When donor T cells attack: The curious case of liver transplant-associated acute graft-versus-host-disease

Graft versus host disease is a rare but deadly complication of solid organ transplant. Clinical features of graft-versus-host-disease are non-specific, which may lead to delayed diagnosis as more common conditions including infections or drug reactions are considered. We describe a 54-year-old male...

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Veröffentlicht in:Science progress (1916) 2022-07, Vol.105 (3), p.368504221117070-368504221117070
Hauptverfasser: Deschner, Max, Bastin, Donald J., Solh, Ziad, Bosma, Karen, Haddara, Wael, Yang, Ping, Broadbent, Robert, Haig, Aaron, Keow, Jonathan, Brahmania, Mayur, Xenocostas, Anargyros, Deotare, Uday
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Sprache:eng
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Zusammenfassung:Graft versus host disease is a rare but deadly complication of solid organ transplant. Clinical features of graft-versus-host-disease are non-specific, which may lead to delayed diagnosis as more common conditions including infections or drug reactions are considered. We describe a 54-year-old male patient who underwent liver transplantation for alcohol use disorder-related cirrhosis and developed acute graft-versus-host disease. Initial clinical presentation included dermatitis, bone marrow failure and enteritis. Results of skin biopsy and cytogenetic studies were consistent with liver transplant-associated acute graft-versus-host disease. The importance of this case is to highlight to transplant physicians and surgeons the challenges of diagnosing graft-versus-host-disease. In our case, pre-existing partnerships among the liver and hematopoietic stem cell transplant teams, transfusion medicine specialists, critical care specialists and facilitated timely communication relevant to confirming graft-versus-host disease. We propose an algorithm to assist in the workup of suspected graft-versus-host disease. Because this condition is characterized by high mortality, a high index of suspicion is imperative for prompt diagnosis and optimal management of the donor-recipient immune interaction when patients present with classic clinical features.
ISSN:0036-8504
2047-7163
DOI:10.1177/00368504221117070