{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,5,27]],"date-time":"2023-05-27T04:04:33Z","timestamp":1685160273789},"reference-count":0,"publisher":"National Library of Serbia","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Acta chir iugo","ACTA CHIR IUG","ACTA CHIR IUGOSL"],"published-print":{"date-parts":[[2013]]},"abstract":"<jats:p>Neuroendocrine tumors (NET) are solid potentially malignant tumors originated\n   from the diffuse neuroendocrine system. They could origin in many organs,\n   with highest prevalence in lungs, small intestine and rectum. Characteristics\n   of NET are slow growth, non-specific clinical presentation causing diagnostic\n   problems. Thus, in majority of patients diagnosis is established in the\n   metastatic phase of the disease. Hopefully, there are new and very potent\n   treatment options capable to successfully control the disease. Clinical\n   presentation cause local tumor growth or para-neoplastic syndrome. Secretory\n   active tumors produce peptides or hormones causing different clinical\n   syndromes. In most cases NET cause carcinoid syndrome. It is often\n   misinterpreted, because similar symptoms are present in more prevalent\n   disorders. Symptoms are not specific and include flashing, diarrhea,\n   abdominal pain, right heart disease, bronchoconstriction... and to establish\n   the right diagnosis medical doctor have to think about NET as a possibility.\n   Thus, it is very important to recognize symptoms and signs of the carcinoid\n   syndrome, and distinguish them from other gastrointestinal disorders. Early\n   diagnosis and treatment have significant impact in control of the disease,\n   and overall treatment results.<\/jats:p>","DOI":"10.2298\/aci1303013b","type":"journal-article","created":{"date-parts":[[2014,3,17]],"date-time":"2014-03-17T11:25:53Z","timestamp":1395055553000},"page":"13-16","source":"Crossref","is-referenced-by-count":0,"title":["Carcinoid syndrome in neuroendocrine tumors - not easy to recognize"],"prefix":"10.2298","volume":"60","author":[{"given":"Milos","family":"Bjelovic","sequence":"first","affiliation":[{"name":"Klini\u010dki Centar Srbije, Medicinski fakultet, Centar za hirurgiju jednjaka, Klinika za digestivnu hirurgiju - Prva hirur\u0161ka, Beograd"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1078","container-title":["Acta chirurgica Iugoslavica"],"original-title":[],"language":"en","deposited":{"date-parts":[[2023,5,26]],"date-time":"2023-05-26T12:10:25Z","timestamp":1685103025000},"score":1,"resource":{"primary":{"URL":"https:\/\/doiserbia.nb.rs\/Article.aspx?ID=0354-950X1303013B"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013]]},"references-count":0,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2013]]}},"URL":"https:\/\/doi.org\/10.2298\/aci1303013b","relation":{},"ISSN":["0354-950X","2406-0887"],"issn-type":[{"value":"0354-950X","type":"print"},{"value":"2406-0887","type":"electronic"}],"subject":[],"published":{"date-parts":[[2013]]}}}