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Malignt pleuralt mesoteliom

Forfatter(e)

Sajitha Sophia Sritharan1, 2, Jens Lundby Frandsen2, Øyvind Omland3 & Jens Meldgaard Bruun2

1) Lungemedicinsk Afdeling, Aarhus Universitetshospital 2) Medicinsk Afdeling, Regionshospitalet Randers 3) Det Sundhedsvidenskabelige Fakultet, Klinisk Institut, Arbejdsmedicin, Aalborg Universitetshospital Ugeskr Læger 2018;180:V06170439

Reference: 
Ugeskr Læger 2018;180:V06170439
Blad nummer: 
Sidetal: 
2-6
Malignant pleural mesothelioma

Malignant pleural mesothelioma (MPM) is a rare cancer with a poor prognosis. The disease is of importance, since the incidence in Denmark is increasing despite cessation of the use of asbestos in the 1980s. MPM has a long latency period, and the first symptom is often dyspnoea, typically caused by pleural effusion. The diagnosis is a challenge, because cytology often is non-conclusive, and thoracoscopy is needed to obtain biopsies for immunohistochemistry. The occupational history is important, since the patients are entitled to compensation. The treatment is often limited to palliation.

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