The clinical conundrum of a catecholamine secreting giant adrenal myelolipoma
Autor: | Satyadip Mukherjee, Tarun Jindal, Sandip Giri, Rajan Koju |
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Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: |
Myelolipoma
medicine.medical_specialty Pathology Myeloid Adrenal myelolipoma RD1-811 business.industry Adrenal cortex myelolipoma RC799-869 Diseases of the digestive system. Gastroenterology medicine.disease Surgery medicine.anatomical_structure adrenal Electrolyte imbalance catecholamine Urinary catecholamine Female patient medicine Catecholamine business medicine.drug |
Zdroj: | Journal of Minimal Access Surgery, Vol 18, Iss 1, Pp 139-141 (2022) |
ISSN: | 1998-3921 0972-9941 |
Popis: | Adrenal myelolipomas are uncommon tumours of unknown aetiology. They arise from the adrenal cortex and comprise lipomatous and myeloid elements. They are considered to be functionally inert, and metabolic evaluation is not mandatory for them. Adrenal myelolipomas can rarely be functionally active, and patients may present with hypertension, electrolyte imbalance or features of Cushing's syndrome. The association of these tumours with catecholamine secretion is exceptionally rare. We describe a case of a functional adrenal myelolipoma associated with catecholamine secretion in a 55-year-old female patient with a history of hypertension. The surgical excision of the mass resulted in normalisation of the urinary catecholamine levels and resolution of the hypertension. |
Databáze: | OpenAIRE |
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