{"id":10611,"date":"2018-03-25T21:10:06","date_gmt":"2018-03-25T19:10:06","guid":{"rendered":"http:\/\/medrazgl.si\/en\/?p=10611"},"modified":"2018-03-25T21:10:06","modified_gmt":"2018-03-25T19:10:06","slug":"life-threatening-haemorrhage-due-to-a-spontaneous-aneurysm-rupture-of-the-lienal-artery-in-a-young-patient-with-ehlers-danlos-syndrome-type-iv","status":"publish","type":"post","link":"https:\/\/medrazgl.si\/en\/life-threatening-haemorrhage-due-to-a-spontaneous-aneurysm-rupture-of-the-lienal-artery-in-a-young-patient-with-ehlers-danlos-syndrome-type-iv\/","title":{"rendered":"Life-Threatening Haemorrhage Due to a Spontaneous Aneurysm Rupture of the Lienal Artery in a Young Patient With Ehlers-Danlos Syndrome Type IV"},"content":{"rendered":"<p>Ehlers-Danlos syndrome type IV or vascular type is a rare connective-tissue disorder caused by impaired collagen III synthesis. It occurs due to the mutation in the COL3A1 gene,\u00a0which is inherited or caused sporadically by mutation de novo. Due to collagen III deficit the vascular tissue and tissue of visceral organs is fragile, which leads to numerous life-threatening complications. The most common amongst these are vascular events with dangerous haemorrhages, followed by spontaneous gastrointestinal perforations, ruptures of visceral organs and uterus in pregnancy. The aforementioned complications are in 70% of cases the first manifestation of the disease which is already expressed in young patients. There is no specific therapy, therefore treatment is symptomatic and focused on preventive measures and genetic counselling. Surgical intervention is warranted only in urgent states; non-urgent operations and invasive diagnostic investigations are not advised. Early discovery and monitoring of vascular lesions is important. If lesions imperil patient\u2019s life, we can eliminate them with elective operations before the onset of complications. In the article, we present a case of a 29-year-old patient with known vascular type of Ehlers-Danlos syndrome, whose life was endangered due to an aneurysm rupture of the lienal artery. The origin of the intraabdominal haemorrhage was revealed with CT angiography. The haemorrhage was stopped with a ligature of the lienal artery without splenectomy and the postoperative course passed without complications.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Ehlers-Danlos syndrome type IV or vascular type is a rare connective-tissue disorder caused by impaired collagen III synthesis. It occurs due to the mutation in the COL3A1 gene,\u00a0which is inherited or caused sporadically by mutation de novo. Due to collagen III deficit the vascular tissue and tissue of visceral organs is fragile, which leads to [&hellip;]<\/p>\n","protected":false},"author":41,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":"","_links_to":"","_links_to_target":""},"categories":[811,428,814,427],"tags":[],"class_list":["post-10611","post","type-post","status-publish","format-standard","hentry","category-4-2017-archive","category-clinical-cases","category-kirurgija-en","category-surgery"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Life-Threatening Haemorrhage Due to a Spontaneous Aneurysm Rupture of the Lienal Artery in a Young Patient With Ehlers-Danlos Syndrome Type IV - Dru\u0161tvo Medicinski razgledi<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/medrazgl.si\/zivljenjsko-ogrozujoca-krvavitev-zaradi-spontane-rupture-anevrizme-lienalne-arterije-pri-mladem-bolniku-z-ehlers-danlosovim-sindromom-tipa-iv\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Life-Threatening Haemorrhage Due to a Spontaneous Aneurysm Rupture of the Lienal Artery in a Young Patient With Ehlers-Danlos Syndrome Type IV - Dru\u0161tvo Medicinski razgledi\" \/>\n<meta property=\"og:description\" content=\"Ehlers-Danlos syndrome type IV or vascular type is a rare connective-tissue disorder caused by impaired collagen III synthesis. It occurs due to the mutation in the COL3A1 gene,\u00a0which is inherited or caused sporadically by mutation de novo. Due to collagen III deficit the vascular tissue and tissue of visceral organs is fragile, which leads to [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/medrazgl.si\/zivljenjsko-ogrozujoca-krvavitev-zaradi-spontane-rupture-anevrizme-lienalne-arterije-pri-mladem-bolniku-z-ehlers-danlosovim-sindromom-tipa-iv\/\" \/>\n<meta property=\"og:site_name\" content=\"Dru\u0161tvo Medicinski razgledi\" \/>\n<meta property=\"article:published_time\" content=\"2018-03-25T19:10:06+00:00\" \/>\n<meta name=\"author\" content=\"Tja\u0161a Gortnar\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Tja\u0161a Gortnar\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/medrazgl.si\\\/zivljenjsko-ogrozujoca-krvavitev-zaradi-spontane-rupture-anevrizme-lienalne-arterije-pri-mladem-bolniku-z-ehlers-danlosovim-sindromom-tipa-iv\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/medrazgl.si\\\/zivljenjsko-ogrozujoca-krvavitev-zaradi-spontane-rupture-anevrizme-lienalne-arterije-pri-mladem-bolniku-z-ehlers-danlosovim-sindromom-tipa-iv\\\/\"},\"author\":{\"name\":\"Tja\u0161a Gortnar\",\"@id\":\"https:\\\/\\\/medrazgl.si\\\/#\\\/schema\\\/person\\\/3c51c8c3a0d13f85a32b27a0c2636b0b\"},\"headline\":\"Life-Threatening Haemorrhage Due to a Spontaneous Aneurysm Rupture of the Lienal Artery in a Young Patient With Ehlers-Danlos Syndrome Type IV\",\"datePublished\":\"2018-03-25T19:10:06+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/medrazgl.si\\\/zivljenjsko-ogrozujoca-krvavitev-zaradi-spontane-rupture-anevrizme-lienalne-arterije-pri-mladem-bolniku-z-ehlers-danlosovim-sindromom-tipa-iv\\\/\"},\"wordCount\":248,\"commentCount\":0,\"articleSection\":[\"4\",\"Clinical Cases\",\"Kirurgija\",\"Surgery\"],\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"CommentAction\",\"name\":\"Comment\",\"target\":[\"https:\\\/\\\/medrazgl.si\\\/zivljenjsko-ogrozujoca-krvavitev-zaradi-spontane-rupture-anevrizme-lienalne-arterije-pri-mladem-bolniku-z-ehlers-danlosovim-sindromom-tipa-iv\\\/#respond\"]}]},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/medrazgl.si\\\/zivljenjsko-ogrozujoca-krvavitev-zaradi-spontane-rupture-anevrizme-lienalne-arterije-pri-mladem-bolniku-z-ehlers-danlosovim-sindromom-tipa-iv\\\/\",\"url\":\"https:\\\/\\\/medrazgl.si\\\/zivljenjsko-ogrozujoca-krvavitev-zaradi-spontane-rupture-anevrizme-lienalne-arterije-pri-mladem-bolniku-z-ehlers-danlosovim-sindromom-tipa-iv\\\/\",\"name\":\"Life-Threatening Haemorrhage Due to a Spontaneous Aneurysm Rupture of the Lienal Artery in a Young Patient With Ehlers-Danlos Syndrome Type IV - 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