Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child
PEDIATRIC GASTROENTEROLOGY HEPATOLOGY & NUTRITION, cilt.21, sa.4, ss.361-364, 2018 (ESCI, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 21 Sayı: 4
- Basım Tarihi: 2018
- Doi Numarası: 10.5223/pghn.2018.21.4.361
- Dergi Adı: PEDIATRIC GASTROENTEROLOGY HEPATOLOGY & NUTRITION
- Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus
- Sayfa Sayıları: ss.361-364
- Karadeniz Teknik Üniversitesi Adresli: Evet
Özet
Accessory hepatic lobe is noted as and considered a rare disease in children. It can manifest with various symptoms and complications depending on the location, volume, type and position of the disease as presented on a child. The patient presented as a 14-month-old girl who was seen with a notable hepatosplenomegaly and portal hypertension. A diagnosis was made after taking an extensive medical history, observation and radiological examinations. The formal diagnosis was a prehepatic portal hypertension associated with accessory hepatic lobe.