Article: A case of drug-induced bullous pemphigoid secondary to immunotherapy treated with upadacitinib: A case report.
SAGE open medical case reports
2023 Volume 11, Page(s) 2050313X231160926
Abstract: Bullous pemphigoid is an acquired autoimmune subepidermal blistering disease that can arise following exposure to systemic medication, referred to as drug-induced bullous pemphigoid. Drug-induced bullous pemphigoid is a rare but potentially serious ... ...
Abstract | Bullous pemphigoid is an acquired autoimmune subepidermal blistering disease that can arise following exposure to systemic medication, referred to as drug-induced bullous pemphigoid. Drug-induced bullous pemphigoid is a rare but potentially serious immune-related adverse event that should be considered in patients with advanced malignancies undergoing immunotherapy, with immune checkpoint inhibitors emerging in particular as a well-documented drug association in drug-induced bullous pemphigoid. We present a 74-year-old female with recurrent metastatic programmed cell death-ligand 1-positive squamous cell carcinoma of the head and neck area who developed drug-induced bullous pemphigoid in the setting of immunotherapy with a novel immunoglobulin-like transcript 4 inhibitor (MK-4830) in combination with pembrolizumab. Treatment with upadacitinib, a Janus-associated kinase-1 inhibitor, was pursued for significantly disabling disease that was recalcitrant to standard therapies and ultimately transition to palliative care. Follow-up at 4 weeks demonstrated good response. This is the first report describing the use of a Janus-associated kinase inhibitor for the treatment of bullous pemphigoid. |
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Language | English |
Publishing date | 2023-03-21 |
Publishing country | England |
Document type | Case Reports |
ZDB-ID | 2736953-5 |
ISSN | 2050-313X |
ISSN | 2050-313X |
DOI | 10.1177/2050313X231160926 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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