AI Article Synopsis

  • - A 72-year-old man with a history of hepatitis C and hepatocellular carcinoma (HCC) experienced fatigue and a skin rash, leading to a diagnosis of dermatomyositis (DM) associated with anti-TIF1-γ antibodies, indicative of HCC recurrence.
  • - Despite treatment with corticosteroids, azathioprine, and intravenous immunoglobulin, he showed only a partial response, leaving him without feasible options for HCC treatment due to poor health, resulting in best supportive care being provided.
  • - The case highlights the link between anti-TIF1-γ antibodies and paraneoplastic DM in HCC, along with the tumor-related aspects of TIF1-γ, which may serve as

Article Abstract

Hepatocellular carcinoma (HCC) is rarely associated with autoimmune paraneoplastic syndromes. We report a case of anti-transcriptional intermediary factor-1 gamma (TIF1-γ)-positive dermatomyositis (DM) as clinical presentation of HCC recurrence in a 72-year-old male patient admitted to our hospital due to fatigue, myalgia, and typical skin rash. His medical history was notable for hepatitis C-related cirrhosis, successful treatment with direct-acting antiviral agents, and previously efficacious treatment of HCC. Laboratory testing showed significant rhabdomyolysis with anti-TIF1-γ antibodies at high titer, and DM was diagnosed. After a careful diagnostic workup, HCC recurrence was diagnosed. After first-line corticosteroid treatment, azathioprine and intravenous immunoglobulin treatments were administered; unfortunately, he mounted only partial response. Owing to the compromised performance status, no HCC treatment was feasible, and, according to international guidelines, he received only best supportive care. Here, we discuss the diagnostic, prognostic, and pathogenic roles of anti-TIF1-γ antibodies associated with paraneoplastic DM and the scant literature data on its occurrence in HCC patients. Considering the TIF1 gene family's established role in oncogenesis, we also review the role of TIF1-γ as a tumor-related neoantigen, leading to the development of clinically overt anti-TIF1-γ antibodies-positive DM.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647099PMC
http://dx.doi.org/10.14218/JCTH.2021.00573DOI Listing

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