TY - JOUR
T1 - A case of adult-onset type II citrullinemia induced by hospital diet
AU - Ueda, Akira
AU - Okada, Kazuhiko
AU - Takahara, Terumi
AU - Iwasa, Keiichi
AU - Shinagawa, Kazuko
AU - Entani, Akio
AU - Inatsuchi, Syuji
AU - Ando, Takayuki
AU - Fujinami, Haruka
AU - Tajiri, Kazuto
AU - Tokimitsu, Yoshiharu
AU - Ogawa, Kohei
AU - Miyazono, Takayoshi
AU - Miyazaki, Takako
AU - Murakami, Jun
AU - Hosokawa, Ayumu
AU - Yasumura, Satoshi
AU - Minemura, Masami
AU - Kudo, Takahiko
AU - Sugiyama, Toshiro
PY - 2011/2
Y1 - 2011/2
N2 - A 47-year-old Japanese man was first admitted to our hospital for 8 days because of an asthma attack. After discharge he changed his diet. On the 12th day after his discharge, he was re-admitted to our hospital because he exhibited transient loss of consciousness with flapping tremor. His plasma ammonia level was extremely high (245 μg/dL; normal, <90 μg/dL), suggesting hepatic encephalopathy. He underwent intravenous administration of branched-chain amino acids (Aminoleban®) and oral administration of lactulose and kanamycin sulfate; however, the hyperammonemia did not improve. Analysis of the amino acids and citrin gene led to the diagnosis of adult-onset type II citrullinemia (CTLN2). Following this diagnosis, the carbohydrate content of his diet was mildly restricted. As a result, his plasma ammonia level markedly improved (ammonia, 40-60 μg/dL) and he became symptom-free without any medication. CTLN2 is a metabolic disorder characterized by increased plasma concentrations of citrulline and ammonia, which occurs by the failure of compensatory mechanisms associated with diet. Here, we report a case of a patient for whom a change in eating habits during his hospitalization disturbed his compensatory mechanism resulting in clinical CTLN2, which was reversed with an appropriate diet.
AB - A 47-year-old Japanese man was first admitted to our hospital for 8 days because of an asthma attack. After discharge he changed his diet. On the 12th day after his discharge, he was re-admitted to our hospital because he exhibited transient loss of consciousness with flapping tremor. His plasma ammonia level was extremely high (245 μg/dL; normal, <90 μg/dL), suggesting hepatic encephalopathy. He underwent intravenous administration of branched-chain amino acids (Aminoleban®) and oral administration of lactulose and kanamycin sulfate; however, the hyperammonemia did not improve. Analysis of the amino acids and citrin gene led to the diagnosis of adult-onset type II citrullinemia (CTLN2). Following this diagnosis, the carbohydrate content of his diet was mildly restricted. As a result, his plasma ammonia level markedly improved (ammonia, 40-60 μg/dL) and he became symptom-free without any medication. CTLN2 is a metabolic disorder characterized by increased plasma concentrations of citrulline and ammonia, which occurs by the failure of compensatory mechanisms associated with diet. Here, we report a case of a patient for whom a change in eating habits during his hospitalization disturbed his compensatory mechanism resulting in clinical CTLN2, which was reversed with an appropriate diet.
KW - CTLN2
KW - Citrin
KW - Citrullinemia
KW - Hepatic encephalopathy
KW - Hyperammonemia
KW - SLC25A13
UR - http://www.scopus.com/inward/record.url?scp=79952187328&partnerID=8YFLogxK
U2 - 10.1007/s12328-010-0188-3
DO - 10.1007/s12328-010-0188-3
M3 - 学術論文
C2 - 26190618
AN - SCOPUS:79952187328
SN - 1865-7257
VL - 4
SP - 28
EP - 33
JO - Clinical Journal of Gastroenterology
JF - Clinical Journal of Gastroenterology
IS - 1
ER -