
To Contact: +91-9810753843, +91-6388422267
By Appointment Only:
Medicos Surgical Clinic, #6, Sector 11 A, Chandigarh, Monday to Friday, 4-7pm
MEN SYNDROME
MEN (Multiple Endocrine Neoplasia) is a genetic disorder in which a person develops tumors in multiple hormone-producing glands of the body.
These tumors may be:
-
Benign (non-cancer)
-
Cancerous
-
Overproduce hormones → cause many symptoms

FAQS
Which glands are usually involved?
-
Parathyroid glands – control calcium
-
Pituitary gland – controls many hormones
-
Pancreas (endocrine part) – insulin, gastrin, etc.
-
Thyroid gland
-
Adrenal glands
Q3. Are there different types of MEN?
Yes. Mainly MEN 1 and MEN 2.
MEN TYPE 1 (MEN 1)
Q4. What is MEN 1 also called?
“3 P Syndrome” because it affects:
-
Parathyroid
-
Pancreatic endocrine tumors
-
Pituitary
Q5. What symptoms occur in MEN 1?
1. Parathyroid Tumors (Most Common)
-
High calcium
-
Kidney stones
-
Bone pain
-
Constipation
-
Weakness
-
Depression
2. Pancreatic Endocrine Tumors
Depends on hormone:
Tumor Symptoms
Insulinoma Low sugar, sweating, fainting
Gastrinoma Severe ulcers, acidity
Glucagonoma Weight loss, rash, diabetes
3. Pituitary Tumors
-
Headache
-
Vision problems
-
Irregular periods
-
Milk discharge
-
Infertility
Q6. What is the genetic cause of MEN 1?
-
MEN1 gene mutation
-
Autosomal Dominant → 50% chance to children
-
Family screening is very important
MEN TYPE 2 (MEN 2)
Q7. What glands are involved in MEN 2?
-
Thyroid (Medullary Thyroid Cancer)
-
Adrenal (Pheochromocytoma)
-
Parathyroid (sometimes)
Q8. Types of MEN 2?
-
MEN 2A
-
MEN 2B
-
Familial Medullary Thyroid Cancer (FMTC)
Q9. Symptoms of MEN 2
Medullary Thyroid Cancer
-
Neck swelling
-
Difficulty swallowing
-
Hoarseness
-
Lymph node enlargement
Pheochromocytoma
-
Headache
-
Sweating
-
Palpitations
-
High BP
MEN 2B Additional Features
-
Thick lips
-
Tongue nodules
-
Tall thin body
-
Intestinal problems
Q10. Genetic Cause of MEN 2
-
RET gene mutation
-
Autosomal Dominant inheritance
-
Genetic testing is crucial
DIAGNOSIS OF MEN SYNDROME
Q11. How is MEN diagnosed?
1. Blood Tests
-
Calcium
-
Hormone levels
-
Calcitonin
-
Insulin, Gastrin, Prolactin
2. Imaging
-
Ultrasound
-
CT / MRI
-
Nuclear scans
3. Genetic Testing
-
Very important
-
Tests family members
-
Detects disease early
ROLE OF SURGERY IN MEN
Surgery is often the main treatment.
MEN 1 – Surgery
Parathyroid
-
Subtotal or Total Parathyroidectomy
-
Most common surgery
Pancreatic Tumors
-
Tumor removal
-
Sometimes partial pancreas removal
Pituitary
-
Brain surgery through nose (Transsphenoidal)
MEN 2 – Surgery
Thyroid (Very Important)
-
Total Thyroidectomy
-
Often done preventively in children with RET mutation
Adrenal (Pheochromocytoma)
-
Adrenalectomy
-
Must control BP before surgery
FOLLOW-UP IN MEN SYNDROME
Q12. Why is follow-up important?
Because tumors can:
-
Recur
-
Appear in new glands
-
Become cancerous
Q13. What follow-up is needed?
Life-long monitoring:
-
Blood tests yearly
-
Hormone levels
-
Imaging scans
-
Genetic counseling
-
Family screening
Final Take-Home Message
-
MEN is genetic and lifelong.
-
Early diagnosis + genetic testing saves lives.
-
Surgery plays a major role, especially thyroid and parathyroid surgery.
-
Regular follow-up and family screening are essential.
CONSULT WITH EXPERTS
BY APPOINTMENT ONLY:
MEDICOS SURGICAL CLINIC, #6, SEC 11A, CHANDIGARH, MONDAY TO FRIDAY 5-7PM
CONTACT +91-9810753843