11 July 2017: Articles
Development of Graft-Site Candidiasis in 3 Solid Organ Transplant Recipients from the Same Donor
Unusual clinical course, Challenging differential diagnosis, Unusual or unexpected effect of treatment, Diagnostic / therapeutic accidents, Educational Purpose (only if useful for a systematic review or synthesis)
Nasrin El-Bandar ABE 1, Daniela C. Kroy BD 2, Tom Florian Fuller BD 1, Jürgen Kramer BC 3, Lutz Liefeldt BD 4, Klemens Budde BD 4, Conrad Blobel BC 1, Kurt Miller BD 1, Frank Friedersdorff DE 1*DOI: 10.12659/AJCR.904119
Am J Case Rep 2017; 18:777-781
Abstract
BACKGROUND: Graft-site candidiasis rarely develops in solid organ transplant recipients; however, severe life-threatening complications can occur. We report the course of 3 solid organ transplant recipients developing graft-site candidiasis.
CASE REPORT: All grafts, consisting of 2 kidneys and 1 liver, were procured from a single donor. Patient data were collected from our database. Candida albicans was isolated from a swab taken during multiple-organ recovery. Complications associated with candidiasis occurred in all 3 recipients with preservation of the liver transplant. Both renal transplant recipients had vascular complications, eventually resulting in graft nephrectomy and subsequent return to dialysis. The patients recovered completely without residual effects of their prior fungal infection.
CONCLUSIONS: Fungal infections in solid organ transplant recipients are rare. Since the sequelae of these infections are serious and usually pertain to more than 1 recipient at a time, antifungal prophylaxis may be warranted in select donors.
Keywords: Candida albicans, Lung Diseases, Fungal, Transplantation, Homologous
Background
GOOD SCIENTIFIC PRACTICE:
Patient data were recorded with privacy protection and anonymization.
Case Report
DONOR:
Grafts were procured from a 61-year-old female donor following diagnosis of brain death. The donor had an acute flare of chronic pancreatitis with a retro-oesophageal pseudocyst. After several endoscopic interventions, a double-j stent was inserted into the pseudocyst via para-oesophageal puncture, noting a brown secretion. Nevertheless, the patient’s condition deteriorated with development of peritonitis, unclear thrombocytopenia, acute renal failure, and epileptic seizures. However, no schistocytes were found on blood smears. Computed tomography (CT) showed a subdural hematoma and an intracerebral hemorrhage. Despite hemicraniectomy with removal of the hematoma, the patient’s consciousness decreased, eventually resulting in brain death.
Three organs were procured from the donor: 2 kidneys and 1 liver. Multiple-organ procurement and transplantation of the kidneys was conducted at the Charité University Hospital Berlin, and liver transplantation was performed at the RWTH University Hospital Aachen. During multiple-organ procurement, the surgeons noted apparent residues of an inflammatory process. Six days after multiple-organ procurement, physicians were informed about the detection of
KIDNEY TRANSPLANT RECIPIENT 1:
A 33-year-old woman with end-stage renal disease resulting from IgA nephropathy received, after 42 months of hemodialysis, the left kidney of a deceased donor.
During back-table preparation of the kidney, the surgeons noted an adherent renal gland and pararenal tissue, probably corresponding to a 12-mm hypodense mass at the site of the left renal gland on the donor’s CT. The graft was placed in the right iliac fossa with end-to-side anastomosis of the renal vessels to the external iliac vessels. The kidney had good perfusion after 13 h 4 min of cold ischemia time and 50 min of anastomosis time. Ureteroneocystostomy was performed using 2-stitch technique. The patient received triple-drug therapy with tacrolimus, prednisone, and mycophenolate mofetil.
On post-transplant day 6, hemoglobin fell to 4 g/dl. Consequently, an emergency surgery was conducted, identifying insufficiency of the arterial anastomosis, which resulted in acute hemorrhage. Unfortunately, an unsuccessful reconstruction of the arterial anastomosis necessitated an ensuing graft nephrectomy. On the same day, the donor’s swab tested positive for
The patient underwent operative revision 3 times within the following 9 days due to recurrent hemorrhage. The third surgical revision revealed an insufficiency of the vascular suture at the site of the initial arterial anastomosis of the graft. Subsequently, resection of 1.5 cm of the external iliac artery and an ensuing arterial reconstruction were conducted using a saphenous vein interposition graft. In addition to the identification of Candida albicans in microbiological testing, histopathological examination of the resected tissue showed purulent inflammation with fungal colonization (Figure 1).
Seven weeks after transplantation, the patient’s clinical condition improved and she was discharged from hospital. Eventually, following graft nephrectomy, she resumed hemodialysis for treatment of end-stage renal disease and remained under antifungal therapy for 3 months.
KIDNEY TRANSPLANT RECIPIENT 2:
A 58-year-old woman with end-stage renal disease resulting from ureteral strictures caused by schistosomiasis, received a right kidney after undergoing maintenance hemodialysis for 91 months. Renal transplantation was conducted uneventfully, placing the right kidney in the left iliac fossa. Anastomosis of the vessels, ureteroneocystostomy, and immunosuppressive treatment were carried out as in the previous case. The renal graft had good perfusion after 7 h 15 min of cold ischemia time and 46 min of anastomosis time.
Six days after transplantation, the patient had syncope. A CT scan revealed a 12-cm hematoma at the graft site, necessitating an operative revision. During surgery, a hemorrhage from an arterial branch of the graft was identified and the patient developed hemorrhagic shock. Aspiration of gastric contents during the induction of anaesthesia resulted in acute respiratory distress syndrome, contributing, next to liver and graft failure, to multiorgan failure. She was admitted to the Intensive Care Unit, where her condition improved. Swabs from the graft site were positive for
One month after transplantation, the patient reported pain at the graft site. The ensuing CT showed a pseudoaneurysm at the arterial anastomosis, measuring 4.5×2.3 cm (Figure 2). Subsequently, the patient underwent graft nephrectomy with arterial reconstruction using a saphenous vein patch. Subsequently, the patient required hemodialysis owing to end-stage renal disease.
Three months after transplantation, a CT scan once again revealed a pseudoaneurysm at the site of the former arterial anastomosis. Consequently, ligation of the external iliac artery and an ensuing femoro-femoral cross-over bypass with use of a homograft were conducted. There were no further conspicuous or intervention-requiring findings within 4-month follow-up after the last surgery.
LIVER TRANSPLANT RECIPIENT:
Six days after transplantation, the hospital in which liver transplantation was conducted was informed about the adverse events in both kidney transplant recipients. By that time, the 53-year old female liver transplant recipient had not developed any complications. Since we suspected a donor-derived infection, antifungal prophylaxis was immediately initiated using caspofungin.
The liver transplant recipient had alcoholic liver disease and underwent orthotopic liver transplantation due to acute-on-chronic liver failure, with a MELD score of 40. Transplantation was conducted with use of a venovenous bypass. Arterial anastomosis was performed between the donor’s celiac trunk and the recipient’s common hepatic artery at the level of bifurcation. Biliary reconstruction was performed as side-to-side choledochocholedochostomy with placement of a T-tube. The cold ischemia time and the anastomosis time were 8 h and 28 min, respectively, with subsequent good perfusion of the liver. Immunosuppressive therapy consisted of tacrolimus, prednisone, and mycophenolate mofetil.
Despite antifungal prophylaxis, complications could not be prevented. Four weeks after transplantation, the patient developed ascites. Since it could not be managed sufficiently by paracentesis, she underwent operative revision. Surgery revealed a subhepatic abscess with concomitant peritonitis caused by
During the following 5 months, the patient had recurrent cholangitis with identification of various pathogens, including
Figure 3 illustrates the postoperative course of the 3 solid organ transplant recipients presented above.
Discussion
Although lacking of microbiological evidence, we believe the donor had invasive candidiasis. Despite the absence of fungi in the donor`s blood culture, a disseminated infection could not be excluded, since the sensitivity of blood cultures in the detection of
Prevention of
Although antifungal prophylaxis might reduce the incidence and complications of invasive fungal infections, their general use might not be advisable owing to the low incidence rate and the possible emergence of resistance [11, 12]. Moreover, fungal infections at the graft site can occur despite the prophylactic use of antifungal agents, as presented above. However, the use of antifungal agents for prophylaxis of fungal infections may be warranted when graft-site candidiasis occurs in another transplant recipient from the same donor or when the organ perfusate is positive for fungi [3,13].
Complications due to candidiasis most frequently affect the arterial anastomosis and are often associated with a fatal outcome [3,5,9,14–16]. Vascular complications even occur after treatment with antifungals and graft nephrectomy [3,13]. In our patients, we noticed the occurrence of further complications in 1 renal transplant recipient after reconstruction of the arterial anastomosis with a patch. In contrast, the other kidney transplant recipient developed no further complications after resection of 1.5 cm of the vascular tissue at the site of the arterial anastomosis. This suggests that resection of the vascular tissue at the site of the arterial anastomosis is associated with a better outcome when the vascular tissue is affected by fungal infection. Better management of invasive fungal infections might also be achieved by a local intraoperative application of antifungal agents, as in the use of antibiotic bead chains and antibacterial sutures [17–19].
Conclusions
In conclusion, graft-site candidiasis remains a rare complication in solid organ transplant recipients. Nonetheless, due to the possible occurrence of life-threatening and severe complications, a prudent approach is indicated if a fungal infection is suspected. Antifungal prophylaxis should only be conducted in patients at high risk of fungal infections. When vascular complications are observed, graft nephrectomy reduces the risk of life-threatening complications in renal transplant recipients. Direct transmission of infection from the donor, although rarely reported, obviously increases risk of subsequent complications.
References:
1.. Shoham S, Marr KA, Invasive fungal infections in solid organ transplant recipients: Future Microbiol, 2012; 7(5); 639-55, pmid: 22568718
2.. Andes DR, Safdar N, Baddley JW: Transpl Infect Dis, 2016; 18(6); 921-31, pmid: 27643395
3.. Albano L, Bretagne S, Mamzer-Bruneel MF, Evidence that graft-site candidiasis after kidney transplantation is acquired during organ recovery: A multicenter study in France: Clin Infect Dis, 2009; 48(2); 194-202, pmid: 19090753
4.. Gottesdiener KM, Transplanted infections: Donor-to-host transmission with the allograft: Ann Intern Med, 1989; 110(12); 1001-16, pmid: 2658709
5.. Battaglia M, Ditonno P, Fiore T: J Urol, 2000; 163(4); 1236-37, pmid: 10737505
6.. Singh N, Huprikar S, Burdette SD, Donor-derived fungal infections in organ transplant recipients: Guidelines of the American Society of Transplantation, infectious diseases community of practice: Am J Transplant, 2012; 12(9); 2414-28, pmid: 22694672
7.. Guy A, Chinai N, Ashley S: Exp Clin Transplant, 2013; 11(6); 558-61, pmid: 24344947
8.. Kountidou CS, Stier K, Niehues SM, Successful repair of post-transplant mycotic aneurysm of iliac artery with renal graft preservation: A case report: Urology, 2012; 80(5); 1151-53, pmid: 22999448
9.. Addeo P, Saouli AC, Woehl-Jaegle ML: Ann Transplant, 2014; 19; 64-67, pmid: 24487729
10.. Matignon M, Botterel F, Audard V: Am J Transplant, 2008; 8(3); 697-700, pmid: 18294166
11.. Loeffler J, Stevens DA, Antifungal drug resistance: Clin Infect Dis, 2003; 36(Suppl. 1); S31-41, pmid: 12516028
12.. Prigent G, Ait-Ammar N, Levesque E: Antimicrob Agents Chemother, 2017; 61(2); e01229-16, pmid: 27855078 pii
13.. Mai H, Champion L, Ouali N: Transplantation, 2006; 82(9); 1163-67, pmid: 17102767
14.. Levesque E, Suet G, Merle JC: Transpl Infect Dis, 2014; 16(5); 827-29, pmid: 24981194
15.. Llado L, Sole C, Bodro M: Transpl Infect Dis, 2014; 16(3); 465-68, pmid: 24750364
16.. Debska-Slizien A, Chrobak L, Bzoma B: Transpl Infect Dis, 2015; 17(3); 449-55, pmid: 25846286
17.. Klemm KW, Antibiotic bead chains: Clin Orthop Relat Res, 1993(295); 63-76, pmid: 8403672
18.. Storch ML, Rothenburger SJ, Jacinto G: Surg Infect (Larchmt), 2004; 5(3); 281-88, pmid: 15684799
19.. Justinger C, Moussavian MR, Schlueter C, Antibacterial [corrected] coating of abdominal closure sutures and wound infection: Surgery, 2009; 145(3); 330-34, pmid: 19231586
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