{"id":11610,"date":"2025-07-26T10:26:28","date_gmt":"2025-07-26T08:26:28","guid":{"rendered":"https:\/\/valintermed.com\/?p=11610"},"modified":"2025-07-26T10:26:28","modified_gmt":"2025-07-26T08:26:28","slug":"nasledstvennyy-sindrom-paragangliomy-feohromotsitomy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/hereditary-paragangliomatosis-syndrome\/","title":{"rendered":"Hereditary paraganglioma-pheochromocytoma syndrome"},"content":{"rendered":"
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Paragangliomas and pheochromocytomas are rare tumors that arise from chromaffin cells, which are responsible for the synthesis and release of catecholamines such as epinephrine and norepinephrine. These tumors can develop in a variety of locations, including the adrenal glands and in the paraganglia located along the sympathetic nervous system. Hereditary paraganglioma-pheochromocytoma syndrome is a genetic predisposition to develop these tumors and is associated with various genetic mutations that result in an increased risk of their occurrence. This syndrome can present as multiple tumors, which greatly complicates the clinical picture and requires careful monitoring and diagnosis.<\/p>\n

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