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Copyright 2001 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.2001
Figure 1. The lips are thick with nodules on the buccal mucosa at the angles of the mouth.
Figure 2. Nodules are noted lateral to an indented scar at the tip of the tongue from previous surgery.
Figure 3. DNA sequencing analysis of exon 16 of the RET proto-oncogene of the patient, her mother, sister, and control. A T→C transition in codon 918 is present in the patient; findings for the mother and sister were normal. This single point mutation results in the substitution of threonine for methionine (M918T) in the tyrosine kinase domain of the RET protein.
Multiple endocrine neoplasia 2B syndrome (MEN 2B) is a rare disorder inherited as an autosomal dominant trait. It is characterized by multiple mucosal neuromas, MTC, and pheochromocytoma.1
Characteristic findings on physical examination include elongated facies; mucosal neuromas on the lips, eyelids, buccal mucosa, tongue, palate, and intestinal mucous membranes; thickened medullated corneal nerves on slitlamp examination; marfanoid habitus; kyphoscoliosis; joint laxity; and pes cavus.2,3 Gastrointestinal manifestations, such as abdominal distension, feeding problems, dysphagia, vomiting, chronic constipation, intermittent abdominal pain, megacolon, and ganglioneuromatosis, may be seen in infancy.3 Constipation may suggest Hirschsprung disease.
Mucosal neuromas and MTC occur in all affected patients. A marfanoid habitus is present in 75% of patients, while enteric ganglioneuromatosis is found in more than 40% and pheochromocytoma in 50% of those affected.1 A main criterion for differentiation of MEN 2B from MEN 2A is the absence of mucosal neuromas in the latter.
Although full-blown manifestations of this disorder should facilitate recognition, in infancy or early childhood, when only gastrointestinal signs and symptoms are present, the diagnosis may be difficult. MEN 2B should be included in the differential diagnosis of chronic constipation in young children, and careful evaluation for clinical findings should be performed and genetic testing considered.3
Genetic alterations of the RET proto-oncogene have been identified in 95% to 98% of patients with MEN 2B, with a germline mutation most frequently at codon 9184,5 and, rarely, at codon 883.6 Screening is hampered because at least 50% of the cases are caused by de novo mutations.5
Total thyroidectomy is the primary treatment of MTC,7 which is almost universally bilateral and multifocal in MEN 2B cases and is associated with a high incidence of metastasis at the time of diagnosis.8 Extensive lymphadenectomy should be performed at the time of initial thyroidectomy, and reoperative lymphadenectomy must be considered in patients with persistently elevated calcitonin levels after thyroidectomy.7 Monitoring serum calcitonin levels is useful in identifying the occurrence of metastatic disease.
Early detection of individuals at risk for MEN 2B by genetic screening allows prophylactic thyroidectomy to be carried out before metastasis occurs. Because MTC has been diagnosed in a 6-month-old infant with MEN 2B,8 and metastatic MTC has been found in children younger than 5 years,9 prophylactic total thyroidectomy before age one2 or five10 years has been proposed.
The 5-year survival rate for MTC is 70% to 80%. Good prognostic factors are young age at diagnosis, female sex, occurrence in families, and tumor confinement to the thyroid gland.11 Periodic evaluation for pheochromocytoma should continue indefinitely after MEN 2B is identified.
Accepted for publication May 3, 2000.
This research was supported by NSC grant 88-2314-B-195-012 from the National Science Council, Executive Yuan, Taiwan.
Reprints: Tsen-Long Yang, MD, Department of Surgery, Mackay Memorial Hospital, 92 Chung-San N Rd, Section 2, Taipei 10449, Taiwan.
Picture of the Month. Arch Pediatr Adolesc Med. 2001;155(7):846. doi:10.1001/archpedi.155.7.845