Literature DB >> 16815237

[Malignant hereditary paraganglioma: problems raised by non-functional forms management].

S Bonnet1, X Durand, O Baton, A-P Gimenez-Roqueplo, E Baudin, J Visset, J-P Algayres, B Baranger.   

Abstract

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.

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Year:  2006        PMID: 16815237     DOI: 10.1016/j.anchir.2006.05.004

Source DB:  PubMed          Journal:  Ann Chir        ISSN: 0003-3944


  3 in total

1.  Successful chemotherapy of hepatic metastases in a case of succinate dehydrogenase subunit B-related paraganglioma.

Authors:  J He; D Makey; T Fojo; K T Adams; B Havekes; G Eisenhofer; P Sullivan; E W Lai; K Pacak
Journal:  Endocrine       Date:  2009-07-18       Impact factor: 3.633

2.  Biochemically silent abdominal paragangliomas in patients with mutations in the succinate dehydrogenase subunit B gene.

Authors:  Henri J L M Timmers; Karel Pacak; Thanh T Huynh; Mones Abu-Asab; Maria Tsokos; Maria J Merino; Bora E Baysal; Karen T Adams; Graeme Eisenhofer
Journal:  J Clin Endocrinol Metab       Date:  2008-10-07       Impact factor: 5.958

Review 3.  Clinical aspects of SDHx-related pheochromocytoma and paraganglioma.

Authors:  Henri J L M Timmers; Anne-Paule Gimenez-Roqueplo; Massimo Mannelli; Karel Pacak
Journal:  Endocr Relat Cancer       Date:  2009-02-03       Impact factor: 5.678

  3 in total

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