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. 2022 Dec 30;15(1):115. doi: 10.3390/v15010115

Table 4.

Profiles of the 2 recipients with biopsy-proven CMV colitis after living donor liver transplantation.

Category Recipient No. 1 Recipient No. 2
Age (years) 67 59
Gender Male Female
Etiology of underlying liver disease Non-B, non-C liver cirrhosis Angiosarcoma, ruptured
Clinical symptoms Abdominal pain, diarrhea Abdominal pain
Lesion site Transverse colon
Descending colon
Ascending colon
Transverse colon
Sigmoid colon
Colonoscopy findings Segmental ulcer with intra-luminal narrowing Patchy ulcers
Serum laboratory test
Recipient
Anti-CMV IgM
 Pre-transplant, Index Negative (0.08) Negative (0.19)
 Post-transplant (at time of disease), Index Negative (0.06) Negative (0.34)
Anti-CMV IgG
 Pre-transplant, AU/mL Positive (2115.3) Positive (73.6)
 Post-transplant (at time of disease), AU/mL Positive (1199.3) Positive (2280.9)
CMV-DNA PCR (at time of disease) IU/mL Not detectable Positive (123)
WBC (at time of disease) 1000/uL 16.2 6.2
CRP (at time of disease) mg/L 89.72 9.7
N/L ratio 2.99 0.93
Donor
Anti-CMV IgM (Index) Negative (0.08) Negative (0.06)
Anti-CMV IgG (AU/mL) Positive (615.3) Negative (1.8)
CMV-DNA PCR (IU/mL) Not available Not available
Pathology
 Inclusion bodies Present Present
 CMV IHC staining Positive Positive
Anti-viral medication
 Ganciclovir 14 days 12 days
 Valganciclovir 90 days 160 days
Anti-viral medication duration (days) 104 days 172 days
Time to disease 10 years after LDLT 2 months after LDLT
Immunosuppressants use at time of CMV colitis Mycophenolate mofetil 250mg Q12H PO, Tacrolimus 1mg QD PO Mycophenolate mofetil 500 mg Q12H PO
Prednisolone 5mg TID PO
Tacrolimus 2mg QD PO
Post-LDLT outcomes
 Allograft dysfunction No No
 Biliary tract stricture No Present
 Acute cellular rejection Yes No