سامانه مدیریت نشریات علمی دانشگاه علوم پزشکی مشهد

Yavuz, Sibel, Yıldızdaş, Dinçer, Özgür Horoz, Özden, Özden, Önder, Erdoğan, Kıvılcım Eren, Tuğsan Ballı, Hüseyin, Aikimbaev, Kairgeldy, Önenli Mungan, Halise Neslihan, Tümgor, Gökhan. (1400). A Multifaceted Disease of Problematic Diagnosis in Childhood; Hereditary Hemorrhagic Telangiectasia: A Case Report. , 9(5), 13585-13590. doi: 10.22038/ijp.2021.54438.4306
Sibel Yavuz; Dinçer Yıldızdaş; Özden Özgür Horoz; Önder Özden; Kıvılcım Eren Erdoğan; Hüseyin Tuğsan Ballı; Kairgeldy Aikimbaev; Halise Neslihan Önenli Mungan; Gökhan Tümgor. "A Multifaceted Disease of Problematic Diagnosis in Childhood; Hereditary Hemorrhagic Telangiectasia: A Case Report". , 9, 5, 1400, 13585-13590. doi: 10.22038/ijp.2021.54438.4306
Yavuz, Sibel, Yıldızdaş, Dinçer, Özgür Horoz, Özden, Özden, Önder, Erdoğan, Kıvılcım Eren, Tuğsan Ballı, Hüseyin, Aikimbaev, Kairgeldy, Önenli Mungan, Halise Neslihan, Tümgor, Gökhan. (1400). 'A Multifaceted Disease of Problematic Diagnosis in Childhood; Hereditary Hemorrhagic Telangiectasia: A Case Report', , 9(5), pp. 13585-13590. doi: 10.22038/ijp.2021.54438.4306
Yavuz, Sibel, Yıldızdaş, Dinçer, Özgür Horoz, Özden, Özden, Önder, Erdoğan, Kıvılcım Eren, Tuğsan Ballı, Hüseyin, Aikimbaev, Kairgeldy, Önenli Mungan, Halise Neslihan, Tümgor, Gökhan. A Multifaceted Disease of Problematic Diagnosis in Childhood; Hereditary Hemorrhagic Telangiectasia: A Case Report. , 1400; 9(5): 13585-13590. doi: 10.22038/ijp.2021.54438.4306

A Multifaceted Disease of Problematic Diagnosis in Childhood; Hereditary Hemorrhagic Telangiectasia: A Case Report

Journal of Pediatric Perspectives
مقاله 16، دوره 9، شماره 5 - شماره پیاپی 89، مرداد 2021، صفحه 13585-13590    اصل مقاله (483.89 K)
شناسه دیجیتال (DOI): 10.22038/ijp.2021.54438.4306
نویسندگان
Sibel Yavuz* 1؛ Dinçer Yıldızdaş2؛ Özden Özgür Horoz2؛ Önder Özden3؛ Kıvılcım Eren Erdoğan4؛ Hüseyin Tuğsan Ballı5؛ Kairgeldy Aikimbaev5؛ Halise Neslihan Önenli Mungan6؛ Gökhan Tümgor1
1Cukurova University Medical Faculty, Dept. Of Pediatric Gastroenterology, Adana, Turkey
2Cukurova University Medical Faculty, Dept. Of Pediatric Intensive Care , Adana, Turkey
3Cukurova University Medical Faculty, Dept. Of Pediatric Surgery Adana, Turkey
4Cukurova University Medical Faculty, Dept. Of Pathology, Adana, Turkey
5Cukurova University Medical Faculty, Dept. Of Radiology, Adana, Turkey
6Cukurova University Medical Faculty, Dept. Of Pediatric Metabolısm and Nutrition, Adana, Turkey
چکیده
Hereditary hemorrhagic telangiectasia (HHT) is a vascular dysplasia inherited in an autosomal dominant manner and may involve skin, mucosa, and internal organs. HHT may cause arteriovenous, arterioportal, and portovenous shunts in the liver, resulting in cirrhosis and portal hypertension. An eight-year-old male patient with a diagnosis of myelodysplastic syndrome for two years was admitted with melena. Portal doppler ultrasonography showed a heterogeneous appearance of the liver parenchyma and splenomegaly (spleen size of 14 cm) with no portal hypertension. An extended etiological investigation for chronic liver disease was conducted. Afterliver biopsy, the patient’s general condition deteriorated, with abdominal distension and reduced hematocrit. The Doppler and hepatic angiography results together with a history of recurrent episodes of epistaxis led to the diagnosis of HHT. The patient was referred to the transplant center for liver transplantation due to the irreversible bleeding from the liver. Hepatic telangiectasias may be present in patients without hematologic disorders who have uncontrollable bleeding after liver biopsy.
کلیدواژه‌ها
Children؛ Hereditary hemorrhagic telangiectasia؛ Lıver transplantation
آمار
تعداد مشاهده مقاله: 661
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