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Not All Blue is Bad – Donor Derived Rhabdomyolysis in a Cadaveric Kidney Transplant
Corresponding author: Deepak Kumar Selvanathan, Department of Nephrology, Dr. Kamakshi Memorial Hospital, Pallikaranai, Chennai, Tamil Nadu, India. E-mail: dee170388@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Selvanathan DK, Venkatesan G, Velankanni S, Kalimuthu R. Not All Blue is Bad - Donor Derived Rhabdomyolysis in a Cadaveric Kidney Transplant. Indian J Nephrol. doi: 10.25259/IJN_198_2025
Dear Editor,
A 49-year-old female underwent deceased donor kidney transplantation after being on dialysis for 6 years. The donor was a 29-year-old male who had suffered a road traffic accident. The total warm and cold ischemia times were 2 and 13 hours, respectively. The graft showed bluish discoloration during extraction (donor creatinine: 1.9 mg/dL) [Figure 1a]. Post-operatively, she developed anuria and required seven hemodialysis sessions. Allograft biopsy, done on post-operative day (POD) 5, revealed severe acute tubular injury with myoglobin casts [Figure 1b]. The donor’s creatine kinase was not measured, and the recipient’s was normal. A repeat biopsy at day 10 revealed resolving acute tubular injury with disappearance of casts. The urine output improved on POD 17, and she was discharged with a serum creatinine of 2.3 mg/dL). She attained normal graft function (creatinine: 1.1 mg/dL) on POD 25. The creatinine is 0.9 mg/dL 13 months post-transplant.

- (a) Bluish discoloration at the time of retrieval. (b) Post-operative day 5 biopsy showing myoglobin cast deposition within the tubules. Image courtesy: RENOPATH.
Kidney transplantation from donors with acute kidney injury (AKI) could be considered in preventing organ discards. The causes of discolored kidneys include severe cortical necrosis, massive microthrombi, renal hemosiderosis, melanin/lipofuscin pigment deposits, and rhabdomyolysis.1 Rhabdomyolysis-related donor AKI may raise concerns regarding renal hypofunction and primary nonfunction. Postulated mechanisms include intratubular myoglobulin casts, afferent arteriolar vasoconstriction, and direct oxidative damage due to heme-proteins.2 Joshi et al.3 and Takada et al.4 reported normal graft function in five patients, after 79 and 24 months of cadaveric transplant, respectively. Optimal donor management with urinary alkalinization and adequate output may achieve excellent long-term graft outcomes, even in anuric or discolored kidneys.
Conflicts of interest
There are no conflicts of interest.
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