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Cholestatic jaundice caused by sequential carbimazole
and propylthiouracil treatment for thyrotoxicosis
AOO Chan, IOL Ng, CM Lam, TWH Shek, CL Lai
Department of Medicine, The University of Hong Kong, Queen Mary
Hospital, Pokfulam Road, Hong Kong
A 36-year-old Chinese man presented to the Queen
Mary Hospital in August 1999 with a 2-week history of jaundice due
to propylthiouracil treatment for thyrotoxicosis. He had previously
received carbimazole but had developed an urticarial skin rash after
2 weeks of treatment. The patient developed liver failure and fulminant
pneumonitis shortly after hospital admission. Despite receiving
treatment with broad-spectrum antibiotics and intravenous immunoglobulin,
he died 11 days after the onset of the respiratory symptoms. Postmortem
examination using electron microscopy showed typical glycogen bodies
within the cytoplasm of the hepatocytes, which corresponded to eosinophilic
cytoplasmic inclusion bodies visible under light microscopy. Immunohistochemical
studies of the inclusion bodies were positive for carcinoembryonic
antigen and albumin, and negative for fibrinogen, complement protein
C3, immunoglobulins G, M, and A, alpha-fetoprotein, and alpha-1-antitrypsin.
This is the first report of a patient who received two sequential
antithyroid drugs and developed predominate cholestasis with unique
histological features. Extreme caution should be taken when a patient
develops allergy to one type of antithyroid drug, because cross
reactivity may develop to the other type.
Hong Kong Med J 2003;9:377-80
Key words: Antithyroid agents; Carbimazole; Cholestasis;
Propylthiouracil
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