Diagnostic challenge of fetal ontogeny and its application on the ovarian teratomas

Nam Hoon Cho, Young Tae Kim, Ji Hwan Lee, Chanil Song, Sung Woo Cho, Sang Ho Cho, Je Geun Chi

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Although neuroepithelial tubules (NET) often are a component of immature teratoma (IT), they are not always required for diagnosis. Other somatic elements are sufficient and often verified with immunohistochemical stain. This study was designed to determine the definition of immaturity versus fetal ontogeny, using several molecular markers in IT. It is our contention that IT is equivalent to an embryonic stage less than a fertilization age (FA) of 8 weeks, and a mature teratoma (MT) to a fetal stage later than a FA of 8 weeks, whereas an embryonal carcinoma (Eca) matches a pre-embryonic stage earlier than a FA of 2 weeks. The teratomatous components used as a roadmap to evaluate maturity included: a lobular structure of primitive endodermal tubules (FA 4 +4 to 6 weeks), a ventricle-lined cortical plate (FA 9 weeks), a complex papillary choroid plexus (FA 10 weeks), melanin deposition in hair follicles (FA 15 weeks), and the bell stage of odontogenesis (FA 19 weeks). The teratomatous components of 25 resected ovarian solid teratoma samples were compared with fetal ontogeny. For an immunohistochemical analysis, the CD30, CD34, CD99, bcl-2, alpha-fetoprotein (AFP), and placenta-like alkaline phosphatase (FLAP) were assessed. The AFP and Ki-1 were positive in the embryoid body, which was identified at a FA less than 4 weeks in Eca. The AFP was positive in the primitive endodermal components and some of the squamous epithelium in IT. The CD99 and bcl-2 were selectively stained in the primitive NET, which was detected no later than a FA of 6 weeks. The CD34 and bcl-2 were positive in the immature-looking precartilage blastomatous components, which proved useful for detecting immature cartilage, corresponding to a FA of 5 to 6 weeks. The ontogeny of IT was found to correspond to the embryonic stage at a FA of 2 to 8 weeks, and CD99, CD34, bcl-2, AFP, CD30, and FLAP could be used as supportive tools to define IT. This new grading system could be more scientific and more reproducible in any spectra of teratoma.

Original languageEnglish
Pages (from-to)173-182
Number of pages10
JournalInternational Journal of Gynecological Pathology
Volume24
Issue number2
DOIs
Publication statusPublished - 2005 Apr 1

Fingerprint

Fertilization
Teratoma
alpha-Fetoproteins
Embryonal Carcinoma
Placenta
Alkaline Phosphatase
Ovarian Teratoma
Odontogenesis
Embryoid Bodies
Choroid Plexus
Hair Follicle
Melanins
Cerebral Cortex
Cartilage
Coloring Agents
Epithelium

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Obstetrics and Gynaecology

Cite this

Cho, Nam Hoon ; Kim, Young Tae ; Lee, Ji Hwan ; Song, Chanil ; Cho, Sung Woo ; Cho, Sang Ho ; Chi, Je Geun. / Diagnostic challenge of fetal ontogeny and its application on the ovarian teratomas. In: International Journal of Gynecological Pathology. 2005 ; Vol. 24, No. 2. pp. 173-182.
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Diagnostic challenge of fetal ontogeny and its application on the ovarian teratomas. / Cho, Nam Hoon; Kim, Young Tae; Lee, Ji Hwan; Song, Chanil; Cho, Sung Woo; Cho, Sang Ho; Chi, Je Geun.

In: International Journal of Gynecological Pathology, Vol. 24, No. 2, 01.04.2005, p. 173-182.

Research output: Contribution to journalArticle

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