Literature DB >> 11981210

Gastrointestinal manifestations of multiple endocrine neoplasia type 2.

Mark S Cohen1, John E Phay, Charlotte Albinson, Mary K DeBenedetti, Michael A Skinner, Terry C Lairmore, Gerard M Doherty, Dennis M Balfe, Samuel A Wells, Jeffrey F Moley.   

Abstract

OBJECTIVE: To determine the clinical features, natural history, and role of surgery for gastrointestinal manifestations of the multiple endocrine neoplasia type 2 (MEN 2) syndromes. SUMMARY BACKGROUND DATA: The MEN 2 syndromes are characterized by medullary thyroid carcinoma and other endocrinopathies. In addition, some patients with MEN 2A develop Hirschsprung's disease (HD), and all patients with MEN 2B have intestinal neuromas and megacolon that can cause significant gastrointestinal problems.
METHODS: From 83 families with MEN 2A, eight patients with HD were identified (MEN 2A-HD). These and all patients with MEN 2B followed at the authors' institution (n = 53) were sent questionnaires to describe the onset and type of gastrointestinal symptoms and treatment they had before the diagnosis of MEN 2. Records of all patients responding were reviewed, including radiographic imaging, histology, surgical records, and genetic testing.
RESULTS: Thirty-six of the 61 patients (59%) responded (MEN 2A = 8, MEN 2B = 28) to the questionnaires. All patients with MEN 2A-HD were operated on for HD 2 to 63 years before being diagnosed with MEN 2. All patients responding were underweight as infants and had symptoms of abdominal pain, distention, and constipation. Eighty-eight percent had hematochezia, 63% had emesis, and 33% had intermittent diarrhea before surgery. All patients with MEN 2A-HD had rectal biopsies with a diverting colostomy as the initial surgical procedure. This was followed by a colostomy takedown and pull-through procedure at a later interval. Ninety-three percent of patients with MEN 2B had gastrointestinal symptoms 1 to 24 years before the diagnosis of MEN 2. Symptoms included flatulence (86%), abdominal distention or being underweight as a child (64%), abdominal pain (54%), constipation or diarrhea (43%), difficulty swallowing (39%), and vomiting (14%). Seventy-one percent of patients with MEN-2B with gastrointestinal symptoms had radiographic imaging, 32% were admitted to the hospital, and 29% underwent surgery.
CONCLUSIONS: Patients with MEN 2A-HD had a typical HD presentation and always required surgery. Patients with MEN 2B have significant gastrointestinal symptoms, but less than a third had surgical intervention. Understanding the clinical course and differences in these patients will improve clinical management.

Entities:  

Mesh:

Year:  2002        PMID: 11981210      PMCID: PMC1422490          DOI: 10.1097/00000658-200205000-00006

Source DB:  PubMed          Journal:  Ann Surg        ISSN: 0003-4932            Impact factor:   12.969


  17 in total

1.  Hirschsprung's disease in a family with multiple endocrine neoplasia type 2.

Authors:  M Verdy; A M Weber; C C Roy; C L Morin; M Cadotte; P Brochu
Journal:  J Pediatr Gastroenterol Nutr       Date:  1982       Impact factor: 2.839

2.  Multiple endocrine neoplasia (MEN) syndrome type IIB: gastrointestinal manifestations.

Authors:  T C Demos; J Blonder; W L Schey; S S Braithwaite; P L Goldstein
Journal:  AJR Am J Roentgenol       Date:  1983-01       Impact factor: 3.959

3.  Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease.

Authors:  M J Borst; J M VanCamp; M L Peacock; R A Decker
Journal:  Surgery       Date:  1995-04       Impact factor: 3.982

4.  Association of multiple endocrine neoplasia type 2 and Hirschsprung disease.

Authors:  G Romeo; I Ceccherini; J Celli; M Priolo; N Betsos; G Bonardi; M Seri; L Yin; M Lerone; V Jasonni; G Martucciello
Journal:  J Intern Med       Date:  1998-06       Impact factor: 8.989

5.  Alimentary-tract ganglioneuromatosis. A major component of the syndrome of multiple endocrine neoplasia, type 2b.

Authors:  J A Carney; V L Go; G W Sizemore; A B Hayles
Journal:  N Engl J Med       Date:  1976-12-02       Impact factor: 91.245

6.  Gastrointestinal manifestations of Sipple syndrome in children.

Authors:  A H Khan; J G Desjardins; S Youssef; H Grégoire; E Seidman
Journal:  J Pediatr Surg       Date:  1987-08       Impact factor: 2.545

7.  Mutations of the RET proto-oncogene in Hirschsprung's disease.

Authors:  P Edery; S Lyonnet; L M Mulligan; A Pelet; E Dow; L Abel; S Holder; C Nihoul-Fékété; B A Ponder; A Munnich
Journal:  Nature       Date:  1994-01-27       Impact factor: 49.962

8.  Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease.

Authors:  G Romeo; P Ronchetto; Y Luo; V Barone; M Seri; I Ceccherini; B Pasini; R Bocciardi; M Lerone; H Kääriäinen
Journal:  Nature       Date:  1994-01-27       Impact factor: 49.962

9.  Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.

Authors:  L M Mulligan; C Eng; T Attié; S Lyonnet; D J Marsh; V J Hyland; B G Robinson; A Frilling; C Verellen-Dumoulin; A Safar
Journal:  Hum Mol Genet       Date:  1994-12       Impact factor: 6.150

10.  Multiple endocrine neoplasia type II B with symptoms suggesting Hirschsprung's disease: a case report.

Authors:  S M Mahaffey; L W Martin; A J McAdams; F C Ryckman; M Torres
Journal:  J Pediatr Surg       Date:  1990-01       Impact factor: 2.545

View more
  23 in total

1.  Giant inguinoscrotal hernia.

Authors:  U M Monestiroli; A Bondurri; F Gandini; G Lenna; S Vellini; P Danelli
Journal:  Tech Coloproctol       Date:  2007-09       Impact factor: 3.781

Review 2.  Classification and diagnostic criteria of variants of Hirschsprung's disease.

Authors:  Florian Friedmacher; Prem Puri
Journal:  Pediatr Surg Int       Date:  2013-09       Impact factor: 1.827

Review 3.  Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes.

Authors:  Robert O Heuckeroth
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2018-01-04       Impact factor: 46.802

Review 4.  Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.

Authors:  Samuel A Wells; Sylvia L Asa; Henning Dralle; Rossella Elisei; Douglas B Evans; Robert F Gagel; Nancy Lee; Andreas Machens; Jeffrey F Moley; Furio Pacini; Friedhelm Raue; Karin Frank-Raue; Bruce Robinson; M Sara Rosenthal; Massimo Santoro; Martin Schlumberger; Manisha Shah; Steven G Waguespack
Journal:  Thyroid       Date:  2015-06       Impact factor: 6.568

5.  Characteristics of chronic megacolon among patients diagnosed with multiple endocrine neoplasia type 2B.

Authors:  Denys Gibbons; Michael Camilleri; Alfred D Nelson; Deborah Eckert
Journal:  United European Gastroenterol J       Date:  2015-10-13       Impact factor: 4.623

6.  Missed Diagnosis of Multiple Endocrine Neoplasia Type 2 B.

Authors:  A Gundgurthi; M K Dutta; R Pakhetra; M K Garg
Journal:  Med J Armed Forces India       Date:  2011-07-21

Review 7.  Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.

Authors:  Jonathan D Wasserman; Gail E Tomlinson; Harriet Druker; Junne Kamihara; Wendy K Kohlmann; Christian P Kratz; Katherine L Nathanson; Kristian W Pajtler; Andreu Parareda; Surya P Rednam; Lisa J States; Anita Villani; Michael F Walsh; Kristin Zelley; Joshua D Schiffman
Journal:  Clin Cancer Res       Date:  2017-07-01       Impact factor: 12.531

8.  Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases.

Authors:  Agnes Sallai; Eva Hosszú; Péter Gergics; Károly Rácz; György Fekete
Journal:  Eur J Pediatr       Date:  2007-06-19       Impact factor: 3.183

9.  Isolated intestinal neuronal dysplasia Type B (IND-B) in Japan: results from a nationwide survey.

Authors:  T Taguchi; H Kobayashi; Y Kanamori; O Segawa; A Yamataka; M Sugiyama; T Iwanaka; N Shimojima; T Kuroda; A Nakazawa; Y Oda; K Miyoshi; S Ieiri
Journal:  Pediatr Surg Int       Date:  2014-07-23       Impact factor: 1.827

Review 10.  Multiple Endocrine Neoplasia: A Genetically Diverse Group of Familial Tumor Syndromes.

Authors:  M Cristina Pacheco
Journal:  J Pediatr Genet       Date:  2016-03-09
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.