Metodologia di editing immagini per analisi dati morfometrici dei primi stadi di sviluppo di Engraulis encrasicolus (Linnaeus, 1758)

Tra le più importanti risorse alieutiche di molte regioni del Mar Mediterraneo vi sonole acciughe (Engraulisencrasicolus, Linnaeus, 1758), piccoli pesci pelagici appartenenti alle famiglie degli Engraulidae. Dati IREPA del 2009, hanno di fatto reso noto che in Italia, la pesca di E. encrasicolusha rappresentano in media il 26% circa del pescato totale. Questa specie viene continuamente monitorata e grazie a tali programmi è stato evidenziato che vi sono delle fluttuazioni inter-annuali molto pronunciate (Cergoleet al., 2002; Cingolani, 2004), le cui cause possono essere molteplici, da fattori antropicicome l’elevato sforzo di pesca a fattori naturali (Borjia et al., 1996). Va però posta molta attenzione sulle dinamiche biologiche ed ambientali che influiscono sulla sopravvivenza dei primi stadi di vita di questa specie, che ricadendo sul successivo reclutamento, possono essere una delle cause fondamentali delle contrazioni e degli incrementi annuali dello stock adulto (Thikonova et al., 2000; James et al., 2003; Cuttitta et al., 2003, 2006).Lo studio delle fasi ittioplanctoniche e delle sue relazioni con l’ambiente e gli altri organismi, risulta quindi di primaria importanza nell’ambito delle conoscenze necessarie per il corretto sfruttamento delle risorse alieutiche.

Multiple endocrine neoplasia, the old and the new: a mini review

Multiple endocrine neoplasia syndromes have since been classified as types 1 and 2, each with specific phenotypic patterns. MEN1 is usually associated with pituitary, parathyroid and paraneoplastic neuroendocrine tumours. The hallmark of MEN2 is a very high lifetime risk of developing medullary thyroid carcinoma (MTC) more than 95% in untreated patients. Three clinical subtypesdMEN2A, MEN2B, and familial MTC (FMTC) have been defined based on the risk of pheochromocytoma, hyperparathyroidism, and the presence or absence of characteristic physical features). MEN2 occurs as a result of germline activating missense mutations of the RET (REarranged during Transfection) proto-oncogene. MEN2-associated mutations are almost always located in exons 10, 11, or 13 through 16. Strong genotype-phenotype correlations exist with respect to clinical subtype, age at onset, and aggressiveness of MTC in MEN2. These are used to determine the age at which prophylactic thyroidectomy should occur and whether screening for pheochromocytoma or hyperparathyroidism is necessary. Specific RET mutations can also impact management in patients presenting with apparently sporadic MTC. Therefore, genetic testing should be performed before surgical intervention in all patients diagnosed with MTC. Recently, Pellegata et al. have reported that germline mutations in CDKN1B can predispose to the development of multiple endocrine tumours in both rats and humans and this new MEN syndrome is named MENX and MEN4, respectively. CDKN1B. A recent report showed that in sporadic MTC, CDKN1B V109G polymorphism correlates with a more favorable disease progression than the wild-type allele and might be considered a new promising prognostic marker. New insights on MEN syndrome pathogenesis and related inherited endocrine disorders are of particular interest for an adequate surgical and therapeutic approach.