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Hereditary paraganglioma-pheochromocytoma syndromes associated with SDHD and RET mutations

Choi, Do Woong Joseph; Tucker, Katherine M; Lee, Tack-Tsiew; Chong, Guan

Description

Background. Hereditary paraganglioma-pheochromocytoma syndromes (PGL/PCC) are rare tumors arising from neuroendocrine cells. Methods and Results. The proband, a 59-year-old white man and his 42-year-old elder son had a medical history of bilateral carotid body PGL and both presented for treatment of abdominal PGLs. His 36-year-old daughter had excision of recurrent malignant carotid body PGL and vertebral metastasis. His 33-year-old youngest son presented for excision of a unilateral carotid...[Show more]

CollectionsANU Research Publications
Date published: 2014
Type: Journal article
URI: http://hdl.handle.net/1885/53545
Source: Head and Neck
DOI: 10.1002/hed.23598

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