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Avoiding harmful procedures in patients with elevated α-fetoprotein concentrations: Hereditary persistence of α-fetoprotein is an important and benign differential diagnosis!

  • Walter Bonfig
  • , Maja Hempel
  • , Irene Teichert-Von Lüttichau
  • , Susanne Liptay
  • , Stefan Burdach
  • Technical University of Munich

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

BACKGROUND: Hereditary persistence of α-fetoprotein (AFP) is a rare but benign condition. OBSERVATION: A 13-year-old girl presented with dysmenorrhoic complaints and irregular cycles. Diagnostic workup revealed a cystic lesion of the ovary and elevated AFP; β-human chorionic gonadotrophin was negative. Right-sided ovarectomy was performed. Postsurgery AFP concentration did not decline. The patient underwent further diagnostic workup with negative results. Histology revealed follicular cysts but no tumor. Finally, hereditary persistence of AFP was suspected and AFP testing was performed in the family. CONCLUSIONS: It is important to include hereditary persistence of AFP in the differential diagnosis of elevated AFP concentrations to avoid harmful procedures.

Original languageEnglish
Pages (from-to)e301-e303
JournalJournal of Pediatric Hematology/Oncology
Volume34
Issue number7
DOIs
StatePublished - Oct 2012

Keywords

  • malignancy screening
  • tumor marker
  • α-fetoprotein

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