[Diagnostic and therapeutic difficulties in MEN 1 syndrome]

Endokrynol Pol. 2005 May-Jun;56(3):302-7.
[Article in Polish]

Abstract

MEN 1 syndrome (Multiple Endocrine Neoplasia type 1) is a rare endocrine disorder characterized by the association of tumors in several endocrine glands, mainly in parathyroids, gut and pituitary. At our institution in the years 1982-2004 we have followed 26 patients with MEN 1 syndrome belonging to 19 families. The diagnosis of MEN 1 was based on Gubbio Consensus (JCEM 86: 5658-5671, 2001). Mean age at the diagnosis of MEN 1 was 35 years. Primary hyperparathyroidism was the most frequent pathology, which was diagnosed in 25 of 26 patients (96%). Gut endocrine tumors were found in 20 patients (77%), while pituitary tumors in 18 (70%). Non-functioning gut tumors were most frequent (n=9), followed by insulinoma (n=7) and gastrinoma (n=4). Prolactinoma was the most frequent pituitary tumor found in 12 patients (67%). Three patients died during the observation period - all of them of generalized gut endocrine tumor (gastrinoma in 2 cases and foregut carcinoid in one case). The management of MEN 1 is not easy and careful analysis of clinical picture is necessary in each individual case. Several important observations can be made on the basis of own experience and the literature: 1. In each sporadic pathology, which may be a part of MEN 1, one should consider. the possibility of MEN 1. The individual MEN 1 abnormalities are often diagnosed after 40 and later 2. MEN 1 tumor are usually multiple thus necessitating a different therapeutic approach (more radical surgery) 3. The most valuable screening tests are: Ca++, PP, CgA and prolactin 4. Endoscopic ultrasound is the most specific method for the localization of pancreatic endocrine tumors. 5. The results of surgical treatment of MEN 1 tumors are worse than that of sporadic tumors. 6. Prognosis in MEN 1 is determined by the behaviour of gut neuroendocrine tumor 7. No genotype/phenotype correlation in MEN 1 syndrome was found so far. In summary, it should be underlined that MEN 1 syndrome is an endocrine disorder, in which early diagnosis and optimal treatment may significantly improve the prognosis.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Adult
  • Diagnosis, Differential
  • Female
  • Follow-Up Studies
  • Gastrinoma / diagnosis
  • Gastrinoma / therapy
  • Humans
  • Intestinal Neoplasms / diagnosis
  • Intestinal Neoplasms / therapy
  • Male
  • Middle Aged
  • Multiple Endocrine Neoplasia Type 1 / diagnosis*
  • Multiple Endocrine Neoplasia Type 1 / therapy*
  • Neoplasm Staging
  • Pancreatic Neoplasms / diagnosis
  • Pancreatic Neoplasms / therapy
  • Pituitary Neoplasms / diagnosis
  • Pituitary Neoplasms / therapy
  • Retrospective Studies
  • Risk Factors
  • Stomach Neoplasms / diagnosis
  • Stomach Neoplasms / therapy