- Open Access
Multiple endocrine neoplasias type 2B and RET proto-oncogene
© Martucciello et al; licensee BioMed Central Ltd. 2012
Received: 30 January 2012
Accepted: 19 March 2012
Published: 19 March 2012
Multiple Endocrine Neoplasia type 2B (MEN 2B) is an autosomal dominant complex oncologic neurocristopathy including medullary thyroid carcinoma, pheochromocytoma, gastrointestinal disorders, marphanoid face, and mucosal multiple ganglioneuromas. Medullary thyroid carcinoma is the major cause of mortality in MEN 2B syndrome, and it often appears during the first years of life. RET proto-oncogene germline activating mutations are causative for MEN 2B. The 95% of MEN 2B patients are associated with a point mutation in exon 16 (M918/T). A second point mutation at codon 883 has been found in 2%-3% of MEN 2B cases. RET proto-oncogene is also involved in different neoplastic and not neoplastic neurocristopathies. Other RET mutations cause MEN 2A syndrome, familial medullary thyroid carcinoma, or Hirschsprung's disease. RET gene expression is also involved in Neuroblastoma. The main diagnosis standards are the acetylcholinesterase study of rectal mucosa and the molecular analysis of RET. In our protocol the rectal biopsy is, therefore, the first approach. RET mutation detection offers the possibility to diagnose MEN 2B predisposition at a pre-clinical stage in familial cases, and to perform an early total prophylactic thyroidectomy. The surgical treatment of MEN 2B is total thyroidectomy with cervical limphadenectomy of the central compartment of the neck. When possible, this intervention should be performed with prophylactic aim before 1 year of age in patients with molecular genetic diagnosis. Recent advances into the mechanisms of RET proto-oncogene signaling and pathways of RET signal transduction in the development of MEN 2 and MTC will allow new treatment possibilities.
Multiple Endocrine Neoplasia Type 2 B (MEN 2B) is a rare autosomal dominant complex neoplastic neurocristopathy characterized by the development of a number of tumors including medullary thyroid carcinoma (MTC) and pheochromocytoma (Pheo) with gastrointestinal symptoms, marphanoid facies and multiple ganglioneuromas (GN)/ganglioneurofibromas(GNf) . MTC is present in 100% of MEN 2B cases, and it often already appears in the 1st decade of life . MTC is the main cause of death in MEN 2B patients who don't receive early or prophylactic treatment. Surgical treatment of MTC is the only effective therapy in cases with localized tumor.
Molecular analysis of the RET gene (RE arranged during T ransfection) has changed the history of this syndrome, as it allows the identification of MEN 2B mutations in asymptomatic patients, and let to perform prophylactic thyroidectomy in children. RET mutations can also be responsible for MEN 2A syndrome (MTC, PC and hyperparathyroidism) or familial MTC (FMTC). The same RET gene is causative for Hirschsprung's disease (HSCR) in a variable percentage of patients and HSCR can be associated with MEN 2 [3–8]. The molecular analysis has given an important contribution to understand Ret protein functions and the correlation between genotype and phenotype in RET mutations carriers.
According to genetic diagnosis, RET mutation analysis can provide early diagnosis and treatment of such a rare syndrome as MEN 2B, and becomes part of an international protocol responding these requirements.
Neurocristopathies a unifying concept
Although the importance of the neural crest (NC) was first identified over a century ago, it has gained wide acceptance in vertebral development over the last 20 years . The neural crest cells contribute to the formation of structures through-out the body. Therefore, 1 out 3 human congenital malformations involves structures related to NC.
The Neurocristopathies Classification
Neoplastic and Non-Neoplastic
- Hirschsprung's disease
- Neurofibromatosis (Von Recklinghausen disease)
- Multiple endocrine neoplasia (MEN) type 1
- Mandibulofacial dysostosis
- Congenital Central Hypoventilation
- Neurocutaneous melanosis
- Familial neuroblastoma with Hirschprung' s disease
- CCHS + HSCR = Haddad syndrome
- Waardenburg + HSCR = Shah Waardenburg Syndrome
- Medullary thyroid carcinoma (MTC only)
- Noncromaffin paraganglioma
- Carcinoid tumors
Classification of MEN 2 and occurrence of MTC, and associated disorders (modified by Raue F et al, 2010
Cutaneus lichen amyloidosis, hirschsprung's Disease
Ganglioneuromatosis, marphanoid habitus, megacolon
Rare associated disorders
1) MEN 2A (Sipple's Syndrome) is characterized by MTC, pheochromocytoma (Pheo), and primary hyperplasia of the parathyroids (HPT).
2) MEN 2B is characterized by MTC, Pheo, mucosal ganglioneuromatos, and Marfanoid habitus. It is the rarest and most aggressive form of MEN type 2.
3) Familial MTC (FMTC) presents a low incidence of other associated disorders.
HPT is not a feature of MEN 2B. The MEN 2B has the highest mortality and morbidity. The high mortality reflects the early onset of MTC (generally during the first years of life). Unfortunately, at the time of the diagnosis an advanced MTC may be present.
Clinical Features of MEN 2B
The clinical features have to be well known, especially in case of sporadic MEN 2B where they represent the only possibility to obtain a early suspect of the syndrome.
In most of the cases they are the first unspecific manifestations. The patients can present alvus disorders characterized by constipation alternating with diarrhea already in the first weeks of life. These types of troubles are getting worse. If the MEN 2B patient has a contrast enema X-ray, his/her colon may show reduced caliber without haustra; and some diverticula may be present in descending colon and sigma, other patients show a megacolon. Intestinal mucosa will progressively develop multiple pseudo-polyps as result of multiple ganglioneuromas (GN)/ganglioneurofibromas (GNf) . Intestinal obstruction resulting from a colonic giant ganglioneuroma is rare [15, 16].
Mucosal Multiple Ganglioneuromas (GN) and Ganglioneurofibromas (GNf)
GN and GNf lesions are characterized by tumors from mucosal and submucosal layers with enormous hypertrophy of nerve fibers (GNf) among ENS. Submucosal ganglion cells are usually present in normal numbers or organized in giant ganglia (GN) and always associated with large trunks of ENS nervous fibers. Ectopic ganglia inside lamina propia mucosae are present in most of the cases.
Marfanoid Habitus with Skeletal Deformations and joint Laxity
The skeletal abnormalities are characterized by lordosis, kyphosis, kyphoscoliosis, joint laxity, talipes equinovarus and pectus deformity.
Inability to Cry Tears
In 2008, Brauckhoff et al reported that 86% of MEN 2B patients demonstrated inability to cry tears .
Palpable Cervical Tumor
Unfortunately, at time of diagnosis most of the sporadic MEN 2B patients present a palpable thyroid mass or thyroid nodules, all representing MTCs. As a matter of fact, MEN 2B is the least common (5-10% of all MEN), but the most aggressive form of MEN 2. Patients have a rapid onset of MTCs during the first year of life, and they have a more aggressive form of carcinoma with higher morbidity and mortality rates compared with patients with MEN 2A. Lymph node metastases are reported by the second year of life [4, 26].
Plasmatic Calcitonin and PGT
In all suspected MEN2B patients, plasmatic calcitonin (CT) in basal condition is measured. Values lower than 14 pg/ml and 19 pg/ml are considered normal in females and in males respectively . Pentagastrin test (PGT) can be performed by infusion of a 0, 5 μg/kg of body weight of pentagastrin contained in 5 mL of 0, 9% NaCl as a bolus. Plasmatic CT is measured before the infusion of the bolus, and after 1, 5 and 5 minutes. Stimulated CT values are considered normal when lower than 30 pg/ml in females and 110 pg/ml in males [27, 28].
PGT is handy used in older children or adult patients. Nevertheless it is not easy to perform this test in younger babies, because its normal range is not yet standardized in the first years of life and because during the first infancy it could not be completely without risks .
For these reasons the test is not very useful for early diagnosis.
Intestinal Ganglioneuromatosis and Enzymo-histochemical Pre-operative Diagnosis of MEN 2B
Enzymo-histochemical studies of MEN 2B intestinal innervation have to be performed by the Acetylcolinesterase activity (AChE) technique, as described by Karnovsky and Roots [29, 75, 4]. AChE staining is very useful, because the picture is pathognomonic. The AChE is evaluated on rectal suction biopsies, as well as in the histochemical screening of HRSC.
Genetic Analysis of RET Proto-oncogene in MEN type 2
According to literature data it is evident that MEN 2, unlike other inherited cancer syndromes associated with inactivation of tumor suppressor gene, results from activation or "gain-of-function" mutations of RET gene. A single activating mutation on one allele of the RET proto-oncogene is sufficient to induce neoplastic transformation .
Genetic analysis of the RET proto-oncogene, allows molecular diagnosis of different neurocristopathies. The analysis can be performed in MEN 2A and MEN 2B familial cases, in subjects presenting sporadic MTC, or affected by HSCR.
Activating mutations of RET seem to be of the order of 1: 500.000 in the general population . Exons 10, 11, 13, 14, 15 and 16 of the RET proto-oncogene are analyzed for the detection of point mutations. In MEN 2A/FMTC cases, the analysis is firstly conducted in exons 10 and 11 by DGGE and subsequently in the remaining exons, if alterations had not been previously identified [4, 8, 32, 33].
In 98% of classic MEN 2A families, germline mutations cluster to the extracellular cysteine-rich domain of the RET gene and involve single base pair substitutions in one of the five cysteine codons in exon 10 (609, 611, 618, 620) or 11 (634). The great majority of the mutation detected in MEN 2A are in codon 634, with C634R (Cysteine to arginine substitution). Rare mutations associated with MEN2A include those in exon 11 (insertion/duplications in codon 635, 637), 13 (codons 768, 790, 791), 14 (codon 804), and 15 (codon 891). The majority of FMTC kindreds also have germline mutations in the extracellular cysteine-rich region; however, in FMTC they are more evenly distributed among codon 618, 620 and 634. FMTC is also associated with non-cysteine mutations in the intracellular tyrosine kinase domain; this includes exon 13 (codons 768, 790, 791), 14 (codon 804) and 15 (codon 891). Recently it has been suggested that FMTC is part of MEN 2A spectrum, indicating variable allelic penetrance .
In MEN 2B patients, exon 16 is primarily screened since more than 95% of cases present the M918T mutation . A second point mutation at codon 883 has been found in 2%-3% of individual with MEN 2B [35, 36]. Tandem RET mutations of codons 805, 806 and 904 in cis configuration with the p.V804M mutation have also been reported in individuals with MEN 2B [37–39].
Finally, all HSCR patients were screened for mutations in exon 10, since some families presenting the association of HSCR and FMTC/MEN2A segregate one of the mutations affecting the cysteine residues in exon 10 .
DGGE analysis is performed as previously reported . Sequencing of the altered PCR products is directly performed using dye terminator chemistry (Dye Terminator Cycle Sequencing Kit - ABI Prism Perkin Elmer, Norwalk, CT, USA) following the user's manual instructions. Electrophoresis of the cycle-sequencing products is carried out in an ABI 377 Automated Sequencer (Applied Biosystems, Foster City, CA, USA) and results are analyzed through an appropriate software.
In MEN 2B and FMTC are generally seen mutations involving intracellular non-cysteine codons in the tyrosine kinase domain. These mutations alter either adenosine triphosphate binding (codons 768, 790, 791, 804 and 891) or the substrate recognition pocket of the catalytic core (codon 918) resulting in altered substrate specificity of the RET protein. These altered RET isoforms cause aberrant phosphorylation of the substrate and activation of RET signaling pathways that induce cellular transformation .
RET Mutations in Hirschsprung's Disease
Hirschusprung's disease is the commonest cause of intestinal obstruction in the early pediatric age group with a recognized recurrence risk of 4% for sibs of affected individuals in comparison with the general population incidence rate of 1/5000 live births with male to female ratio 4: 1. There is a remarkable association with other genetic diseases, including malformations and/or chromosomal anomalies that will be discussed successively in this chapter. Many genetic informations are obtained from animal models affected with colonic aganglionosis showing specific pattern of inheritance and genetic defects.
Sporadic occurrence accounts for 80-90% of HSCR cases with a variable expressivity (different length of aganglionic segments between patients), and an incomplete sex dependent penetrance (whether the individual shows a phenotype of his genotype or not). All these features of HSCR suggest a more complex pattern of inheritance (multifactorial) as well as the involvement of many genes (genetic heterogeneity)
Through segregation analysis on different sets of patients and their families, different forms of inheritance were suggested depending on the length of aganglionic segment. HSCR was classified as autosomal dominant with incomplete penetrance for long segment HSCR and autosomal recessive or multifactorial in short segments HSCR form [41, 42].
A first step in understanding the molecular basis of HSCR was the observation of a little girl who was affected by total colonic aganglionosis with de-novo interstitial deletion in chromosome 10 (46xx, del.10 q11.21-q21.2) . Further investigations allowed the reduction of this region into 200 kb which was the area of RET proto-oncogene . The molecular strategy started with the published cDNA sequence at that time and the exon-intron structure of this gene was reconstructed by using a PCR based approach [45–47]. The intronic sequences flanking the 5' and 3' ends of each one of the first 20 exons (which were known at that time) were used to design primers and to amplify each exon. The analysis was later subjected to Single Strand Conformational Polymorphism (SSCP), leding to the identification of different forms of mutations .
RET gene was found to be mutated in about 35% of sporadic cases and 49% of familial HSCR cases and in a higher percent in long HSCR than in short type (76% vs 32%) [17, 23]. RET mutations that lead to HSCR can occur throughout the 21 exons of the gene and at least 89 mutations have been identified, including nonsense mutations, missense mutations, small deletions, and insertions [49, 50]. On the other hand, mutations leading to MEN2A or FMTC-familial medullary thyroid carcinoma are point mutations localized in one of 5 cysteins of the extracellular domains and they are activating mutations unlike those causing HSCR [45–47]. HSCR mutations in RET gene lead to loss of function alleles and they are heterozygous in nature which suggests haploinsufficiency.
About 5-10% of patients show other mutations in other genes as Glial cell Lined Derived Neurotrophic Factor (GDNF), Neurturin (NTN), Endothelin3 (EDN3), Endothelin B Receptor (EDNRB), Endothelin Converting Enzyme 1 (ECE1), The Transcriptional factor SOX10, Smad Interacting protein-1 (SIP1) and PHOX2B gene [42, 50, 54–56].
RET is primarly expressed during embryonic life in the neural crest, urogenital precursors, adrenal medulla and thyroid and later on throughout postnatal life in central and peripheral nervous systems and the endocrine system .
Mutations in RET gene play an essential role in two common neurocristopathies: MEN2 (OMIM 171400 and 162300) an autosomal dominant disorder caused by activating mutations and HSCR(OMIM 142623) which is believed to be caused by loss of function mutations.
Although HSCR and MEN2 are usually observed in isolated cases and probably they result from different molecular and cellular mechanisms due to different mutation types, the identification of RET mutations (C618 and C620) in families that have both HSCR and MEN 2 (FMTC and MEN2A) was surprising. The underlying mechanism that leads to both diseases is unknown  and it has been reported in a number of families who have HSCR but carry the mutation leading to MEN2 . This may give clue about the peculiar molecular mechanisms of the previous diseases. In order to explain how the same mutations can produce such diverse phenotype, we may hypothesize that they are the results of mutations occurring in different periods of embryonic and postnatal life.
Another explanation for the complex inheritance pattern of HSCR and the low detection rate for RET mutations is the presence of several common polymorphisms of RET gene associated with HSCR causing variable risk. Specific RET haplotypes have been found to act as protective or predisposing factors or to modulate the severity of the disease [57, 52, 59, 58, 60–62]. A specific haplotype of a rare allele of Single Nucleotide Polymorphism (SNP) of exon 2 (A45A) has been strongly associated with HSCR while the haplotype of an allele in exon 14 SNP (S836s) has shown a low penetrant protective factor against the disease . Another recent study supports the existence of low penetrant variant of the RET gene lying within or close to the ACA allele, which is believed to have an effect on either RET transcription, splicing or function, and considered a susceptible allele causing HSCR .
Neuroblastoma and RET Proto-oncogene
The role of RET gene in neuroblastoma has been debated for several years. Indeed, RET is an essential gene for the development of NC the same tissue from which neuroblastoma origins. So, the possibility that RET gene is associated with neuroblastoma carcinogenesis has been investigated by several research groups. However, Hofstra et al and Peaston et al report no RET gene mutations in both sporadic and hereditary neuroblastoma; only one case of RET mutation associated with NME1 mutation has been reported by Leone et al [64–66]. It is interesting to note that no RET mutation has been observed in familial neuroblastoma although this malignancy onsets frequently in the first year of life indicating that the carcinogenesis process already starts during the embryonic life .
Experimental evidences indicate that abnormal RET gene expression may play a role in disturbing the physiological NC development and participate to the neuroblastoma cell formation. D'Alessio et al observed that RET expression induces neuroblastoma cells differentiation and more recently the same researchers demonstrated that TRKB oncogene, another gene involved in NC development, cooperate with RET to differentiate these cells [68, 69]. Several neuroblastoma cell lines express RET together with other tyrosine kinase receptors of the GDNF family (GFR-1, -2 and -3). Bachetti et al show that several transcription factors deregulate RET expression in neuroblastoma and Kurotsuchi et al report that DOK family genes influence the RET gene activity in this tumor [70, 71]. Finally, the role of RET in neuroblastoma seems to be strongly associated with the induction of neuroblastoma cell maturation by retinoic acid. Retinoic acid is a well known and potent inducer of terminal cell differentiation of neuroblastoma cells. Most of all neuroblastoma cell lines are sensitive to the retinoic acid activity and the acid has been also employed for the treatment of High-Risk neuroblastoma patients to induce terminal neuroblastoma cell differentiation after bone marrow depletion . Angrisano et al have shown that several and complex events such as modification of DNA methylation are associated with RET activity by retinoic acid . This observation should be taken in to account for the treatment of neuroblastoma cells by retinoic acid.
Early Diagnosis and Prophylactic Surgery in MEN 2B
Prohylactic total thyroidectomy is performed in gene mutation carriers in accordance with their potential risk . Genetic diagnostic screening for MEN 2A should include at least the cysteine-containing codons 10, 11, and 16, but also exon 13 and 14. It is now established that the risk groups are determined by the genotype and should be used to dictate timing of prophylactic surgery. Recommendations on the timing of prophylactic thyroidectomy and extent of surgery were presented at the International Multiple Endocrine Neoplasia Meeting in 2001. The risk was stratified into tree classes using genotype-phenotype correlations [17, 18]. Children with codon 883, 918, and 922 mutations have to be classified as level 3 (MEN 2B), with the highest risk of early and aggressive MTC. Total thyroidectomy with central node dissection is recommended for patients with these mutations by the age of 6 months. Children with RET codon 611, 618, 620, and 634 mutations (MEN 2A) have to be classified as level 2 or as having a high risk of MTC. Thyroidectomy with or without central node dissection is recommended for patients with these mutations before the age of 5 years. Children with RET codon 609, 768, 790, 791, 804, and 891 mutations have to be classified as level 1 with the lowest risk of MTC. Operation in level 1 class is recommended at the age of 10 years .
Immunohistochemical Post-operative Diagnosis in Resected Thyroids
Resected thyroids have to be weighed, measured, fixed in formalin and divided in three parts, namely right and left lobe, and hysthmus. Each part is divided by transverse serial sections into specimens, and embedded in toto. Histological sections are obtained from specimens embedded in paraffin, using the technique of semiserial sections. The sections obtained have to be stained alternatively with hematoxylin-eosin and histochemical reactions for tirocalcitonin (BioGenex, prediluited, policlonal) chromogranin A (BioGenex, prediluited, clone LK2H10) and tyroglobulin (BioGenex 1: 10, clone 2H11). For histochemical reactions, routine procedures for the antigen unmasking are used (treatment in microwave oven in citrate buffer, ph 6, 10 mM). Dako Envison Peroxidase is used as revelation system.
Patients underwent to total thyroidectomy show C cell hyperplasia with "in situ" MTC, or large nodules of MTC.
Multiple Endocrine Neoplasia type 2B is a complex neoplastic neurocristopathy. MEN 2B is the rarest and most aggressive form of MEN. Prognosis in patients with MEN 2B syndrome depends on early diagnosis and surgical treatment. According to literature data, MTC occurs in 100% of MEN 2B and is very aggressive . When it becomes clinically manifest, it can be too late for curative surgery. Metastases are present at surgery for clinical or biochemical evidence of MTC in 45% of MEN 2B patients .
In agreement with literature data, in our series of patients the first clinical signs of MEN 2B affected the gastroenteric system . These symptoms are associated with typical marphanoid facies and multiple ganglioneuromas. The marphanoid features are not easy to identify in the first years of life, and ganglioneuromas at that time may be evident, but can be found if searched carefully. Gastrointestinal symptoms of MEN 2B generally include constipation or stipsis alternating with diarrhoea. These signs generally appear very early and sometimes are present already at birth, but they rarely suggest the diagnosis of MEN 2B. In children with constipation or stipsis alternating with diarrhoea, the presence of ganglioneuromas on the tongue and oral mucosa should be investigated, as well as the typical facies of MEN 2B and the family history of MTC or PC. In suspected cases, rectal biopsy has to be performed . In both cases, the pathognomonic picture of MEN 2B was observed, namely: submucous plexus hyperplasia with giant ganglia (GN and GNf), submucous fibromatosis, and ectopic ganglia (Figure 4 and 5) . In our opinion, rectal biopsy should be performed at first, as it allows diagnosis at an early disease stage. RET analysis is fundamental to confirm the diagnosis, and has to be extended to relatives. All carriers of MEN 2B mutations should undergo total thyroidectomy. On the basis of our experience and of literature data, prophylactic thyroidectomy is justified within the first year of life in patients with genetic diagnosis of MEN 2B [76, 32, 26, 77, 78].
The presentation of MEN 2B with thyroid mass can occur in cases with delayed diagnosis. In these patients the neuromas, the typical facies and the gastrointestinal symptoms are usually present. In these patients the diagnosis must be confirmed as soon as possible, with rectal biopsy and molecular analysis, in order to perform a total thyroidectomy associated with limphadenectomy. Fine needle aspiration of the mass is not advisable, in our opinion, because the result does not change the treatment, which anyway is based on surgery.
In the pre-operative work up we include cervical sonography and measurement of biochemical MTC markers: CT and CEA, useful for the follow up . In case of thyroid mass, it is advisable to perform CT-scan, abdominal sonography and skeletal scintigraphy, in order to search for lymph node, hepatic or bone metastases.
Today, PGT has been replaced with molecular genetic analysis, which is much safer. Actually in pediatric patients PGT can be ill-tolerated and give false negative results. When positive, it can indicate the presence of carcinoma or C cell hyperplasia [79, 27]. For these reasons, in our opinion this test is no longer indicated in the diagnosis of MEN 2B, whereas evaluation of basal plasma calcitonin CT in MEN 2B patients can play a role in their follow up.
In MEN 2B molecular genetic diagnosis, exon 16 is primarily screened since more than 95% of cases present the M918T mutation [4, 32]. Finally, all HSCR patients were screened for mutations in exon 10, since some families presenting the association of HSCR and FMTC/MEN2A segregate one of the mutations affecting the cysteine residues in exon 10 . A second point mutation at codon 883 has been found in 2%-3% of individual with MEN 2B [35, 36]. Tandem RET mutations of codons 805, 806 and 904 in cis configuration with the p.V804M mutation have also been reported in individuals with MEN 2B [37–39].
After the genetic diagnosis of a patient affected with MEN 2B, every member of his/her family have to be screened for the M918T mutation. Even in the presence of family history of MEN 2B, genetic analysis should always be associated with enzymo-histochemical study on rectal biopsy, as it allows rapid diagnosis (1 day).
An interesting aspect is the association of MEN 2 with HSCR. It is well known that RET mutations can be causative for both HSCR and MEN 2 . In particular, in MEN 2A patients the most frequent RET mutation (85%) affects codon 634 of exon 11, while in MEN 2B patients codon 918 of exon 16 is almost always involved. In HSCR, RET mutation can affect any portion of the gene. Interestingly, the most frequent mutations found in patients with the association of HSCR and MEN 2A/FMTC involve codons 609, 618 and 620 of exon 10 [82, 83, 33, 45].
In HSCR patients, molecular analysis of standard MEN 2A/FMTC mutations is therefore recommended to identify a subpopulation of patients carrying mutations with potential oncologic risk.
The Ret protein is a tyrosine kinase receptor, that plays an important role in the activation of signalling pathways, through the phosphorylation of key tyrosine residues, in response to different ligands. In MEN 2A and MEN 2B, gain of function RET mutations result in the constitutive activation of the tyrosine kinase receptor, with subsequent phosphorylation and overtrasmission of the signal by different downstream pathways. The latter can be specifically activated by the different mutations, which therefore result in a large spectrum of possible phenotypes (MEN 2A, MEN 2B, FMTC, with different degrees of penetrance and expressivity). On the contrary, RET inactivating mutations are associated with HSCR. Loss of function mutations result in a reduction of the amount of functional Ret protein on the cell surface. Mutations found in patients with HSCR and MEN 2 association are able to activate the signalling pathways, like in isolated MEN 2, but the mutated isoform is unable to translocate to the cell surface. The result of activation in the thyroid and adrenal glands is tumorigenesis, while the decrease of functional protein on the cell surface causes HSCR phenotype .
In agreement with literature data, we believe that central compartment cervical lymphadenectomy should be performed during thyroidectomy for MEN 2B . Homolateral lymph node exploration (2 compartments) has to be performed in cases with macroscopic evidence of carcinoma at surgery, and bilateral lymphadenectomy (3 compartments) is necessary in the presence of evident lymph node metastases. If mediastinal lymph nodes are metastatic according to CT-scan, limphadenectomy has to be extended to the mediastinum (4 compartments) .
Despite autotransplantation of parathyroid glands in the forearm is usually performed, in pediatric patients we prefer to preserve them in their primary site, in order to avoid traumas and mechanical insults, that are frequent in childhood upper limbs [76, 26].
MEN 2B patients have to be followed year by year with measurement of CEA and CT, markers of possible MTC relapse (more strictly in the first year after surgery). While urinary metanephrines and fractionated catecholamines (epinephrine, norepinephrine, dopamine) are useful to identify possible development of PC.
In conclusion, early diagnosis and treatment of patients with MEN 2B are essential to their survival. The rarity of this syndrome can cause delayed diagnosis. MEN 2B is characterized by early clinical signs as nonspecific alvus disorders and, later, development of the typical facies and presence of ganglioneuromas. These signs, that precede tumor development, should suggest the diagnosis, which is based on rectal biopsy and genetic analysis. The protocol and diagnostic algorithm of MEN 2B that we propose (see Additional file 1) seems to offer the best life expectancy to patients affected by MEN 2B syndrome . Moreover, recent advances into the mechanisms of RET proto-oncogene signaling and pathways of RET signal transduction in the development of MEN 2 and MTC will allow new treatment possibilities.
Authors thank Silvia De Luca for editing the manuscript.
- Sipple JH: "The association of pheochromocytoma with carcinoma of the thyroid gland". American Journal of Medicine. 1961, 31: 163-166. 10.1016/0002-9343(61)90234-0.View ArticleGoogle Scholar
- Ihara M, Yamashita T, Okamoto T: "A nationwide clinical survey of patients with multiple endocrine neoplasia type 2 and familial medullary carcinoma in Japan". Japanese Journal Clinical Oncology. 1997, 27: 128-134. 10.1093/jjco/27.3.128.View ArticleGoogle Scholar
- Martucciello G, Ceccherini I, Lerone M: " Pathogenesis of Hirschsprung's disease". Journal of Pediatric Surgery. 2000, 35: 1017-1025. 10.1053/jpsu.2000.7763.View ArticlePubMedGoogle Scholar
- Romeo G, Ronchetto P, Lou Y: "Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirscsprung's disease". Nature. 1994, 367: 377-378. 10.1038/367377a0.View ArticlePubMedGoogle Scholar
- Martucciello G, Luinetti O, Romano P, Magrini U: "Molecular biology, basic research and diagnosis of Hirshsprung's disease". Pathologe. 2007, 28 (2): 119-124. 10.1007/s00292-007-0897-7.View ArticlePubMedGoogle Scholar
- Martucciello G: "Hirschsprung's disease, one of the most difficult diagnoses in pediatric surgery: a review of the problems from clinical practice to the bench". European Journal of Pediatric Surgery. 2008, 18 (3): 140-149. 10.1055/s-2008-1038625.View ArticlePubMedGoogle Scholar
- Seri M, Yin L, Barone V: "Detection of Ret mutations in higher among long segment than short segment Hirschsprung patient". Human Mutation. 1997, 9: 243-249. 10.1002/(SICI)1098-1004(1997)9:3<243::AID-HUMU5>3.0.CO;2-8.View ArticlePubMedGoogle Scholar
- Romeo G, Ceccherini I, Celli J: "Association of multiple endocrine neoplasia type 2 and Hirschsprung disease". Journal of Internal Medicine. 1998, 243: 515-520. 10.1046/j.1365-2796.1998.00332.x.View ArticlePubMedGoogle Scholar
- Molenaar JC, Brooks A, Meijers C: "Neurocristopathies. From basic science to clinical practice", Gaslini. 1998, 30: 105-110.Google Scholar
- Martucciello G: "Hirschsprung's disease as a neurochristopathy". Pediatric Surgery International. 1997, 12: 2-10.View ArticlePubMedGoogle Scholar
- Bolande RP: "The neurocristopathies. a unifying concept of disease arising in neural crest maldevelopment", Human Pathology. 1974, 5: 409-429.Google Scholar
- Bronner-Fraser M: "Segregation of cell lineage in the neural crest". Current Opinion Genetic Development. 1993, 3: 641-647. 10.1016/0959-437X(93)90101-T.View ArticleGoogle Scholar
- Morre SW, Zaahl MG: "Multiple endocrine neoplasia syndromes. children, Hirschsprung'disease and RET", Pediatric Surgery International. 2008, 24: 521-520.View ArticleGoogle Scholar
- Raue F, Franke-Raue K: "Update multiple endocrine neoplasia type 2". Familial Cancer. 2010, 9: 449-457. 10.1007/s10689-010-9320-2.View ArticlePubMedGoogle Scholar
- Shocket E, Teloh HA: "Aganglionic megacolon, phaeochromocytoma, megaloureter and neurofibromatosis". American Journal of Diseases of Children. 94: 185-191.Google Scholar
- Moore SW: "Neurocristopathies and particular associations with Hirscsprung's disease". "Hirschsprung's disease and allied disorders" Third edition. Edited by Springer. Holschneider, Puri Eds. 2008, 18: 243-266.Google Scholar
- Brandi ML, Gagel RF, Angeli A: "Guidelines for diagnosis and therapy of MEN type 1 and type 2". The Journal of Clinical Endocrinology and Metabolism. 2001, 86: 5658-5671. 10.1210/jc.86.12.5658.View ArticlePubMedGoogle Scholar
- Engiz O, Ocal G, Siklar Z: "Early prophylactic thyroidectomy for Ret mutation-positive MEN 2B". Japan Pediatric Society. 2007, 590-593.Google Scholar
- Camacho CP, Hoff AO, Linsdey SC: " Early diagnosis of Multiple Endocrine Neoplasia type 2B: a challenge for physicians". Arq Bras Endocrinol Metab. 2008, 52/8: 1393-1398.View ArticleGoogle Scholar
- Morrison PJ, Nevin NC: "Multiple Endorine neoplasia type 2B (mucosal neuroma syndrome. Wagenmann-Froboese syndrome", Journal of Medical Genetics. 1996, 33: 779-782.View ArticlePubMedGoogle Scholar
- Sallai A, Hosszù E, Gergics P: "Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. presentation of two unrelated cases", European Journal of Pediatrics. 2008, 167: 441-446.View ArticlePubMedGoogle Scholar
- Wray CJ, Rich TA, Waguespack SG: "Failure to recognize multiple endocrine neoplasia 2B: more common than we think?". Annals of Surgical Oncology. 2007, 15 (1): 293-301.View ArticlePubMedGoogle Scholar
- Lee NC, Norton JA: "Multiple endocrine neoplasia type 2B-genetic basis and clinical expression". Surgical Oncology. 2000, 9: 111-118. 10.1016/S0960-7404(00)00038-4.View ArticlePubMedGoogle Scholar
- Lee MJ, Chung KH, Park JS: "Multiple endocrine neoplasia type 2B: early diagnosis by multiple mucosal neuroma and its DNA analysis". Annals of Dermatology vol 22. 2010, 4: 452-455.View ArticleGoogle Scholar
- Brauckhoff M, Machens A, Hess S: "Premonitory symptoms preceding metastatic medullary thyroid cancer in MEN 2B: an exploratory analysis". Surgery. 2008, 144: 1044-1051. 10.1016/j.surg.2008.08.028.View ArticlePubMedGoogle Scholar
- Skinner MA, de Benedetti MK, Moley JF: "Medullary Thyroid Carcinoma in Children With Multiple Endocrine Neoplasia Types 2A and 2B". Journal of Pediatric Surgery. 1996, 31: 177-182. 10.1016/S0022-3468(96)90343-7.View ArticlePubMedGoogle Scholar
- Heshmati HM, Gharib H, van Heerden JA: "Advances and controversies in the diagnosis and management of Medullary Thyroid Carcinoma". American Journal of Medicine. 1997, 103: 60-69. 10.1016/S0002-9343(97)00024-7.View ArticlePubMedGoogle Scholar
- Telenius-Berg M, Almqvist S, Berg B: "Screening for medullary carcinoma of the thyroid in families with Sipple's syndrome: evaluation of new stimulation tests". European Journal of Clinical Investigation. 1997, 7: 7-16.View ArticleGoogle Scholar
- Karnovsky MJ, Roots L: "A direct-coloring thiocholine method for cholinesterase". Journal of Hisochemestry and Cytochemestry. 1964, 12: 219-221. 10.1177/12.3.219.View ArticleGoogle Scholar
- Mukherjee S, Zakalik D: "RET codon 804 mutations in multiple endocrine neoplasia 2: genotype-phenotype correlations and implications in clinical management". Clinical Genetics. 2011, 79: 1-16. 10.1111/j.1399-0004.2010.01453.x.View ArticlePubMedGoogle Scholar
- Russo A, Zanna I, Tubiolo C: "Hereditary common cancers: molecular and clinical genetics". Anticancer Research. 2000, 20: 4841-4851.PubMedGoogle Scholar
- O'Riordain DS, O'Brien T, Crotti TB: "Multiple endocrine neoplasia type 2B: more than an endocrine disorder". Surgery. 1995, 118: 936-942. 10.1016/S0039-6060(05)80097-2.View ArticlePubMedGoogle Scholar
- Ponder J: "The phenotype associated with RET mutations in the multiple endocrine neoplasia type 2 syndrome". Cancer Research. 1999, 59S: 1736-1742.Google Scholar
- Hansford JR, Mulligan LM: "Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis". Journal of Medical Genetics. 2000, 37: 817-27. 10.1136/jmg.37.11.817.PubMed CentralView ArticlePubMedGoogle Scholar
- Gimm O, Marsh DJ, Andrew SD, Frilling A: "Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation". The Journal of Clinical Endocrinology and Metabolism. 1997, 82: 3902-3904. 10.1210/jc.82.11.3902.View ArticlePubMedGoogle Scholar
- Smith DP, Houghton C, Ponder BA: "Germiline mutation of RET codon 883 in two cases of de novo MEN 2B". Oncogene. 1997, 15: 1213-1217. 10.1038/sj.onc.1201481.View ArticlePubMedGoogle Scholar
- Miyauchi A, Futami H, Hai N: "Two germline missense mutations at codons 804 and 806 of the RET proto- oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without codon 918 mutation". Japanese Journal of Cancer Research. 1999, 90: 1-5. 10.1111/j.1349-7006.1999.tb00658.x.View ArticlePubMedGoogle Scholar
- Cranston AN, Carniti C, Oakhill K: "RET is constitutively activated by novel tandem mutations that alter the active site resulting in multiple endocrine neoplasia type 2B". Cancer Research. 2006, 66: 10179-10187. 10.1158/0008-5472.CAN-06-0884.View ArticlePubMedGoogle Scholar
- Menko FH, van der Luijt RB, de Valk IA: "Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918". The Journal of Clinical Endocrinology and Metabolism. 2002, 87: 393-397. 10.1210/jc.87.1.393.View ArticlePubMedGoogle Scholar
- Hofstra RM, Wu Y, Stulp RP: "RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems". Human Mutation. 2000, 15: 418-29. 10.1002/(SICI)1098-1004(200005)15:5<418::AID-HUMU3>3.0.CO;2-2.View ArticlePubMedGoogle Scholar
- Garver KL, Law JC, Garver B: "Hirschsprung disease: a genetic study". Clinical Genetics. 1985, 28 (6): 503-508.View ArticlePubMedGoogle Scholar
- Badner JA, Sieber WK, Garver KL: "A genetic study of Hirschsprung disease". American Journal of Human Genetics. 1990, 46: 568-580.PubMed CentralPubMedGoogle Scholar
- Martucciello G, Bicocchi MP, Dodero P: "Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10". Pediatric Surgery. 1992, 7: 308-310.Google Scholar
- Ceccherini I, Yin L, Pasini B: "Close linkage with RET protoncogene and deletion mutation in autosomal dominant Hirschsprung disease". Human Molecular Genetics. 1993, 2, 11: 1803-1808.Google Scholar
- Takahashi M, Burma Y, Iwamoto T: "Cloning and expression of the RET protoncogene encoding a tyrosine kinase with two potential transmembrane domains". Oncogene. 1988, 3: 571-578.PubMedGoogle Scholar
- Takahashi M, Burma Y, Hiai H: "Isolation of the RET protoncogene cDNA with an aminoterminal signal sequence". Oncogene. 1989, 4: 805-806.PubMedGoogle Scholar
- Ceccherini I, Bocciardi R, Yin L: "Exon structure and flanking intronic sequences of the human RET proto-oncogene". Biochemical and Biophysical Research Communication. 1993, 196: 1288-1295. 10.1006/bbrc.1993.2392.View ArticleGoogle Scholar
- Ceccherini I, Hofstra RM, Lou Y: " DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the RET proto-oncogene". Oncogene. 1994, 9: 3025-3029.PubMedGoogle Scholar
- Meijers JH, van der Sanden MP, Tibboel D: "Colonization characteristics of enteric neural crest cells: embryological aspects of Hirschsprung's disease". Journal of Pediatric Surgery. 1992, 27 (7): 811-814. 10.1016/0022-3468(92)90371-D.View ArticlePubMedGoogle Scholar
- Chakravarti A, Lyonnet S: "Hirschsprung disease". The Metabolic and Molecular Bases of Inherited Disease. Edited by: Scriver Cr, Beaudet Al, Valle D, Sly W. 2000, McGrw-Hill, New York, 8Google Scholar
- Ito S, Iwashita T, Asai N: "Biological properties of Ret with cysteine mutations correlate with multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma and Hirschsprung's disease phenotype". Cancer Research. 1997, 57 (14): 2870-2872.PubMedGoogle Scholar
- Borrego S, Saez ME, Ruiz A: "Specific polymorphism in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression". Journal of Medical Genetics. 1999, 36: 771-774.PubMed CentralView ArticlePubMedGoogle Scholar
- Fitze G, Schreiber M, Kuhlisch E: "Association of RET protoncogene codon 45 polymorphism with Hirschsprung disease". American Journal of Human Genetics. 1999, 65: 1469-1473. 10.1086/302618.PubMed CentralView ArticlePubMedGoogle Scholar
- Bolk S, Pelet A, Hofstra RM: "A humans model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the Ret gene and a new 9q31 locus". Proceedings of the National Academy of Science of The United States of America. 2000, 97 (1): 268-273. 10.1073/pnas.97.1.268.View ArticleGoogle Scholar
- Gabriel SB, Salomon R, Pelet A: " Segregation at three loci explains familial and population risk in Hirschsprung disease". Nature Genetics. 2002, 31: 89-93.PubMedGoogle Scholar
- Amiel J, Lyonnet S: "Hirschsprung disease. associated syndromes, and genetics: a review", Journal of Medical Genetics. 2001, 38: 729-739.PubMedGoogle Scholar
- Carrasquillo MM, McCallion AS, Puffenberg EG: "Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease". Nature Genetics. 2002, 32: 237-244. 10.1038/ng998.View ArticlePubMedGoogle Scholar
- Ponder LM, Ponder BA: "Genetic basis of endocrine disease multiple endocrine neoplasia type 2". The Journal of Clinical Endocrinology and Metabolism. 1995, 80: 1989-1995. 10.1210/jc.80.7.1989.PubMedGoogle Scholar
- Borrego S, Ruiz A, Saez ME: "RET genotypes comprising specific haplotypes of polimorphic variants predispose to isolated Hirschsprung disease". Journal of Medical Genetics. 2000, 37: 572-578. 10.1136/jmg.37.8.572.PubMed CentralView ArticlePubMedGoogle Scholar
- Griseri P, Sancandi M, Patrone G: " A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease". European Journal of Human Genetics. 2000, 8: 721-724. 10.1038/sj.ejhg.5200521.View ArticlePubMedGoogle Scholar
- Fitze G, Cramer J, Ziegler A: "Association between c135G/A genotype and RET protoncogene germiline mutations and phenotype of Hirschsprung's disease". Lancet. 2002, 6: 1200-1205.View ArticleGoogle Scholar
- Griseri P, Pesce B, Patrone G: "A rare haplotype of the RET proto-oncogene is a risk-modifying allele in Hirschsprung disease". American Journal of Human Genetics. 2002, 71: 969-974. 10.1086/342774.PubMed CentralView ArticlePubMedGoogle Scholar
- Ceccherini I, Sancandi M, Griseri P: "Single nucleotide polymorphic allele in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's disease". Journal of Medical Genetics. 2003, 49: 714-718.Google Scholar
- Hofstra RM, Chang NC, Hansen C: "No mutations found by RET mutation scanning in sporadic and hereditary neuroblastoma". Human Genetics. 1996, 97: 362-364. 10.1007/BF02185773.View ArticlePubMedGoogle Scholar
- Peaston AE, Camacho ML, Norris MD: "Absence of MEN2A- or 2B-type RET mutations in primary neuroblastoma tumour tissue". Molecular and Cellular Probes. 1998, 12: 239-242. 10.1006/mcpr.1998.0181.View ArticlePubMedGoogle Scholar
- Leone A, Seeger RC, Hong CM: "Evidence for nm23 RNA overexpression, DNA amplification and mutation in aggressive childhood neuroblastomas". Oncogene. 1993, 8: 855-865.PubMedGoogle Scholar
- Maris J, Tonini GP: "Genetics of familial neuroblastoma". Neuroblastoma. Edited by: Brodeur GM, Sawada T, Tsuschida Y, Vote PA. 2000, Elsevier, Amsterdam, 125-135.Google Scholar
- D'Alessio A, De Vita G, Calì G: "Expression of the RET oncogene induces differentiation of SK-N-BE neuroblastoma cells". Cell Growth and Differentiation. 1995, 6 (11): 1387-1394.PubMedGoogle Scholar
- Esposito CL, D'Alessio A, de Franciscis V: "A cross-talk between TrkB and Ret tyrosine kinases receptors mediates neuroblastoma cells differentiation". Public Library of Science One. 2008, 20;3 (2): e1643-Google Scholar
- Bachetti T, Borghini S, Ravazzolo R: "An in vitro approach to test the possible role of candidate factors in the transcriptional regulation of the RET proto-oncogene". Gene Expression Pattern. 2005, 12 (3): 137-149.View ArticleGoogle Scholar
- Kurotsuchi A, Murakumo Y, Jijiwa M: "Analysis of DOK-6 function indownstream signaling of RET in human neuroblastoma cells". Cancer Science. 2010, 101 (5): 1147-1155. 10.1111/j.1349-7006.2010.01520.x.View ArticlePubMedGoogle Scholar
- Matthay KK, Tan JC, Villablanca JG: "Phase I dose escalation of iodine-131-metaiodobenzylguanidine with myeloablative chemotherapy and autologous stem-cell transplantation in refractory neuroblastoma: a new approaches to Neuroblastoma". Therapy Consortium Study, Journal of Clinical Oncology 20. 2006, 24 (3): 500-506.View ArticleGoogle Scholar
- Angrisano T, Sacchetti S, Natale F: "Chromatin and DNA methylation dynamics during retinoic acid-induced RET gene transcriptional activation in neuroblastoma cells". Nucleic Acids Research. 2011, 39 (6): 1993-2006. 10.1093/nar/gkq864.PubMed CentralView ArticlePubMedGoogle Scholar
- Dralle H, Scheumann GFW, Kotzerke J: "Surgical management of MEN 2. Recent Results" Cancer Research. 1992, 125: 167-195. 10.1007/978-3-642-84749-3_9.View ArticleGoogle Scholar
- Martucciello G, Caffarena PE, Lerone M: "Neuronal Intestinal Displasia: clinical Experience in Italian Patients". European Journal of Pediatric Surgery. 1994, 4: 287-292. 10.1055/s-2008-1066119.View ArticlePubMedGoogle Scholar
- Iler MA, King RD, Ginn-Pease ME: "Multiple endocrine neoplasia type 2A: a 25-year review". Journal of Pediatric Surgery. 1999, 34: 92-97. 10.1016/S0022-3468(99)90236-1.View ArticlePubMedGoogle Scholar
- Van Heurn LW, Svhaap C, Sie G: "Predictive DNA testing for multiple endocrine neoplasia 2: a therapeutic challenge of prophylactic thyroidectomy in very young children". Journal of Pediatric Surgery. 1999, 34: 568-571. 10.1016/S0022-3468(99)90075-1.View ArticlePubMedGoogle Scholar
- Wells SA, Chi DD, Toshima K: "Predictive DNA testing and prophylactic thyroidectomy in patients at risk for Multiple Endocrine Neoplasia type 2A". Annals of Surgery. 1994, 220: 237-250. 10.1097/00000658-199409000-00002.PubMed CentralView ArticlePubMedGoogle Scholar
- Decker RA, Peacock ML, Borst MJ, Sweet J: "Progress in genetic screening of multiple endocrine neoplasia type 2A: Is calcitonin testing obsolete?". Surgery. 1995, 118: 257-264. 10.1016/S0039-6060(05)80332-0.View ArticlePubMedGoogle Scholar
- Decker RA, Peacock ML, Watson P: " Hirschsprung disease in MEN2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation". Human Molecular Genetics. 1998, 7: 129-134. 10.1093/hmg/7.1.129.View ArticlePubMedGoogle Scholar
- Dralle H, Scheumann GFW, Kotzerke J: "Surgical management of MEN 2". Recent Results Cancer Research. 1992, 125: 167-195. 10.1007/978-3-642-84749-3_9.View ArticleGoogle Scholar
- Borst MJ, Van Camp JM, Peacock ML: "Mutational anlysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease". Surgery. 1995, 117: 386-391. 10.1016/S0039-6060(05)80057-1.View ArticlePubMedGoogle Scholar
- Eng C, Clayton D, Schuffenecker I: "The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2". Journal of American Medical Association. 1996, 276: 1575-1579. 10.1001/jama.1996.03540190047028.View ArticleGoogle Scholar
- Torre M, Martucciello G, Ceccherini I: "Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patients". Pediatric Surgery International. 2002, 18: 378-383. 10.1007/s00383-002-0824-1.View ArticlePubMedGoogle Scholar
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