Multiple Endocrine Neoplasia Type 2

Multiple endocrine neoplasia type II (MEN II) is an inherited syndrome that predisposes to the development of tumors in endocrine glands, especially the thyroid, the adrenals, and the parathyroids.

Common causes: It stems from a genetic alteration passed down in families, so knowing the family history helps guide monitoring.

Frequent symptoms: The manifestations depend on the glands affected and include changes associated with excessive hormone production or alterations in blood pressure.

Which specialist treats it? The endocrinologist coordinates the hormonal study, while the general surgeon and the oncologist take part depending on the tumors present. When there is a family history of this type of condition, it is advisable to approach a professional who can define personalized follow-up.