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Sex cord–gonadal stromal tumour

Sex cord–gonadal stromal tumour is a biology topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Sex cord–gonadal stromal tumour rather than just read about it. In short: Sex cord–gonadal stromal tumour is a group of tumours derived from the stromal component of the ovary and testis, which comprises the granulosa, thecal cells and fibrocytes. In contrast, the epithelial cells originate from the outer epithelial lining surrounding the gonad while the germ cell tumors arise from the precursor cells of the gametes, hence the name germ cell.

Sex cord–gonadal stromal tumour — main illustration
Sex cord–gonadal stromal tumour — illustration

Key takeaways

  • Sex cord–gonadal stromal tumour belongs to biology; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Sex cord–gonadal stromal tumour to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Sex cord–gonadal stromal tumour from memory before moving on to harder problems.

Reference excerpt

Sex cord–gonadal stromal tumour is a group of tumours derived from the stromal component of the ovary and testis, which comprises the granulosa, thecal cells and fibrocytes. In contrast, the epithelial cells originate from the outer epithelial lining surrounding the gonad while the germ cell tumors arise from the precursor cells of the gametes, hence the name germ cell. In humans, this group accounts for 8% of ovarian cancers and under 5% of testicular cancers. Their diagnosis is histological: only a biopsy of the tumour can make an exact diagnosis. They are often suspected of being malignant prior to operation, being solid ovarian tumours that tend to occur most commonly in post menopausal women. This group of tumours is significantly less common than testicular germ cell tumours in men, and slightly less common than ovarian germ cell tumours in women (see Ovarian cancer).

Types

Tumour types in order of prevalence Granulosa cell tumour. This tumour produces granulosa cells, which normally are found in the ovary. It is malignant in 20% of women diagnosed with it. It tends to present in women in the 50-55yo age group with post menopausal vaginal bleeding. Uncommonly, a similar but possibly distinct tumour, juvenile granulosa cell tumour, presents in pre-pubertal girls with precocious puberty. In both groups, the vaginal bleeding is due to oestrogen secreted by the tumour. In older women, treatment is total abdominal hysterectomy and removal of both ovaries. In young girls, fertility sparing treatment is the mainstay for non-metastatic disease. Sertoli cell tumour. This tumour produces Sertoli cells, which normally are found in the testicle. This tumour occurs in both men and women. Thecoma. This tumour produces theca of follicle, a tissue normally found in the ovarian follicle. The tumour is almost exclusively benign and unilateral. It typically secretes estrogen, and as a result women with this tumour often present with postmenopausal bleeding. Leydig cell tumour. This tumour produces Leydig cells, which normally are found in the testicle and tend to secrete androgens. Sertoli–Leydig cell tumour. This tumour produces both Sertoli and Leydig cells. Although both cell types normally occur in the testicle, this tumour can occur in the ovary. Gynandroblastoma. A very rare tumour producing both ovarian (granulosa and/or theca) and testicular (Sertoli and/or Leydig) cells or tissues. Typically it consists of adult-type granulosa cells and Sertoli cells, but it has been reported with juvenile-type granulosa cells. It has been reported to occur in the ovary usually, rarely in the testis. Due to its rarity, the malignant potential of this tumour is unclear; there is one case report of late metastasis. Sex cord tumour with annular tubules, abbreviated SCTAT. These are rare tumours that may be sporadic or associated with Peutz–Jeghers syndrome.

Diagnosis Definitive diagnosis of these tumours is based on the histology of tissue obtained in a biopsy or surgical resection. In a retrospective study of 72 cases in children and adolescents, the histology was important to prognosis. A number of molecules have been proposed as markers for this group of tumours. CD56 may be useful for distinguishing sex cord–stromal tumours from some other types of tumours, although it does not distinguish them from neuroendocrine tumours. Calretinin has also been suggested as a marker. For diagnosis of granulosa cell tumour, inhibin is under investigation. Granulosa cell tumours and Sertoli-Leydig cell tumours have specific genetic mutations that are characteristic and can help support the diagnosis. On magnetic resonance imaging, a fibroma may produce one of several imaging features that might be used in the future to identify this rare tumour prior to surgery.

Prognosis A retrospective study of 83 women with sex cord–stromal tumours (73 with granulosa cell tumour and 10 with Sertoli-Leydig cell tumour), all diagnosed between 1975 and 2003, reported that survival was higher with age under 50, smaller tumour size, and absence of residual disease. The study found no effect of chemotherapy. A retrospective study of 67 children and adolescents reported some benefit of cisplatin-based chemotherapy.

Research A prospective study of ovarian sex cord–stromal tumours in children and adolescents began enrolling participants in 2005. The International Ovarian and Testicular Stromal Tumor Registry is studying these rare tumours and collecting data on them to further research. Targeted treatments are being evaluated for these tumours as well.

See also Sex cord Stroma of ovary

References

External links Media related to Sex cord–gonadal stromal tumors at Wikimedia Commons

Illustrations

Sex cord–gonadal stromal tumour illustration
Sex cord–gonadal stromal tumour: Ovarian tumours by incidence and risk of ovarian cancer, with sex cord-stromal tumours at right.[3]
Ovarian tumours by incidence and risk of ovarian cancer, with sex cord-stromal tumours at right.[3]
Sex cord–gonadal stromal tumour illustration
Sex cord–gonadal stromal tumour illustration
Sex cord–gonadal stromal tumour illustration

Worked examples

Example 1 — a first encounter with Sex cord–gonadal stromal tumour

Start with the simplest possible case. Write down what Sex cord–gonadal stromal tumour claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In biology, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Sex cord–gonadal stromal tumour before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Sex cord–gonadal stromal tumour ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Sex cord–gonadal stromal tumour

In research
Sex cord–gonadal stromal tumour appears in biology research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Sex cord–gonadal stromal tumour in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Sex cord–gonadal stromal tumour is common in secondary-school and first-year university syllabi. It links to neighbouring topics Gynaecological cancer, Male genital neoplasia, Ovarian cancer, so understanding it makes those chapters shorter.
In everyday life
Look for Sex cord–gonadal stromal tumour outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study Sex cord–gonadal stromal tumour in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Sex cord–gonadal stromal tumour means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Sex cord–gonadal stromal tumour out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Sex cord–gonadal stromal tumour in simple terms?

Sex cord–gonadal stromal tumour is a group of tumours derived from the stromal component of the ovary and testis, which comprises the granulosa, thecal cells and fibrocytes. In contrast, the epithelial cells originate from the outer epithelial lining surrounding the gonad while the germ cell tumors…

Why does Sex cord–gonadal stromal tumour matter?

Because it connects several biology ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Sex cord–gonadal stromal tumour?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Sex cord–gonadal stromal tumour.

Tags

  • Gynaecological cancer
  • Male genital neoplasia
  • Ovarian cancer

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