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Histopathological and clinical findings in renal transplants with Banff type II and III acute cellular rejection without tubulointerstitial infiltrates
Authors:Verena Bröcker  Muhannad Hirzallah  Wilfried Gwinner  Clemens Luitpold Bockmeyer  Juliane Wittig  Stephanie Zell  Putri Andina Agustian  Anke Schwarz  Tina Ganzenmüller  Eva Zilian  Stephan Immenschuh  Jan Ulrich Becker
Affiliation:1. Institute of Pathology, Hannover Medical School, Carl-Neuberg-Stra?e 1, 30625, Hannover, Germany
6. Department of Histopathology, Addenbrooke’s Hospital, Cambridge, UK
2. Klinikum Region Hannover Krankenhaus Oststadt-Heidehaus, Medizinische Klinik I, Hannover, Germany
3. Clinic for Nephrology and Hypertension, Hannover Medical School, Hannover, Germany
4. Institute of Virology, Hannover Medical School, Hannover, Germany
5. Institute of Transfusion Medicine, Hannover Medical School, Hannover, Germany
Abstract:
According to the Banff guidelines for renal transplants, pure endothelialitis without any tubulointerstitial infiltrates (with the Banff components v?≥?1, i0, t0) has to be called acute cellular rejection (ACR). The pathophysiology of this rare lesion abbreviated as v_only is currently unclear, as well as its clinical, serological, and prognostic implications. Therefore, we conducted this retrospective comparative study. We compared all 23 biopsies with v_only from Hannover Medical School between 2003 and 2010 with 23 matched biopsies with the Banff components v?≥?1, i?≥?1, and t?≥?1 (v_plus) and 23 biopsies with v0, i0, and t0 (v0i0t0). Serological (available in 10, 11, and 14 patients, respectively), histological, and clinical data were compared. Of all biopsies, 0.4 % had findings of v_only. v_only, v_plus, and v0i0t0 only showed minimal differences in the Banff components apart from the cohort-defining components. Endothelialitis in v_only more frequently involved the arcuate arteries than the smaller preglomerular vessels compared to v_plus and vice versa. Combining histopathological data and serological data, v_only more frequently showed criteria for acute humoral rejection than v0i0t0 (albeit not persistent after the Bonferroni–Holm correction in pairwise comparisons), while there was no difference between v_only and v_plus. No difference could be demonstrated regarding clinical presentation at biopsy or outcome. Our results show minimal differences regarding clinical presentation, outcome, and histological features between v_only and v_plus. Patients with v_only should be thoroughly investigated for evidence of acute humoral rejection.
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