Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Chapter 1: Histopathology of gynaecological cancers
Tubo-ovarian tumours – SCSTs

SCSTs are typically unilateral tumours and often hormonally active; the most common type is fibroma, which is benign.

A minority of tumours, granulosa cell tumours and Sertoli–Leydig cell tumours, may be malignant, and may recur many years after oophorectomy (Figure 1.4).

Gynaecological-Essentials-Fig1.4

Figure 1.4: Metastasis from adult granulosa cell tumour
Credit: Courtesy of the authors

Tumours are often hormonally active, causing endometrial neoplasia when oestrogens predominate and masculinisation when androgens predominate.

Granulosa cell tumours are classified as adult (more common, present in peri/postmenopausal women) or juvenile (rare, present in first 4 decades); they have different hormonal manifestations.

Tumours stain for inhibin, steroidogenic factor-1 (SF1), FOXL2 and calretinin, and are negative for epithelial membrane antigen (Figure 1.5).

Gynaecological-Essentials-Fig1.5

Figure 1.5: Immunostaining of granulosa cell tumour, adult type. 
Abbreviations: EMA, epithelial membrane antigen; SF1, steroidogenic factor-1
Credit: Courtesy of the authors

Point mutation in FOXL2 is characteristic of tumours of the adult type, and can aid diagnosis in challenging cases.

Sertoli–Leydig cell tumours have a wide age range at presentation. They can occur as either a combined tumour or be composed solely of Sertoli or Leydig cells (Figure 1.6)

Gynaecological-Essentials-Fig1.6

Figure 1.6: Sertoli–Leydig cell tumours
Credit: Courtesy of the authors

Sertoli tumours are morphologically heterogeneous, may contain heterologous elements, and are graded well, moderate or poorly differentiated, indicating increasing aggressiveness.

Tumours express sex cord-stromal immunomarkers and may carry mutations in DICER1 or FOXL2 genes.

Revision Questions

  1. Are the majority of SCSTs benign or malignant?
  2. What are the useful diagnostic stains for SCSTs?
  3. Are there any genetic tests used to classify these tumours?
Tubo-ovarian tumours – Classification and germ cell tumours (GCTs) Tubo-ovarian tumours – Epithelial tumours

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.