Multiple Endocrine Neoplasia Type 1

Multiple endocrine neoplasia type I (MEN I) is an inherited disorder in which tumors develop in several glands that produce hormones, mainly the parathyroids, the pituitary, and the pancreas.

Common causes: It originates from a genetic alteration that is passed down in families, so family history is a relevant piece of information.

Frequent symptoms: They may present variably depending on the glands affected, such as changes resulting from an excess of certain hormones or digestive discomfort.

Which specialist treats it? Its follow-up involves the endocrinologist, the general surgeon, and the oncologist, depending on the organ involved. If there is a family history of hormonal tumors, it is worth discussing it with a professional to guide timely monitoring.