Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature

المؤلفون المشاركون

Wormald, B.
Elorbany, S.
Hanson, H.
Williams, J. W.
Heenan, S.
Barton, D. P. J.

المصدر

Case Reports in Obstetrics and Gynecology

العدد

المجلد 2018، العدد 2018 (31 ديسمبر/كانون الأول 2018)، ص ص. 1-4، 4ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2018-09-25

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الأمراض

الملخص EN

Sertoli-Leydig cell tumours of the ovary (SLCT) are rare tumours predominantly caused by mutations in the DICER1 gene.

We present a patient with a unilateral SLCT who had an underlying germline DICER1 gene mutation.

We discuss the underlying pathology, risks, and screening opportunities available to those with a mutation in this gene as SLCT is only one of a multitude of other tumours encompassing DICER1 syndrome.

The condition is inherited in an autosomal dominant fashion.

As such, genetic counselling is a key component of the management of women with SLCT.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Wormald, B.& Elorbany, S.& Hanson, H.& Williams, J. W.& Heenan, S.& Barton, D. P. J.. 2018. Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature. Case Reports in Obstetrics and Gynecology،Vol. 2018, no. 2018, pp.1-4.
https://search.emarefa.net/detail/BIM-1145933

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Wormald, B.…[et al.]. Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature. Case Reports in Obstetrics and Gynecology No. 2018 (2018), pp.1-4.
https://search.emarefa.net/detail/BIM-1145933

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Wormald, B.& Elorbany, S.& Hanson, H.& Williams, J. W.& Heenan, S.& Barton, D. P. J.. Sertoli-Leydig Cell Tumour and DICER1 Mutation: A Case Report and Review of the Literature. Case Reports in Obstetrics and Gynecology. 2018. Vol. 2018, no. 2018, pp.1-4.
https://search.emarefa.net/detail/BIM-1145933

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1145933