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Fifth stage 

Gynecology 

Lec-7

 

د. احمد جاسم

 

6/4/2016

 

 

Sex cord-stromal tumour 

 

•  Sex cord-stromal tumour is a group of tumours of sex cord-derived tissues of the 

ovary and testis .It accounts for 8% of ovarian cancers and a minority of testicular 
cancers.
 

 

•  This group consists of: 

•  Granulosa cell tumour  

•  Thecoma  

•  Sertoli-Leydig cell tumour  

•  Fibroma  

•  These tumours tend to be functional ,producing estrogens or androgens .They may 

have dramatic clinical presentations. Almost all are unilateral. 

 

Granulosa cell tumour 

•  Granulosa cell tumo(u)rs  

( or granulosa-theca cell tumo(u)rs )are tumors of the 

granulosa cell .They are part of the sex cord-stromal tumour group of ovarian 
neoplasms.
 

•  The peak age at which they occur is 50-55 years, but they may occur at any age. 

 

Clinical presentation 

•  Estrogens are produced by functioning tumours, and the clinical presentation 

depends on the patient's age. 

•  If the patient is postmenopausal ,she usually presents with abnormal uterine 

bleeding . 

•  If the patient is of reproductive age ,she would present with menometrorrhagia .

However, in some cases she may stop ovulating altogether . 

•  If the patient has not undergone puberty ,isosexual-pseudo-precocity may be seen . 

 


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Histology 

•  The most characteristic gross appearance is a smooth surfaced solid and cystic lesion 

with the cysts filled with blood .Hemoperitoneum is an infrequent but classical 
presentation. A large variety of histological presentations exists, but they have two 
key features: 

•  Call-Exner bodies  

granulosa cells arranged haphazardly around a space containing 

eosinophilic fluid ;)and  

•  Pale uniform nuclei, often with grooves  

•  There have been cases where the tumor presented as a single, cyst-like, space, with 

no internal bleeding. 

 

Sertoli-Leydig cell tumour 

•  Sertoli-Leydig cell tumour ,also known as arrhenoblastoma or androblastoma ,is a 

member of the sex cord-stromal tumour group of ovarian and testicular cancers .
The tumour is rare, comprising less than 1% of ovarian tumours. While the tumour 
can occur at any age, it occurs most often in young adults. 

 

Classification 

•  The tumour is subdivided into many different subtypes. The most typical is composed 

of tubules lined by Sertoli cells and interstitial clusters of Leydig cells. 

 

Presentation 

•  Due to excess testosterone secreted by the tumour, one-third of female patients 

present with a recent history of progressive masculinization .Masculinization is 
preceded by anovulation ,oligomenorrhea ,amenorrhea and defeminization .
Additional signs include acne and hirsutism ,voice deepening ,clitoromegaly ,
temporal hair recession, and an increase in musculature. Serum testosterone level is 
high. 

 

Diagnosis 

•  A recent study has shown that CD56 can be a marker for tumors of this class. 

 

Treatment 

•  Treatment consists of surgical resection alone with a unilateral salpingo-

oophorectomy. The prognosis is generally good as the tumour tends to grow slowly 
and usually is benign

 :

25

%

 

are malignant. 




رفعت المحاضرة من قبل: Abdalmalik Abdullateef
المشاهدات: لقد قام 7 أعضاء و 99 زائراً بقراءة هذه المحاضرة








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