A rare case of aggressive, hereditary paraganglioma associated with a pathogenic variant in SDHD
Endokrynol Pol
.
2021;72(4):403.
doi: 10.5603/EP.a2021.0050.
Epub 2021 May 19.
Authors
Anna Kurzyńska
1
,
Elwira Przybylik-Mazurek
2
,
Anna Skalniak
1
,
Monika Buziak-Bereza
1
,
Agata Brzozowska-Czarnek
3
,
Romana Tomaszewska
4
,
Alicja Hubalewska-Dydejczyk
1
Affiliations
1
Clinical Department of Endocrinology, Jagiellonian University Medical College, Krakow, Poland.
2
Clinical Department of Endocrinology, Jagiellonian University Medical College, Krakow, Poland. elwira.przybylik-mazurek@uj.edu.pl.
3
Department of Radiology, Jagiellonian University Medical College, Krakow, Poland.
4
Department of Clinical and Experimental Pathology, Jagiellonian University Medical College, Krakow, Poland.
PMID:
34010450
DOI:
10.5603/EP.a2021.0050
Abstract
Not required for Clinical Vignette.
Keywords:
SDHD; alleles; paraganglioma; variants.
Publication types
Case Reports
MeSH terms
Germ-Line Mutation
Humans
Paraganglioma* / genetics
Succinate Dehydrogenase* / genetics
Substances
SDHD protein, human
Succinate Dehydrogenase