Carcinoid Tumors and Medical Advancements

Carcinoid tumors, a subset of appendicular tumors, originate from neuroendocrine cells and can develop in various organs, including the lungs, intestines, and stomach. These tumors secrete hormones like serotonin, leading to carcinoid syndrome.

At A Glance

Treatment Options

Surgical Removal: The primary and most effective treatment for localized tumors.
Embolization Therapy: Used for metastatic tumors in the liver, this method helps in blocking the tumor’s blood supply.
Targeted Medications: Somatostatin analogs and chemotherapy can aid in managing tumor progression.

Prognosis: Patients diagnosed with early-stage carcinoid tumors often have a favorable outlook, with survival rates extending up to 10-15 years post-treatment.

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Therapeutic Areas of Focus

Neurology and Oncology

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