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Type of manuscrit : Original articles Titre: Clinical and Therapeutic Profile of Pheochromocytomas and Paragangliomas: A 20- Year Cohort from Algeria

2026-06-09

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<title>Abstract</title> <p>Introduction : Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors arising from chromaffin cells of the adrenal medulla or from sympathetic and parasympathetic ganglia. Their heterogeneous clinical presentation often leads to diagnostic delay and exposes patients to significant cardiovascular morbidity. <h4>Methods:</h4> We conducted a retrospective, descriptive...

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Literature Corpus work: 776d31b5-cade-5bf2-b5e6-1fd9254e5ac7
DOI: 10.21203/rs.3.rs-9607931/v1

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