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Sequential fulminant hepatitis and toxic epidermal necrolysis induced by tislelizumab: A case report
Zhuo Wang1,2, Chao Li1, Lili Yue2
1Department of Medical Oncology, Liaohua Hospital, Liaoyang, Liaoning 111003, P.R. China.
Immune checkpoint inhibitors (ICIs)-monoclonal antibodies that block inhibitory pathways such as programmed cell death protein 1 (PD-1)/PD-1 ligand to restore T-cell antitumor activity-are increasingly used in advanced non-small cell lung cancer. These agents are associated with severe multisystem immune-related adverse events (irAEs). The present study reported the first case of sequential grade 4 hepatotoxicity and toxic epidermal necrolysis (TEN) induced by the anti-PD-1 antibody tislelizumab. A 70-year-old female patient with advanced lung squamous cell carcinoma developed acute severe mixed liver injury (alanine aminotransferase, 1,741.6 U/l) followed by extensive TEN shortly after initiation of tislelizumab combined with chemotherapy. The toxicities were refractory to conventional hepatoprotective and antihistamine therapies but responded to high-dose corticosteroids combined with intravenous immunoglobulin (IVIG), leading to full recovery. This case highlights that PD-1 inhibitors can induce rare yet life-threatening overlapping irAEs. Clinicians should maintain heightened vigilance for such severe toxicities, particularly in elderly patients receiving combination immunotherapy, and promptly initiate multidisciplinary management including corticosteroids and IVIG.
Immune checkpoint inhibitors (ICIs)-monoclonal antibodies that block inhibitory pathways such as programmed cell death protein 1 (PD-1)/PD-1 ligand to restore T-cell antitumor activity-are increasingly used in advanced non-small cell lung cancer. These agents are associated with severe multisystem immune-related adverse events (irAEs). The present study reported the first case of sequential grade 4 hepatotoxicity and toxic epidermal necrolysis (TEN) induced by the anti-PD-1 antibody tislelizumab. A 70-year-old female patient with advanced lung squamous cell carcinoma developed acute severe mixed liver injury (alanine aminotransferase, 1,741.6 U/l) followed by extensive TEN shortly after initiation of tislelizumab combined with chemotherapy. The toxicities were refractory to conventional hepatoprotective and antihistamine therapies but responded to high-dose corticosteroids combined with intravenous immunoglobulin (IVIG), leading to full recovery. This case highlights that PD-1 inhibitors can induce rare yet life-threatening overlapping irAEs. Clinicians should maintain heightened vigilance for such severe toxicities, particularly in elderly patients receiving combination immunotherapy, and promptly initiate multidisciplinary management including corticosteroids and IVIG.
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