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Multiple Endocrine Neoplasia (MEN) Syndromes PDQ®
Guideline · Mar 2020 · 1 min read
In brief
In brief
NCI's evidence-based clinical reference for healthcare professionals managing childhood Multiple Endocrine Neoplasia syndromes. Covers genetic basis, diagnostic criteria, surveillance protocols, and treatment approaches for MEN-related endocrine tumors in pediatric patients.
- MEN syndromes are hereditary conditions causing tumors in multiple endocrine glands, requiring lifelong surveillance.
- Early genetic testing in at-risk families enables proactive screening and timely intervention before malignancy develops.
- Multidisciplinary care coordination is essential given the multi-organ involvement across endocrinology, surgery, and oncology.
Written by the GCMD Library team from the guideline.
National Institute of Health and National Cancer Institute Childhood Multiple Endocrine Neoplasia (MEN) Syndromes Treatment (PDQ®)–Health Professional Version
This guideline lives on cancer.gov.
Open it on cancer.gov ↗Educational content from recorded physician discussions — not medical advice. Talk to your (or your child's) care team about your situation.
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