Sequential Passenger Lymphocyte Syndrome and Skin-Predominant Acute Graft-vs-Host Disease After Liver Transplantation

ABSTRACT Passenger lymphocyte syndrome (PLS) and acute graft-vs-host disease (aGVHD) both arise from donor lymphocytes but represent distinct immune-mediated complications rarely documented sequentially in the same recipient. We report a 63-year-old woman who developed severe hemolytic anemia on postoperative day 1 after minor ABO blood group system-mismatched liver transplantation, consistent with PLS, followed 8 weeks later by skin-predominant aGVHD supported by skin biopsy and peripheral blood chimerism. Early diagnosis and treatment with high-dose corticosteroids led to rapid improvement. This case highlights that these complications can occur in sequence and underscores the prognostic importance of organ involvement pattern and early biopsy.

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Publication Details

Journal
ACG Case Reports Journal
Published
2026-09-29
DOI
https://doi.org/10.14309/crj.0000000000002329
Primary Topic
Hematopoietic Stem Cell Transplantation
Type
article
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article

Sequential Passenger Lymphocyte Syndrome and Skin-Predominant Acute Graft-vs-Host Disease After Liver Transplantation

Mary Katherine Rude, Manesh Kumar Gangwani, Yash R. Shah, Matthew G. Deneke et al.
ACG Case Reports Journal
Hematopoietic Stem Cell Transplantation
article

Sequential Passenger Lymphocyte Syndrome and Skin-Predominant Acute Graft-vs-Host Disease After Liver Transplantation

Mary Katherine Rude, Manesh Kumar Gangwani, Yash R. Shah, Matthew G. Deneke, Urveesh Sharma
article en

Abstract

ABSTRACT Passenger lymphocyte syndrome (PLS) and acute graft-vs-host disease (aGVHD) both arise from donor lymphocytes but represent distinct immune-mediated complications rarely documented sequentially in the same recipient. We report a 63-year-old woman who developed severe hemolytic anemia on postoperative day 1 after minor ABO blood group system-mismatched liver transplantation, consistent with PLS, followed 8 weeks later by skin-predominant aGVHD supported by skin biopsy and peripheral blood chimerism. Early diagnosis and treatment with high-dose corticosteroids led to rapid improvement. This case highlights that these complications can occur in sequence and underscores the prognostic importance of organ involvement pattern and early biopsy.

ACG Case Reports JournalVol. 13(10)
University of Arkansas for Medical Sciences (US)
Good health and well-being
Openalex Percentile: Top 12%
Hematopoietic Stem Cell Transplantation
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