A case of drug-induced hypersensitivity syndrome manifesting as toxic epidermal necrolysis-like skin lesions and severe liver injury

Kanzo ◽  
1988 ◽  
Vol 29 (7) ◽  
pp. 949-955 ◽  
Author(s):  
Kazuhiro MATSUEDA ◽  
Yoshiko MATSUOKA ◽  
Motowo MIZUNO ◽  
Toshihiro HIGASHI ◽  
Minoru UKIDA ◽  
...  

1997 ◽  
Vol 136 (4) ◽  
pp. 645-646 ◽  
Author(s):  
P. Redondo ◽  
I. de Felipe ◽  
A. de la Pena ◽  
J.M. Aramendia ◽  
V. Vanaclocha

Hepatology ◽  
2015 ◽  
Vol 63 (3) ◽  
pp. 993-999 ◽  
Author(s):  
Harshad Devarbhavi ◽  
Sujata Raj ◽  
Venu H. Aradya ◽  
Vijaykumar T. Rangegowda ◽  
Girish P. Veeranna ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Anneleen Van Hootegem ◽  
Chris Verslype ◽  
Werner Van Steenbergen

In patients with hepatocellular carcinoma characterized by vascular invasion and/or extrahepatic disease, Sorafenib is considered treatment of choice. Although mild liver test abnormalities were reported in less than 1% of the patients in the two large randomized, controlled phase III trials, four cases of severe acute Sorafenib-induced hepatitis have been described. One of these four cases died from liver failure. In this paper, a patient with HCC with lung metastases developed high fever and a severe hepatitis that rapidly evolved into liver coma and death, two weeks after the initiation of Sorafenib. Biochemical parameters pointed to a hepatocellular type of injury. Clinical and biochemical presentations were compatible with a drug-induced hypersensitivity syndrome such as it has mainly been described for aromatic anticonvulsants, sulphonamides, and allopurinol. We hypothesize that an underlying cytochrome P450 dysfunction with the presence of reactive drug metabolites might lead to this potentially fatal Sorafenib-induced severe liver dysfunction.


2009 ◽  
Vol 71 (6) ◽  
pp. 584-588 ◽  
Author(s):  
Kenji HIROSE ◽  
Yoshihiro MATSUDATE ◽  
Yasutoshi HIDA ◽  
Shin-ichi ANSAI ◽  
Yoshiaki KUBO ◽  
...  

Lupus ◽  
2018 ◽  
Vol 27 (8) ◽  
pp. 1383-1386 ◽  
Author(s):  
B Sunkara ◽  
D Roofeh ◽  
S Silver ◽  
T LeBleu Pearson ◽  
M Ettel ◽  
...  

A 29-year-old woman with a 1.5 year history of photosensitive skin lesions on her hands presented with a malar rash, bullous lesions on her hands, and was diagnosed with subacute lupus erythematosus after serologies revealed a positive antinuclear antibody test (1:2560), and antibodies to Ro/SSA and dsDNA. Hydroxychloroquine (400 mg/day) was prescribed and the patient developed severe drug-induced liver injury. Biopsy of her bullous skin lesions was consistent with porphyria cutanea tarda, as were her serological and urinary exams. She was successfully treated with therapeutic phlebotomy. This case identifies porphyria cutanea tarda as an important differential diagnosis for the rheumatologist to consider when evaluating patients with bullous skin lesions. Hydroxychloroquine in lower doses is an effective treatment for porphyria cutanea tarda; at doses used to treat systemic lupus erythematosus and subacute cutaneous lupus, there is a potentially life-threatening complication of hepatotoxicity.


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