Abstract:
:The authors present a case of a Sertoli-cell type androblastoma of the ovary. The tumor is mainly seen in young women and is mostly discovered through hormonal dysfunctions linked to it. Histopathological evaluation is indispensable for an exact diagnosis. Because of its rarity, there is little experience with the tumor and the histological identification is also sometimes very challenging. The tumor is occasionally associated with Peutz-Jeghers syndrome, tumor of the thyroid, or goiter. Biologically it follows a low-malignant course with a fair prognosis, long-term complex patient follow up is necessary after unilateral oophorectomy of the diseased organ.
journal_name
Orv Hetiljournal_title
Orvosi hetilapauthors
Istók R,Langmár Z,Szabó I,Glasz T,Székely E,Bánhidy F,Acs N,Paulin F,Magyar E,Schaff Zsubject
Has Abstractpub_date
2004-03-28 00:00:00pages
693-6issue
13eissn
0030-6002issn
1788-6120journal_volume
145pub_type
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