| Literature DB >> 6727059 |
F Taketazu, I Sanada, N Ngamatsu, R Mukai, Y Suetomo, N Toyoda, M Takada, K Hida, K Kubota, M Maezawa.
Abstract
A 24-year-old woman was diagnosed as having hereditary elliptocytosis and post-transfusion hepatitis. On admission, a marked delay in indocyanine green (ICG) plasma clearance was noted while bromsulphalein excretion was almost normal. Even when her levels of serum bilirubin and transaminases were decreased to the normal ranges and a liver biopsy revealed no evidence of any liver cirrhosis or active hepatitis, ICG excretion still remained abnormal. These findings were compatible to those of constitutional ICG excretory defect.Entities:
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Year: 1984 PMID: 6727059 DOI: 10.2169/internalmedicine1962.23.139
Source DB: PubMed Journal: Jpn J Med ISSN: 0021-5120