Pediatric Malignant Pelvic Paraganglioma - A Diagnostic and Surgical Challenge

Tariq Rashid Salim Al-Shafei*, Farman Ali, Bashar Dawood, Zainab Al-Balushi, Jawaher Al Sulaimi, Alok Mittal, Dhruva N. Ghosh

*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلةArticleمراجعة النظراء

ملخص

Pheochromocytoma are chromaffin cell-derived tumors that have an exceptionally high genetic predisposition. The presentation of extra-adrenal and pelvic paraganglioma (PGL) in children is uncommon. Due to the relative rarity, PGL tumors' presentation and disease behavior may vary. Genetic testing, imaging, and biochemical investigation are employed to diagnose PGL. Surgical resection with preoperative angioembolization has been practiced in alleviating the burden of torrential intraoperative bleeding.

اللغة الأصليةEnglish
الصفحات (من إلى)E833-E836
دوريةJournal of Pediatric Hematology/Oncology
مستوى الصوت45
رقم الإصدار7
المعرِّفات الرقمية للأشياء
حالة النشرPublished - أغسطس 17 2023

ASJC Scopus subject areas

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