CHẨN ĐOÁN GIẢI PHẪU BỆNH SINH THIẾT THẬN GHÉP THEO HỆ THỐNG PHÂN LOẠI BANFF NĂM 2022

Thùy Linh Nguyễn1, , Phú Ân Tô1, Văn Đồng Tạ1, Quang Anh Đỗ1, Quang Hậu Trần2, Thu Hiền Nguyễn1
1 Bộ môn - Khoa Giải phẫu bệnh lý, Pháp y, Bệnh viện Quân y 103, Học viện Quân y
2 Học viện Quân y

Main Article Content

Abstract

Objectives: The study aims to classify renal allograft pathology based on the updated 2022 Banff Classification. Methods: A cross-sectional descriptive study involving 195 patients who underwent renal allograft biopsy at Military Hospital 103 from January 2021 to December 2024. Results: Male patients accounted for 77.43%, with an average age of 38,94 ± 10,66 years. Living donors contributed to 98.98% of the cases. The most common cause of renal allograft dysfunction was rejection (49.23%), including antibody-mediated rejection (AMR) and T-cell-mediated rejection (TCMR). The earliest histological lesions were microvascular inflammation/injury (MVI) and acute AMR, occurring at an average of 0.13±0,07 and 0.58±1.19 months, respectively, while focal segmental glomerulosclerosis (FSGS) appeared the latest, at an average of 92±86.1 months. Patients of category 1 had mild increases in serum creatinine, while patients of category 6 had the highest creatinine levels.


Conclusions: The timing of the development of various etiologies and the use of prebiopsy serum creatinine levels can help in the prediction of etiology of renal dysfunction. However, due to the considerable diversity of allograft pathologies and ongoing updates in new classification, applying the 2022 Banff one is essential.

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References

1. Katsuma A, Yamakawa T, Nakada Y, Yamamoto I, Yokoo T. Histopathological findings in transplanted kidneys. Renal Replacement Therapy. 2017; 3(1):6.
2. Naesens M, Roufosse C, Haas M, et al. The Banff 2022 Kidney Meeting Report: Reappraisal of microvascular inflammation and the role of biopsy-based transcript diagnostics. American Journal of Transplantation. 2024; 24(3):338-349.
3. Bashir S, Hussain M, Ali Khan A, et al. Renal transplant pathology: Demographic features and histopathological analysis of the causes of graft dysfunction. Int J Nephrol. 2020:7289701.
4. Maraghi E, Rahimi Foroushani A, Younespour S, et al. Longitudinal assessment of serum creatinine levels on graft survival after renal transplantation: Joint modeling approach. Nephrourol Mon. Jul 2016; 8(4):e37666.
5. Filippone EJ, McCue PA, Farber JL. Transplant glomerulopathy. Modern Pathology. 2018; 31(2):235-252.
6. Torres IB, Salcedo M, Moreso F, et al. Comparing transplant glomerulopathy in the absence of C4d deposition and donor-specific antibodies to chronic antibody-mediated rejection. Clin Transplant. Oct 2014; 28(10):1148-1154.
7. Ponticelli C, Moroni G, Glassock RJ. De novo glomerular diseases after renal transplantation. Clin J Am Soc Nephrol. Aug 7, 2014; 9(8):1479-1487.