{"version":"1.0","provider_name":"Geenidiagnostiikka","provider_url":"https:\/\/sites.uef.fi\/genediagnostics","title":"Feokromosytooma - Geenidiagnostiikka","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"2niQdQZdHd\"><a href=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/feokromosytooma\/\">Feokromosytooma<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/sites.uef.fi\/genediagnostics\/monogeeniset-sairaudet\/feokromosytooma\/embed\/#?secret=2niQdQZdHd\" width=\"600\" height=\"338\" title=\"&#8221;Feokromosytooma&#8221; &#8212; Geenidiagnostiikka\" data-secret=\"2niQdQZdHd\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/sites.uef.fi\/genediagnostics\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","thumbnail_url":"https:\/\/sites.uef.fi\/genediagnostics\/wp-content\/uploads\/sites\/100\/2020\/06\/T321_cmyk_15189-3-e1593515084545.jpg","thumbnail_width":169,"thumbnail_height":107,"description":"Feokromosytooma on lis\u00e4munuaisen ytimen yleens\u00e4 hyv\u00e4nlaatuinen kasvain (n. 10 % kasvaimista pahanlaatuisia). Se voi joskus sijaita lis\u00e4munuaisen ulkopuolellakin, jolloin sit\u00e4 kutsutaan paraganglioomiksi. Ne ovat useammin perinn\u00f6llisi\u00e4. Kasvaimessa syntyy katekoliamiineja, adrenaliinia ja noradrenaliinia, jotka aiheuttavat feokromosytoomataudille tyypilliset oireet (kohtauksittainen p\u00e4\u00e4ns\u00e4rky, hikoilu ja nopealy\u00f6ntisyys sek\u00e4 kohonnut verenpaine). Feokromosyytooma tai paragangliooma voi olla joko sproradinen tai familiaalinen (ORPHA: [&hellip;]"}