ArticleCentral European journal of urology2014
A spontaneous paraganglioma-pheochromocytoma syndrome.
Article in Central European journal of urology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Adrenergic crisis due to pheochromocytoma - practical aspects. A short review.Central European journal of urology · 2014Review
- Management and follow up of extra-adrenal phaeochromocytoma.Central European journal of urology · 2014Review
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8 authors.
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Abstract
We present a case of a 40-year old woman diagnosed with a four-place spontaneous paraganglioma-pheochromocytoma syndrome, which was treated surgically. The presence of the succinate dehydrogenase complex subunit D (SDHD) mutation that causes the pheochromocytoma was confirmed but no mutations in the family members were found. After the excision of the paragangliomas located in the areas of the division of carotid arteries, and mediastinum, as well as a tumor on the left site of the celiac trunk, the patient remains asymptomatic and is regularly followed-up.
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