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A giant choledochal cyst in infancy: a case report
Yurttutan, Nursel,Karakus, Suleyman Cuneyt,Koku, Naim,Demirci, Mustafa,Ucak, Ramazan The Korean Pediatric Society 2016 Clinical and Experimental Pediatrics (CEP) Vol.59 No.5
Choledochal cyst is a dilation that encloses the intrahepatic or both extra- and intrahepatic portions of the biliary ducts. Postnatally, ultrasonography is the initial diagnostic modality of choice, allowing for precise measurements of intra- or extrahepatic duct dilatation and identification of stones and sludge. Symptoms depend on the age at presentation. Common bile duct malformations should be considered as a differential diagnosis of a cystic mass regardless of the cyst's size or patient's age, especially in children presenting with abdominal pain, jaundice, and palpable mass. To the best of our knowledge, we report the largest choledochal cyst in infancy.
A giant choledochal cyst in infancy: a case report
Nursel Yurttutan,Suleyman Cuneyt Karakus,Naim Koku,Mustafa Demirci,Ramazan Ucak 대한소아청소년과학회 2016 Clinical and Experimental Pediatrics (CEP) Vol.59 No.5
Choledochal cyst is a dilation that encloses the intrahepatic or both extra- and intrahepatic portions of the biliary ducts. Postnatally, ultrasonography is the initial diagnostic modality of choice, allowing for precise measurements of intra- or extrahepatic duct dilatation and identification of stones and sludge. Symptoms depend on the age at presentation. Common bile duct malformations should be considered as a differential diagnosis of a cystic mass regardless of the cyst’s size or patient’s age, especially in children presenting with abdominal pain, jaundice, and palpable mass. To the best of our knowledge, we report the largest choledochal cyst in infancy.
Yurttutan, Sadik,Oncel, Mehmet Yekta,Yurttutan, Nursel,Degirmencioglu, Halil,Uras, Nurdan,Dilmen, Ugur The Korean Pediatric Society 2015 Clinical and Experimental Pediatrics (CEP) Vol.58 No.6
Lethargy in newborns usually indicates central nervous system dysfunction, and many conditions such as cerebrovascular events, infections, and metabolic diseases should be considered in the differential diagnosis. Nonketotic hyperglycinemia is an autosomal recessive error of glycine metabolism, characterized by myoclonic jerks, hypotonia, hiccups, apnea, and progressive lethargy that may progress to encephalopathy or even death. Cerebral sinovenous thrombosis is a rare condition with various clinical presentations such as seizures, cerebral edema, lethargy, and encephalopathy. Here, we report the case of a newborn infant who presented with progressive lethargy. An initial diagnosis of cerebral venous sinus thrombosis was followed by confirmation of the presence of nonketotic hyperglycinemia.
Sadık Yurttutan,Mehmet Yekta Oncel,Nursel Yurttutan,Halil Degirmencioglu,Nurdan Uras,Ugur Dilmen 대한소아청소년과학회 2015 Clinical and Experimental Pediatrics (CEP) Vol.58 No.6
Lethargy in newborns usually indicates central nervous system dysfunction, and many conditions such as cerebrovascular events, infections, and metabolic diseases should be considered in the differential diagnosis. Nonketotic hyperglycinemia is an autosomal recessive error of glycine metabolism, characterized by myoclonic jerks, hypotonia, hiccups, apnea, and progressive lethargy that may progress to encephalopathy or even death. Cerebral sinovenous thrombosis is a rare condition with various clinical presentations such as seizures, cerebral edema, lethargy, and encephalopathy. Here, we report the case of a newborn infant who presented with progressive lethargy. An initial diagnosis of cerebral venous sinus thrombosis was followed by confirmation of the presence of nonketotic hyperglycinemia.