SDHB-Associated Paraganglioma in a Pediatric Patient and Literature Review on Hereditary Pheochromocytoma-Paraganglioma Syndromes
Pheochromocytoma and paraganglioma are rare in the pediatric population occurring in approximately 1 in 50,000 children. While some cases are sporadic, they have commonly been associated with syndromes such as von Hippel-Lindau, multiple endocrine neoplasia types IIa and IIb, neurofibromatosis type...
Saved in:
Main Authors: | Heather Choat, Kerri Derrevere, Lisa Knight, Whitney Brown, Elizabeth H. Mack |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2014-01-01
|
Series: | Case Reports in Endocrinology |
Online Access: | http://dx.doi.org/10.1155/2014/502734 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Sex differences in presentation of pheochromocytoma and paraganglioma
by: Nora Azin Ali, et al.
Published: (2025-01-01) -
Simultaneous Pheochromocytoma, Paraganglioma, and Papillary Thyroid Carcinoma without Known Mutation
by: Lorena Rasquin, et al.
Published: (2018-01-01) -
Giant presacral paraganglioma
by: Chunhua Ma, et al.
Published: (2025-02-01) -
A 15-year pheochromocytoma and paraganglioma experience in a single centre: a Singapore perspective
by: Yingshan Lee, et al.
Published: (2022-11-01) -
Management of Hypertension in Intrapericardial Paraganglioma
by: Nicola Rotolo, et al.
Published: (2014-01-01)