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Abstract
Type B insulin resistance (TBIR) is a rare, often fulminant form of insulin resistance caused by
autoantibodies against the insulin receptor. Untreated, its mortality is high. Various
immunosuppressive regimens have shown efficacy, but treatment effects are variable and timedelayed, and drug-induced complications may arise. We report a patient with TBIR arising as a complication of Wiskott–Aldrich syndrome. Stable remission of TBIR was achieved through allogeneic peripheral blood stem cell transplantation (PBSCT) over a follow-up period of more than 1.5 years. We thus demonstrate that PBSCT can be considered a treatment option in TBIR where conventional immunosuppressive therapy is ineffective or contraindicated.
autoantibodies against the insulin receptor. Untreated, its mortality is high. Various
immunosuppressive regimens have shown efficacy, but treatment effects are variable and timedelayed, and drug-induced complications may arise. We report a patient with TBIR arising as a complication of Wiskott–Aldrich syndrome. Stable remission of TBIR was achieved through allogeneic peripheral blood stem cell transplantation (PBSCT) over a follow-up period of more than 1.5 years. We thus demonstrate that PBSCT can be considered a treatment option in TBIR where conventional immunosuppressive therapy is ineffective or contraindicated.
Original language | English |
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Journal | Frontiers in Medicine |
DOIs | |
Publication status | Published - 29 Aug 2023 |
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