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Rozhl Chir ; 73(7): 339-41, 1994 Nov.
Artigo em Eslovaco | MEDLINE | ID: mdl-7817253

RESUMO

The authors present a report on a new clinical and pathological entity--aggressive angiomyxoma which was described in 1983. They draw attention to the genesis of this tumour and its macro- and microscopic picture. They emphasize that treatment of this tumour involves its complete surgical extirpation and frequent local relapses without secondaries. The authors describe in detail two of their observations of aggressive angiomyxoma in a 32- an 38-year-old woman where the tumour started in the lesser pelvis. In both instances, despite radical extirpation of the tumour, within a relatively short time a local relapse developed detected by USG and CT without clinical symptoms.


Assuntos
Mixoma , Neoplasias Pélvicas , Adulto , Feminino , Humanos , Mixoma/patologia , Neoplasias Pélvicas/patologia
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