Unilateralis Sertoli-sejtes androblastoma fiatal no petefé szkében

Roland Istók, Zoltán Langmár, István Szabó, Tibor Glasz, Eszter Székely, Ferenc Bánhidy, Nándor Ács, Ferenc Paulin, Éva Magyar, Zsuzsa Schaff

Research output: Review article


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.

Translated title of the contributionUnilateral Sertoli-cell type androblastoma in the ovary of a young woman
Original languageHungarian
Pages (from-to)693-696
Number of pages4
JournalOrvosi hetilap
Issue number13
Publication statusPublished - márc. 1 2004


  • Clinicopathology
  • Histopathology
  • Prognosis
  • Sertoli-cell androblastoma

ASJC Scopus subject areas

  • Medicine(all)

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  • Cite this

    Istók, R., Langmár, Z., Szabó, I., Glasz, T., Székely, E., Bánhidy, F., Ács, N., Paulin, F., Magyar, É., & Schaff, Z. (2004). Unilateralis Sertoli-sejtes androblastoma fiatal no petefé szkében. Orvosi hetilap, 145(13), 693-696.