Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome

المؤلفون المشاركون

Pugh, Jessica
Huffaker, R. Keith

المصدر

Case Reports in Urology

العدد

المجلد 2017، العدد 2017 (31 ديسمبر/كانون الأول 2017)، ص ص. 1-3، 3ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2017-04-11

دولة النشر

مصر

عدد الصفحات

3

التخصصات الرئيسية

الطب البشري

الملخص EN

A 22-year-old nulligravid white female with Angelman syndrome was noted to have a 4-month history of premenstrual nausea, vomiting, and abdominal pain.

She had an echogenic focus in her bladder noted on ultrasound.

She was diagnosed with low grade urothelial carcinoma after cystoscopic evaluation with biopsy and was sent to urology for further treatment.

Urothelial carcinoma is rare in individuals younger than age 40.

Patients may present with gross hematuria.

There is often a delay in diagnosis in younger individuals with different genetic mutations noted upon diagnosis.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Pugh, Jessica& Huffaker, R. Keith. 2017. Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome. Case Reports in Urology،Vol. 2017, no. 2017, pp.1-3.
https://search.emarefa.net/detail/BIM-1150617

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Pugh, Jessica& Huffaker, R. Keith. Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome. Case Reports in Urology No. 2017 (2017), pp.1-3.
https://search.emarefa.net/detail/BIM-1150617

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Pugh, Jessica& Huffaker, R. Keith. Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome. Case Reports in Urology. 2017. Vol. 2017, no. 2017, pp.1-3.
https://search.emarefa.net/detail/BIM-1150617

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1150617