Steroid Cell Tumor of the Ovary in an Adolescent : A Rare Case Report

المؤلفون المشاركون

Selcuk, Ilker
Usubutun, Alp
Yusifli, Zarife
Gunalp, Serdar
Boyraz, Gokhan

المصدر

Case Reports in Medicine

العدد

المجلد 2013، العدد 2013 (31 ديسمبر/كانون الأول 2013)، ص ص. 1-3، 3ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2013-02-21

دولة النشر

مصر

عدد الصفحات

3

التخصصات الرئيسية

الطب البشري

الملخص EN

Steroid cell tumors (SCTs) of the ovary are a rare subgroup of sex cord tumors, account for less than 0.1% of all ovarian tumors, and also will present at any age.

These tumors can produce steroids, especially testosterone, and may give symptoms like hirsutism, hair loss, amenorrhea, or oligomenorrhea.

For the evaluation of androgen excess, testosterone and dehydroepiandrosterone sulfate (DHEA-S) are the first laboratory tests to be measured.

A pelvic ultrasound and a magnetic resonance imaging are useful radiologic imaging techniques.

Although steroid cell tumors are generally benign, there is a risk of malignant transformation and clinical malignant formation.

Surgery is the most important and hallmark treatment.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Boyraz, Gokhan& Selcuk, Ilker& Yusifli, Zarife& Usubutun, Alp& Gunalp, Serdar. 2013. Steroid Cell Tumor of the Ovary in an Adolescent : A Rare Case Report. Case Reports in Medicine،Vol. 2013, no. 2013, pp.1-3.
https://search.emarefa.net/detail/BIM-478829

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Boyraz, Gokhan…[et al.]. Steroid Cell Tumor of the Ovary in an Adolescent : A Rare Case Report. Case Reports in Medicine No. 2013 (2013), pp.1-3.
https://search.emarefa.net/detail/BIM-478829

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Boyraz, Gokhan& Selcuk, Ilker& Yusifli, Zarife& Usubutun, Alp& Gunalp, Serdar. Steroid Cell Tumor of the Ovary in an Adolescent : A Rare Case Report. Case Reports in Medicine. 2013. Vol. 2013, no. 2013, pp.1-3.
https://search.emarefa.net/detail/BIM-478829

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-478829