- Case report
- Open Access
A case report of recurrent membranoproliferative glomerulonephritis after kidney transplantation due to ventriculoatrial shunt infection
BMC Nephrology volume 20, Article number: 296 (2019)
Transplant failure requires the consideration of numerous potential causes including rejection, acute tubular necrosis, infection, and recurrence of the original kidney disease. Kidney biopsy is generally required to approach these differential diagnoses. However, the histopathological findings on their own do not always lead to a definite diagnosis. Consequently, it is crucial to integrate them with clinical findings and patient history when discussing histopathological patterns of injury. The histopathologic finding of a membranoproliferative glomerulonephritis (MPGN) is one of the most challenging constellations since it does not refer to a specific disease entity but rather reflects a pattern of injury that is the result of many different causes. Whilst MPGN is occasionally classified as immune complex mediated, careful evaluation usually reveals an underlying disorder such as chronic infection, plasma cell dyscrasia, complement disorders, and autoimmune disease.
We describe the case of a 43-year-old woman who was referred to us because of a slowly rising serum creatinine 4 years after kidney transplantation. As in the native kidney, the biopsy revealed an MPGN pattern of injury. The cause of this finding had not been established prior to transplantation leading to a classification as idiopathic MPGN in the past. Further workup at the time of presentation and allograft failure revealed chronic infection of a ventriculoatrial shunt as the most probable cause.
This case underlines the fact that MPGN is not a disease but a histopathological description. Consequently, the causative disorder needs to be identified to avoid kidney failure and recurrence after transplantation.
Allograft failure can be caused by numerous differential diagnoses and usually requires kidney biopsy to confirm the actual pathology. Since one of these is recurrence of the disease leading to failure of the native kidneys, a lack of knowledge regarding this point adds to the challenge for nephrologists and nephropathologists. Even in patients in whom the native kidneys were biopsied, the histopathological diagnosis does not automatically lead to a clinical diagnosis. Most commonly, this is the case if the histopathological pattern of injury can be caused by numerous different clinical entities and if the underlying disease is generally rare. MPGN is such a finding with a number of different disorders – most of which are very rare – that can cause the same histopathological picture (Fig. 1) . With chronic infections being one of the possible causes, shunt-nephritis may not be the first thought of many clinicians due to its low incidence. This holds true especially in the setting of transplant failure. Shunt-nephritis refers to a form of glomerulonephritis that is often characterized by an MPGN pattern on the histological level associated with polyclonal immune complexesin subacute and chronic courses while acute courses may present as endocapillary or extracapillary diffuse-proliferative, mesangiocapillary, and mesangial lesions [2,3,4,5].
In the case presented here, MPGN is the consequence of immune-complex deposition induced by chronic infection. Chronic infections of a ventriculoatrial or –peritoneal shunts are most commonly caused by colonization with slowly-growing bacteria of the skin flora, e.g. staphylococci [3, 4]. Many cases of these infections are characterized by a subacute to chronic clinical course (such as recurrent fever, hepatosplenomegaly, and cerebral symptoms). However, very slow chronic and oligosymptomatic courses have also been described [5, 6]. Apart from the unspecific clinical picture, problems in cultivating slowly growing bacteria from blood and liquor cultures make both the diagnosis and a targeted anti-infective therapy difficult. Consequently, these cases are prone to be misinterpreted and diagnosed late when immunological complications such as shunt nephritis have already manifested. However, if recurrent MPGN threatens graft survival, identification of this rare cause is crucial since this problem can be addressed specifically by removing the shunt material and treating with antibiotics according to the resistogram. Finding a way to remove all artificial materials and solving the problem causing hydrocephalus in such a patient without reimplantation of a new shunt are of utmost importance. Here, we present the exemplary case of a young woman illustrating both the differential diagnosis of diseases underlying recurrent MPGN in kidney transplants including the algorithm to identifying shunt nephritis as the causative disorder and the interdisciplinary approach to solving the problem.
Diagnosis of hydrocephalus|
Placement of ventriculoperitoneal shunt
|1992||Placement of ventriculoatrial shunt|
|2004||Diagnosis of membranoproliferative glomerulonephritis|
|2004–2008||Immunosuppressive therapy with cyclosporine and steroids|
|2008||Placement of a AV fistula as dialysis access|
|Feb 2012||Kidney transplantation (cadaveric donor)|
|Mar 2012||Allograft biopsy: No sign of rejection|
|Jun 2012||Allograft biopsy: Borderline T cell-mediated rejection, steroid pulse|
Allograft biopsy: Recurrence of MPGN|
Surgical removal of remaining shunt fragments|
Transcutaneous-endovascular retrieval of VA-shunt fragments
|Oct 2018||Improved allograft function, complete resolution of hematuria and proteinuria|
A 43-year-old Caucasian woman, who had undergone cadaveric kidney transplantation 4 years earlier, was referred to us due to a creeping rise in serum creatinine. Her medication included cyclosporine, mycophenolate-mofetil, prednisone, omeprazole, and oral sodium bicarbonate. She had been on hemodialysis for 3 years before receiving the allograft. To determine the diagnosis leading to end-stage renal disease, a native kidney biopsy had been performed 12 years ago showing MPGN in histopathology. According to her file, a further diagnostic workup back then had not revealed any signs of an underlying condition leading to the classification as idiopathic MPGN. However, due to the long time passed, no data was available regarding the details of the exams that had been performed. Upon presentation, the patient reported malaise, elevated body temperature and shivering when combing her hair or working over-head. She had been experiencing occasional milder episodes of unclear infection during the last decades. Aside from an elevated arterial pressure of 165/85 mmHg, the physical examination was unremarkable. We conducted a complete laboratory blood analysis, which showed a serum creatinine of 183 μmol/L (eGFR CKD-EPI 24 ml/min; best creatinine after transplantation: 92.3 μmol/L, eGFR 56.1 ml/min), a mildly elevated c-reactive protein of 275 nmol/L (28.9 mg/L), a significantly increased procalcitonin (11.1 μg/L), low C3 complement (0.78 g/L), and cyclosporine levels within the target range. The initial urine analysis revealed microhematuria with mild albuminuria of 49 mg/g creatinine. Repeated blood and urine microbial cultures remained sterile. Ultrasound examination of the transplant kidney revealed a normal size without parenchymal or vascular abnormalities. Kidney biopsy showed an active endocapillary proliferative glomerulonephritis - consistent with an early stage of recurrent membranoproliferative glomerulonephritis type I (Fig. 2) with electron dense subendothelial deposits lacking significant glomerular basement membrane splitting. Deposits were positive for IgM, C1q and C4d, with IgA, IgG and C3c virtually negative, excluding a C3-glomerulopathy. Serological studies for human immunodeficiency virus, hepatitis virus, Epstein-Barr virus, cytomegalovirus, parvovirus B19 showed no signs of active disease. Monoclonal gammopathy was excluded by serum and urine immuneelectrophoresis and a serum free light-chain assay. Transesophageal echocardiography demonstrated absence of endocarditic vegetations. Other infectious foci were excluded by sonography and clinical examination. DsDNA-antibodies, anti-neutrophil antibodies, and donor-specific antibodies were not detected. We found anti-nuclear antibodies (subtype SS-A / Ro-60) with a titer of 1:320. Apart from the transplant dysfunction there were no clinical signs of specific autoimmune diseases. The patient did not report recent travels to foreign countries. A ventriculoperitoneal shunt (VP) had been placed at the age of 14 due to congenital aqueductal stenosis and hydrocephalus. At the age of 21 the VP shunt had been switched to a ventriculoatrial shunt (VA) due to recurrent abdominal pain. It had not been possible to recover remnants of the VP-shunt, which had remained in situ.
Shivering on working over-head, recurrent laboratory signs of inflammation, and excluding other causes of MPGN were the clinical cues that led us to suspect a chronically infected VA-shunt as trigger of transplant failure.
To assess the feasibility of shunt removal, we conducted an MRI of the cerebrospinal fluid circulation and interspaces. Imaging revealed a triventricular hydrocephalus with aqueductal stenosis but patent interventricular foramina. Thus, the patient was subjected to endoscopic ventriculocisternostomy and placement of an external liquor drainage, which was removed as soon as the ventriculocisternostomy had proven to drain liquor efficiently. VP- and VA-shunt material was removed surgically. Due to extensive calcification of the VA-shunt-fragment in the superior VC, a 5 cm fragment could not be mobilized manually and had to be removed interventionally via femoral vein access, thus obviating open cardiothoracic surgery. The calcifications remained in place. Despite negative blood and cerebrospinal fluid (CSF)-cultures, microbial analysis detected Staphylococcus hominis and epidermidis on the VP-shunt and Staphylococcus epidermidis on the atrial catheter fragment. All recovered intracranial material remained culture-negative. In accordance with the resistogram, flucloxacilline (3 g IV QID) was administered for 14 days intravenously; antibiotic therapy was continued for another ten days using amoxicillin/clavulanic acid (500/125 mg PO TID). Kidney function began to improve immediately after shunt removal, serum creatinine reached 119.8 μmol/L (eGFR 40 ml/min) 10 weeks after shunt extraction. Hematuria improved in parallel. There were no new episodes of fever and shivering while inflammation parameters returned to normal. The patient did not show any neurological symptoms and was discharged after a course of 39 days. Ever since completion of antibiotic therapy our patient has been free of any renal or systemic symptoms of infection at the last follow-up approximately 1.5 years after shunt removal. Allograft function has improved since discharge (last eGFR 46 ml/min). With complete resolution of hematuria and microalbuminuria, the patient shows no remaining signs of glomerular disease.
Discussion and conclusion
This case clearly illustrates that MPGN must not be considered a disease entity but a histopathological pattern. This pattern can be caused by numerous underlying diseases, many of which are rare by themselves . In transplant kidneys even antibody-mediated rejection and hepatitis C-virus infection can show this pattern [8, 9]. In our patient, disease recurrence was likely. Yet, the nature of the underlying disease had not been elucidated prior to transplantation and needed to be established to direct therapy. Etiology of MPGN can be grouped into 1. polyclonal immune-complex mediated, 2. monoclonal immunoglobuline deposition related, 3. C3-dominant cases and 4. as a result of primary endothelial injury. Workup of patients with an MPGN (or an endocapillary proliferative glomerulonephritis) pattern after exclusion of C3-glomerulopathy requires exclusion of chronic infections, autoimmune disease, adverse drug effects, and hematological neoplasia (Fig. 1). In the course of this workup, it is crucial that all rare causes are excluded. The term idiopathic or primary MPGN mainly reflects incomplete workup missing the underlying etiology. Shunt nephritis as one of these rare infectious causes falls into the category of MPGN related to polyclonal immune-complexes and arises through immune complex chronic antigenemia and polyclonal immune complex deposition in the glomerular tuft, classically presenting with IgM-dominant immune complex deposits like in our case [7, 10]. Colonization with Staphylococcus epidermidis is believed to be the most frequent cause of shunt nephritis although multiple other pathogens have been identified [6, 11,12,13,14]. Similar processes can take place in case of bacterial endocarditis. Shunt nephritis can manifest as diffuse endocapillary proliferative glomerulonephritis similar to poststreptococcal GN, as mesangioproliferative GN, or as MPGN . The severity of GN predominantly depends on the duration of antigenemia and chronic infection. Most cases have a subacute course with neurological symptoms and rapid decline of kidney function so that early shunt removal is critical. If complete shunt removal is possible, renal prognosis is favorable .
The case presented clearly shows the importance of being aware of shunt nephritis as a differential diagnosis of diseases underlying MPGN or endocapillary proliferative GN. In hindsight, it is highly likely that the MPGN in the patient’s native kidneys was in fact shunt nephritis. However, due to an equivocal clinical picture and a lack of alternative therapeutic options at that time, the shunt had remained in place. Differently from most cases reported so far, our patient presented with a rather chronic course of the disease - as indicated by persistently negative blood and CSF-cultures and lack of neurological symptoms – which may be the consequence of slowly growing bacteria with low pathogenicity.
The remaining calcifications in the superior VC may still harbor pathogens causing persistent antigenemia potentially leading to immune complex formation and deposition. However, in contrast to artificial shunt material, which is predisposed to staphylococcal biofilm formation, calcifications undergo constant turnover so that innate host immune mechanisms may clear remaining pathogens. The optimal duration of antibiotic therapy after shunt removal remains to be determined.
Availability of data and materials
The data set used in this study has been reported in the case presentation. Additional clinical data and laboratory values are available upon request from the corresponding author.
Anti-neutrophil cytoplasmic antibody
Double stranded desoxyribonucleic acid
Magnetic resonance imaging
Sethi S, Fervenza FC. Membranoproliferative glomerulonephritis — a new look at an old entity. N Engl J Med. 2012;366(12):1119–31.
Ohara S, Kawasaki Y, Takano K, Isome M, Nozawa R, Suzuki H, et al. Glomerulonephritis associated with chronic infection from long-term central venous catheterization. Pediatr Nephrol Berl Ger. 2006;21(3):427–9.
Arze RS, Rashid H, Morley R, Ward MK, Kerr DN. Shunt nephritis: report of two cases and review of the literature. Clin Nephrol. 1983 Jan;19(1):48–53.
Haffner D, Schindera F, Aschoff A, Matthias S, Waldherr R, Schärer K. The clinical spectrum of shunt nephritis. Nephrol Dial Transplant Off Publ Eur Dial Transpl Assoc - Eur Ren Assoc. 1997;12(6):1143–8.
Kiryluk K, Preddie D, D’Agati VD, Isom R. A young man with Propionibacterium acnes-induced shunt nephritis. Kidney Int. 2008;73(12):1434–40.
Groeneveld AB, Nommensen FE, Mullink H, Ooms EC, Bode WA. Shunt nephritis associated with Propionibacterium acnes with demonstration of the antigen in the glomeruli. Nephron. 1982;32(4):365–9.
Cook HT, Pickering MC. Histopathology of MPGN and C3 glomerulopathies. Nat Rev Nephrol. 2015;11(1):14–22.
Kamar N, Izopet J, Alric L, Guilbeaud-Frugier C, Rostaing L. Hepatitis C virus-related kidney disease: an overview. Clin Nephrol. 2008;69(3):149–60.
Grau V, Zeuschner P, Immenschuh S, Bockmeyer CL, Zell S, Wittig J, et al. Immune complex-type deposits in the Fischer-344 to Lewis rat model of renal transplantation and a subset of human transplant Glomerulopathy. Transplantation. 2016;100(5):1004–14.
Dobrin RS, Day NK, Quie PG, Moore HL, Vernier HL, Michael AF, et al. The role of complement, immunoglobulin and bacterial antigen in coagulase-negative staphylococcal shunt nephritis. Am J Med. 1975;59(5):660–73.
Black JA, Challacombe DN, Ockenden BG. Nephrotic syndrome associated with bacteraemia after shunt operations for hydrocephalus. Lancet Lond Engl. 1965;2(7419):921–4.
Schoenbaum SC, Gardner P, Shillito J. Infections of cerebrospinal fluid shunts: epidemiology, clinical manifestations, and therapy. J Infect Dis. 1975;131(5):543–52.
Stickler GB, Shin MH, Burke EC, Holley KE, Miller RH, Segar WE. Diffuse glomerulonephritis associated with infected ventriculoatrial shunt. N Engl J Med. 1968;279(20):1077–82.
Strife CF, McDonald BM, Ruley EJ, McAdams AJ, West CD. Shunt nephritis: the nature of the serum cryoglobulins and their relation to the complement profile. J Pediatr. 1976;88(3):403–13.
Wakabayashi Y, Kobayashi Y, Shigematsu H. Shunt nephritis: histological dynamics following removal of the shunt. Case report and review of the literature. Nephron. 1985;40(1):111–7.
Larsen CP, Messias NC, Walker PD, Fidler ME, Cornell LD, Hernandez LH, et al. Membranoproliferative glomerulonephritis with masked monotypic immunoglobulin deposits. Kidney Int. 2015;88(4):867–73.
RUM receives funding from the German Research Foundation (DFG) and the Ministry of Science Northrine-Westfalia (MIWF). JUB receives funding from the DFG. No external funding source was involved in the design and writing of this case report.
Ethics approval and consent to participate
Ethics approval not applicable since the manuscript is a case report. Written consent was obtained and a copy of written consent is available upon request.
Consent for publication
Written informed consent was obtained from the participant for publication of this case report and any accompanying tables/images. A copy of the written consent is available for review by the Editor of this journal.
The authors declare that they have are no competing interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Völker, L.A., Burkert, K., Scholten, N. et al. A case report of recurrent membranoproliferative glomerulonephritis after kidney transplantation due to ventriculoatrial shunt infection. BMC Nephrol 20, 296 (2019). https://doi.org/10.1186/s12882-019-1472-1
- Shunt nephritis
- Membranoproliferative glomerulonephritis
- Kidney transplantation