TY - JOUR
T1 - Paragangliomes malins héréditaires
T2 - problèmes liés à la prise en charge des formes non sécrétantes
AU - Bonnet, S.
AU - Durand, X.
AU - Baton, O.
AU - Gimenez-Roqueplo, A. P.
AU - Baudin, E.
AU - Visset, J.
AU - Algayres, J. P.
AU - Baranger, B.
PY - 2006/12/1
Y1 - 2006/12/1
N2 - Non-functional paraganglioma have not clinical or biological characteristics, so that the diagnostic is most of the time delayed and made on the occasion of advanced abdominal tumor or symptomatic metastasis management. Hereditary forms, notably those with SDHB mutation, seem to have a poor prognosis. On the other hand, and on the oposite to sporadic forms, they are the only ones to benefit from genetic testing which make possible, if positive, an earlier diagnostic, before apparition of symptoms, recurrence or metastasis. We report a case of non-functional malignant hereditary paraganglioma diagnosed belatedly and we will consider management problems raised by non-functional forms.
AB - Non-functional paraganglioma have not clinical or biological characteristics, so that the diagnostic is most of the time delayed and made on the occasion of advanced abdominal tumor or symptomatic metastasis management. Hereditary forms, notably those with SDHB mutation, seem to have a poor prognosis. On the other hand, and on the oposite to sporadic forms, they are the only ones to benefit from genetic testing which make possible, if positive, an earlier diagnostic, before apparition of symptoms, recurrence or metastasis. We report a case of non-functional malignant hereditary paraganglioma diagnosed belatedly and we will consider management problems raised by non-functional forms.
KW - Genetic testing
KW - Malignant hereditary paraganglioma
KW - Metastasis
KW - Non-functional paraganglioma
KW - SDHB mutation
UR - http://www.scopus.com/inward/record.url?scp=33947510107&partnerID=8YFLogxK
U2 - 10.1016/j.anchir.2006.05.004
DO - 10.1016/j.anchir.2006.05.004
M3 - Article
C2 - 16815237
AN - SCOPUS:33947510107
SN - 0003-3944
VL - 131
SP - 626
EP - 630
JO - Annales de Chirurgie
JF - Annales de Chirurgie
IS - 10
ER -