Hemangioma – A pointer to Abernethy syndrome?
نویسندگان
چکیده
منابع مشابه
Abernethy malformation: a case report
BACKGROUND Abernethy malformation is a very rare congenital vascular malformation defined by diversion of portal blood away from liver. It is commonly associated with multiple congenital anomalies. We present a case of Abernethy malformation, without associated congenital anomalies from India. CASE PRESENTATION A 5-year-old female child presented with short history of jaundice. A provisional ...
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Verrucous hemangioma is a rare, localized vascular malformation.The lesions are bluish-red, well demarcated, and compressible. Wereport a case of a 10-year-old girl with coexistent disseminatedverrucous hemangioma and subcutaneous hemangioma overthe nape of neck.
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BACKGROUND Abernethy malformation is a rare congenital anomaly characterised by the partial or complete absence of the portal vein and the subsequent development of an extrahepatic portosystemic shunt. Caroli's disease is a rare congenital condition characterised by non-obstructive saccular intrahepatic bile duct dilation. Caroli's disease combined with congenital hepatic fibrosis and/or renal ...
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Cavernous hemangiomas are the most common benign tumors of the liver. They can reach enormous sizes and cause various complications. Kasabach-Merritt syndrome is a rare but serious complication characterized by consumptive coagulopathy caused by the hemangioma; mortality rate ranges between 10 and 37%. More than 80% of cases occur within the first year of life. Goals of the treatment are to con...
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Pointer information is a prerequisite for most program analyses, and inclusion-based, i.e. Andersen-style, pointer analysis is widely used to compute such information. However, current inclusion-based analyses can have prohibitive costs in time and space, especially for programs with millions of lines of code. We present a suite of offline optimizations that exploit pointer and location equival...
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ژورنال
عنوان ژورنال: Annals of Pediatric Cardiology
سال: 2020
ISSN: 0974-2069
DOI: 10.4103/apc.apc_91_20