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Mycoplasma pneumoniae-associeret mukositis hos en 17-årig pige

Forfatter(e)
Mascha Eva Hildebrandt1, Anne Birgitte Alexius Agersted2, Tobias Steen Sejersen3 & Preben Homøe1
1) Øre-, Næse-, Hals- og Kæbekirurgisk Afdeling, Sjællands Universitetshospital, Køge 2) Pædiatrisk Afdeling, Sjællands Universitetshospital, Roskilde 3) Dermatologisk Afdeling, Sjællands Universitetshospital, Roskilde

Ugeskr Læger 2019;181:V07190377
Reference: 
Ugeskr Læger 2019;181:V07190377

Mascha Eva Hildebrandt, Anne Birgitte Alexius Agersted,
Tobias Steen Sejersen & Preben Homøe:

Mycoplasma pneumoniae-associated mucositis in a 17-year-old girl

Ugeskr Læger 2019;181:V07190377

Stevens-Johnson syndrome is an autoimmune condition characterised by erythematous target lesions on the skin with involvement of the oral and genital mucosa and conjunctivae. Recent case reports describe incomplete presentations with absence of the characteristic skin changes. This is caused by extrapulmonary manifestations of Mycoplasma pneumoniae lung infection and is now recognised as M. pneumoniae-associated mucositis (MPAM). This case report describes the clinical presentation of MPAM in a 17-year-old girl and highlights the importance of the recognition and the appropriate clinical management.

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