 years between 1987 and 2001 at 12 participating centers. Data were registered in a central database. RESULTS: Among 1,912 skin lesions excised during follow-up, 41 melanomas were removed in 32 individuals. Of these, 15 (37%) were in situ melanomas and 26 (63%) invasive melanomas. The median tumor thickness of invasive melanomas was 0.5 mm. Ulceration was absent in 24 of 26 invasive melanomas (92%) and 12 (46%) lacked vertical growth phase. Compared with melanomas in the general Swedish population, the melanomas identified in these kindreds during follow-up had better prognostic characteristics. All melanomas except one were diagnosed in families with two or more first-degree relatives with melanoma. Diagnosis of melanoma occurred in three of eight kindreds with germline CDKN2A mutations, supporting that families with such mutations are at increased risk for melanoma development. Of the 32 individuals who developed melanoma during follow-up, 21 (66%) had had at least one previously diagnosed melanoma. CONCLUSION: This study shows that a coordinated program aimed at detecting and offering skin surveillance in kindreds with hereditary cutaneous melanoma results in a low incidence of melanomas during the follow-up period and that the tumors that do arise have favorable prognostic characteristics.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Dermatologi och venereologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dermatology and Venereal Diseases (hsv//eng)

Nyckelord

Adolescent
Adult
Aged
Aged
80 and over
Child
Cyclin-Dependent Kinase Inhibitor p16/genetics
Dysplastic Nevus Syndrome/complications/*genetics/*prevention & control
Family Health
Female
*Genetic Predisposition to Disease
Humans
Male
Melanoma/complications/*genetics/*prevention & control
Middle Aged
Skin Neoplasms/complications/*genetics/*prevention & control
Sweden
MEDICINE

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