Spider Angioma

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In partnership with Primary Children’s Hospital Skin disorder: Spider angioma A spider angioma (anj-ee-OH-muh) is a cluster of tiny How are spider angiomas treated? red arteries (blood vessels) visible on the skin. It gets Most children’s spider angiomas go away on their its name from the red bump in the center and the own after a while. They rarely bleed and are harmless. surrounding arteries that look like spider legs. Spider If your child’s angioma does not go away, treatments angiomas often appear on the face, arms, hands, may include: fingers, and upper torso. • Electrocoagulation: Removing dilated blood vessels What causes spider angiomas? using a mild electric current No one knows what causes spider angiomas, but your • Pulsed-dye laser therapy: Using a laser with dye to child may be more likely to get a spider angioma if remove angiomas they have: • Liver disease Your child’s doctor will discuss these treatments with you and help you decide what’s best for your child. • Thyroid disease • Hormone changes Notes Intermountain Healthcare complies with applicable federal civil rights laws and does not discriminate on the basis of race, color, national origin, age, disability, or sex. Se proveen servicios de interpretación gratis. Hable con un empleado para solicitarlo. 我們將根據您的需求提供免費的口譯服務。請找尋工作人員協助 © 2018 Intermountain Healthcare, Primary Children’s Hospital. All rights reserved. The content presented here is for your information only. It is not a substitute for professional medical advice, and it should not be used to diagnose or treat a health problem or disease. Please consult your healthcare provider if you have any questions or concerns. More health information is available at intermountainhealthcare.org. Pediatric Education, Practice, and Research 801.662.3500 LTA052 – 06/18 Available in Spanish..

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A Hepatic Outflow Obstruction (Budd-Chiari Syndrome) Case Due
OLGU SUNUMU / CASE REPORT Gülhane Tıp Derg 2014;56: 110-113 © Gülhane Askeri Tıp Akademesi 2014 doi: 10.5455/gulhane.13835 A Hepatic Outflow Obstruction (Budd-Chiari Syndrome) Case Due to Multiple Hypercoagulable Status Yusuf Yazgan (*), Kemal Oncu (*), Mustafa Kaplan (*), Alpaslan Tanoglu (*), İrfan Küçük (*), Halil Onur Ozari (*), Levent Demirturk (*), Murat Velioglu (**) Introduction: SUMMARY Primary Budd-Chiari syndrome (BCS) is a rare disorder We present here a case of a 22-year-old male patient with Budd- caused by thrombosis of the hepatic veins or the terminal Chiari syndrome owing to alliance of multiple hypercoagulable portion of the inferior vena cava. Its estimated incidence ranges conditions. The patient was admitted to our hospital for from 0.2 to 0.8 per million per year (1). In developed countries, assesment of hepatosplenomegaly and ascites. By doppler the hepatic vein thrombosis is the most frequent presentation, ultrasonography, computed tomography and vena cavagraphy, however in developing countries membranous blockade is the Budd-Chiari syndrome was diagnosed. Results of diagnostic tests most common cause of the BCS. BCS is closely associated exhibited decreased activity, decreased antigenic concentration of Antithrombin, low protein C activity, heterozygote Factor with prothrombotic conditions especially with hematologic V Leiden mutation. In clinical progress, acute severe hepatic disorders. For example primary myeloproliferative diseases failure with encephalopathy occured and the patient was (i.e. polycythemia vera) may account for nearly half of the transferred to an another medical center for liver transplantation. all cases (2). Tumors, pregnancy, infections are also other common reasons. Oral contraceptives raise the risk of BCS Key words: Budd-Chiari Syndrome, Antithrombin deficiency, low by nearly two-fold (3).
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1-Dr Zamirian
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M a C S 9 9 9 9 9 4.A NO YES Did Participant Refrain from Caffeine 4.B 1
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