Membranous nephropathy associated with multicentric Castleman’s disease that was successfully treated with tocilizumab: a case report and review of the literature

Abstract

Background

Multicentric Castleman’s disease is a life-threatening disorder involving a systemic inflammatory response and multiple organ failure caused by the overproduction of interleukin-6. Although renal complications of Castleman’s disease include AA amyloidosis, thrombotic microangiopathy, and membranoproliferative glomerulonephritis, membranous nephropathy is relatively rare. We experienced a case of secondary membranous nephropathy associated with Castleman’s disease.

Case presentation

The patient was a 43-year-old Japanese man who had shown a high zinc sulfate value in turbidity test, polyclonal hypergammaglobulinemia, anemia, and proteinuria. A physical examination revealed diffuse lymphadenopathy, an enlarged spleen and papulae of the body trunk. A skin biopsy of a papule on the patient’s back showed plasma cells in the perivascular area and he was diagnosed with multicentric Castleman’s disease, plasma cell variant. Kidney biopsy showed the appearance of bubbling in the glomerular basement membranes in Periodic acid methenamine silver stain and electron microscopy revealed electron dense deposits within and outside the glomerular basement membranes. Since immunofluorescence study showed predominant granular deposition of IgG1 and IgG2, he was diagnosed with secondary membranous nephropathy associated with Castleman’s disease. He was initially treated with prednisolone alone, however his biochemical abnormalities did not improve. After intravenous tocilizumab (700 mg every 2 weeks) was started, his C-reactive protein elevation, anemia, and polyclonal gammopathy improved. Furthermore, his urinary protein level declined from 1.58 g/gCr to 0.13 g/gCr. The prednisolone dose was gradually tapered, then discontinued. He has been stable without a recurrence of proteinuria for more than 6 months.

Conclusions

Tocilizumab might be a treatment option for secondary membranous nephropathy associated with Castleman’s disease.

Background

Castleman’s disease (CD) consists of a lymphoproliferative disorder that was first reported by Castleman et al. [1]. CD is classified into two types: unicentric CD (UCD) and multicentric CD (MCD). While UCD is thought to be a benign disease because curative resection is possible for most patients [2], MCD is a life-threatening disorder involving a systemic inflammatory response and multiple organ failure caused by the overproduction of interleukin-6 (IL-6) [3]. Previous studies have shown that renal complications of CD mainly include AA amyloidosis, thrombotic microangiopathy (TMA), and membranoproliferative glomerulonephritis (MPGN) [4, 5]. The treatment of renal complications of CD has not been clarified. We herein report a case of secondary membranous nephropathy (MN) associated with CD that was successfully treated with tocilizumab.

Case presentation

The patient was a 43-year-old Japanese man who had shown a high zinc sulfate value in turbidity test in a health checkup 4 years previously. He was examined by a local doctor who pointed out hypergammaglobulinemia and anemia. He had taken colchicine and febuxostat to treat gout 3 years previously. After presenting mild hematuria and proteinuria 2 years previously, he was referred to our hospital for further examination and treatment. The patient’s height was 170 cm, and his body weight was 85 kg. His blood pressure was 129/83 mmHg, his pulse was 95 beats/minute, and his body temperature was 36.2 °C. He sometimes experienced night sweat. A physical examination revealed diffuse lymphadenopathy, an enlarged spleen and papulae of the body trunk. The laboratory data are shown in Table 1. There was no monoclonal peak on immunoelectrophoresis in serum and urine tests. Renal ultrasound showed that the kidneys were of normal size, with normal renal arterial resistive indices. Computed tomography of the chest, abdomen, and pelvis showed cervical, axillary, and paraaortic lymphadenopathies and splenomegaly.

Table 1 Laboratory data before the kidney biopsy

An excisional submental lymph node biopsy showed diffuse interfollicular plasma cell infiltration (Fig. 1a). Immunohistochemistry revealed neither interfollicular plasmacytosis nor laterality of the κ or λ light chains. IgG4-positive cells were detected, but the IgG4/IgG ratio was < 0.1. A skin biopsy of a papule on the patient’s back showed plasma cells in the perivascular area (Fig. 1b). The patient was diagnosed with MCD, plasma cell variant.

Fig. 1

Light microscopy. a A submental lymph node biopsy showed diffuse interfollicular plasma cell infiltration (Hematoxylin and eosin staining [HE]). Left panel: Bar = 50 μm, Right panel: Bar = 50 μm. b Skin biopsy showed plasma cells in the perivascular area (HE). Left panel: Bar = 250 μm, Right panel: Bar = 100 μm. c Kidney biopsy findings. HE staining showed no sign of inflammatory cell infiltration in the glomeruli. Periodic acid Schiff (PAS) staining showed no signs of mesangial proliferation, crescents, or adhesion. Periodic acid methenamine silver (PAM) staining showed the appearance of bubbling (enlarged rectangle) in the glomerular basement membranes. Masson-Trichrome (MT) staining showed no sign of immune complex deposits in the glomeruli. Bars = 50 μm

Kidney biopsy revealed 2 instances of global sclerosis in 19 glomeruli. Hematoxylin and eosin (HE) staining showed that there was no inflammatory cell infiltration in the glomeruli (Fig. 1c). Periodic acid Schiff (PAS) staining showed no signs of mesangial proliferation, crescents, or adhesion (Fig. 1c). Periodic acid methenamine silver (PAM) staining showed the appearance of bubbling in the glomerular basement membranes (Fig. 1c). Masson-Trichrome (MT) staining demonstrated the absence of immune complex deposits in the glomeruli (Fig. 1c). Immunofluorescence showed the focal granular deposition of IgG and C3 along the glomerular basement membranes (Fig. 2a). The IgG deposits were predominantly composed of IgG1 and IgG2, but not IgG4, suggesting secondary MN rather than primary MN (Fig. 2b). Anti-phospholipase A2 receptor antibodies were not measured. There was no big difference in staining between κ and λ chains (Fig. 2b). Direct fast scarlet staining was negative. Electron microscopy revealed electron dense deposits within and outside the glomerular basement membranes (Fig. 3). Based on these results, the patient was diagnosed with secondary MN.

Fig. 2

Immunofluorescence study. a Immunofluorescence showed strong focal granular staining for IgG and weak focal granular staining for C3 along the glomerular basement membranes. Immunofluorescence showed no signs of IgA, IgM, C1q or Fib. Bars = 50 μm. b IgG subclass staining was composed of predominantly IgG1 and IgG2, not IgG4. Bars = 50 μm. There was no major difference in staining between the κ and λ chains. Bars = 50 μm

Fig. 3

Electron microscopy. Electron dense deposits were observed within glomerular basement membranes. This was classified as Ehrenreich-Churg stage III. Bar = 2 μm

The patient was initially treated with prednisolone alone; however, his biochemical abnormalities did not improve. Thus, intravenous tocilizumab (700 mg every 2 weeks) was started. After treatment with tocilizumab, the patient’s C-reactive protein (CRP) elevation, anemia, and polyclonal gammopathy improved (Fig. 4). Furthermore, his urinary protein level declined from 1.58 g/gCr to 0.13 g/gCr. The prednisolone dose was gradually tapered, then discontinued. He has been stable without a recurrence of proteinuria for more than 6 months.

Fig. 4

The clinical course

Discussion and conclusions

We experienced a rare case of MN that was associated with MCD. The patient’s high zinc sulfate level was considered to be related to CD. In a kidney biopsy specimen, PAM staining revealed a bubbling appearance in the glomerular basement membranes and electron microscopy revealed electron dense deposits within and outside the glomerular basement membranes; these findings were compatible with a diagnosis of MN. Since the IgG depositions were predominantly composed of IgG1 and IgG2, the MN in the present case was thought to be secondary rather than primary.

Regarding renal complications of CD, 9–71% of CD patients are reported to have elevated creatinine or blood urea nitrogen [6]. Another report showed that 19 of 76 CD patients (25%) had renal involvement and that the most common etiology was TMA-like lesions [7]. Several studies reported that the renal histology of CD mainly included AA amyloidosis, TMA, and MPGN [4, 5]. CD-associated AA amyloidosis might be caused by the overproduction of IL-6 because IL-6 was reported to play a critical role in the synergistic induction of the human SAA gene [8]. With respect to CD-associated renal TMA, Mutneja et al. reported that the VEGF expression in podocytes was decreased despite there being a high level of VEGF in circulation [9]. Since the local reduction of VEGF within the kidney was reported to be sufficient to trigger the pathogenesis of TMA in adult mice [10], CD-associated renal TMA might be caused by the downregulation of VEGF in podocytes. Regarding CD-associated MPGN, the exact mechanism through which CD leads to MPGN remains unknown; however, MPGN related to CD might be secondary to chronic TMA [11].

We searched the PubMed database for relevant studies using the following search term: “castleman kidney” or “castleman membranous nephropathy” or “membranous nephropathy angiofollicular lymph node hyperplasia”. CD-associated MN was rare, in addition to the present case, only 7 cases were identified in the relevant English literature (Table 2) [7, 12,13,14,15,16,17]. Among the 8 reported cases (including the present case), seven patients were male; only one patient was female. All patients who were tested had high serum levels of VEGF, IL-6, and CRP. Six patients experienced proteinuria. The histopathological patterns of the 8 cases were as follows: hyaline-vascular (HV) type, n = 2; plasma-cell type, n = 3; mixed type, n = 1; and unknown type, n = 2 (Table 3). Six of the 8 cases had favorable renal outcomes. Only case 1 experienced acute kidney injury, resulting in chronic renal failure. The treatment options varied.

Table 2 Summary of reported cases of membranous nephropathy associated with Castleman’s disease

Table 3 Summary of the outcomes of the reported cases

Previous reports suggested the efficacy of tocilizumab in reducing proteinuria as a renal complication of CD [14, 17, 18]. There were three cases of MN caused by CD, including the present case, that were treated with tocilizumab (Table 3). Komaba et al. [14]. reported a case of mixed-type CD that was treated with tocilizumab while the case reported by Furutera et al. [17] and the present case were plasma cell-type CD. Although it has not been clarified why CD causes MN, the reduction of proteinuria in CD-associated MN by tocilizumab, which is an IL-6 receptor antagonist, suggests that CD-associated MN might be related to IL-6. While he has been stable without recurrence of proteinuria for more than 6 months, a longer follow-up period is needed, as the proteinuria in the present case previously became exacerbated 5 months after treatment with tocilizumab.

In conclusion, we experienced a case of CD-associated MN in which tocilizumab was effective for reducing proteinuria. Further reports should be accumulated to determine why patients with CD can present secondary MN as a renal complication, and why tocilizumab can reduce proteinuria in CD-associated MN.