Every health problem has its own context. If you are hesitant about what is best for you, arrange a consultation. Our doctors will walk you through the situation and recommend a course of action that makes sense — professionally, sensitively, without unnecessary stress.
Adrenal tumors are often detected by chance — but sometimes the body sends signals that are worth paying attention to. If you experience these symptoms and manifestations for a long time, it is advisable to seek a specialist examination:
Adrenal tumor diseases encompass a wide range of conditions -- from frequent non-functional adenomas to rare hormone-active or malignant tumors. This section provides practical information to help quickly understand their diagnosis, clinical manifestations and treatment options. The texts are based on the latest recommendations and clinical experience of the team of Prof. Karel Pacák.
Accidentally found adrenal locus (>1 cm), requiring assessment of function, risk of malignancy and need for surgical solution.
Tumors producing catecholamines, often genetically determined. They can cause hypertension, palpitations and sweating.
A rare, aggressive tumor of the adrenal cortex. It can produce hormones and metastasize quickly. Requires rapid diagnosis and specialized treatment.
Adrenal tumors are rare, often hormonally active and genetically determined. They require specialized care and interdisciplinary cooperation.
Rare, often hormone-active tumors requiring interdisciplinary collaboration, genetic testing and specialized treatment in an experienced center.
A common finding in oncological patients, often asymptomatic. With bilateral involvement, there is a risk of severe adrenal insufficiency.
Metastatic involvement of the adrenal glands in oncological patients, often bilateral.
Do you want to know what is the most suitable solution for you? Are you a doctor or a patient and are you interested in Professor Pacák's expert opinion? Feel free to contact us.
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