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Ipilimumab induced digital vasculitis

dc.contributor.authorPadda, Amrita
dc.contributor.authorSchiopu, Elena
dc.contributor.authorSovich, Justin
dc.contributor.authorMa, Vincent
dc.contributor.authorAlva, Ajjai
dc.contributor.authorFecher, Leslie
dc.date.accessioned2018-02-18T04:20:20Z
dc.date.available2018-02-18T04:20:20Z
dc.date.issued2018-02-12
dc.identifier.citationJournal for ImmunoTherapy of Cancer. 2018 Feb 12;6(1):12
dc.identifier.urihttp://dx.doi.org/10.1186/s40425-018-0321-2
dc.identifier.urihttps://hdl.handle.net/2027.42/142381
dc.description.abstractAbstract Background Immune check point inhibitors (ICIs) have emerged as a new therapeutic paradigm for a variety of malignancies including metastatic melanoma. As the use of ICIs expand, immune-mediated adverse events are becoming a common occurrence. Case presentation We describe the first reported patient with small vessel vasculitis, manifested by digital ischemia, following treatment with high dose Ipilimumab for resected stage IIIB/C melanoma. This patient received high dose steroids, five-day intravenous (IV) Epoprostenol protocol, botulinum toxin injections, and Rituximab 375 mg/m2 weekly for four cycles. With this treatment regimen, the digital ischemia did not progress proximally, but she did require multiple distal digit amputations about six months after the onset of her symptoms. Conclusions Prompt identification and management of immune related adverse events (IRAEs) are critical to optimal patient management. This patient’s vasculitis did not reverse, but was likely halted and stabilized with multiple immunosuppressive medications.
dc.titleIpilimumab induced digital vasculitis
dc.typeArticleen_US
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/142381/1/40425_2018_Article_321.pdf
dc.language.rfc3066en
dc.rights.holderThe Author(s).
dc.date.updated2018-02-18T04:20:21Z
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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