scholarly journals A case of diagnosis of light chain proximal tubulopathy in a kidney transplant patient

2021 ◽  
Vol 5 ◽  
pp. 88-94
Author(s):  
T.A. Garkusha ◽  
◽  
E.A. Bykhanova ◽  
S.V. Gappoev ◽  
V.A. Khorzhevskii ◽  
...  

Light chain proximal tubulopathy (LCPT) is a disease characterised by accumulation of monoclonal immunoglobulins produced by tumour clones of plasma cells or B-lymphocytes in the epithelium of proximal renal tubules. One of LCPT forms is the crystal one, against the background of which epithelium of proximal renal tubules accumulates crystal structures of different sizes and shapes. This work presents an observation of a kidney transplant patient with crystal LCPT. The patient was admitted with azotaemia and underwent renal biopsy in order to establish the diagnosis. Morphological analysis drew attention to necrosis of epithelium of proximal renal tubules. Electron microscopy visualised crystal structures, immunohistochemical analysis of which revealed their monotypy in relation to lambda light chains of immunoglobulins. LCPT was diagnosed based on the comparison of the morphological picture and clinical data.

2021 ◽  
Vol 156 (Supplement_1) ◽  
pp. S154-S154
Author(s):  
A M Alkashash ◽  
C L Phillips

Abstract Introduction/Objective Patients with dysproteinemias may show a spectrum of renal alterations due to organized deposits of excess immunoglobulins, including primary amyloidosis, myeloma cast nephropathy, monoclonal immunoglobulin deposition disease, and light chain proximal tubulopathy (LCPT). Among the least common is LCPT, which shows ultrastructural cytoplasmic light chain inclusions with crystalline morphology or rarely fibrillar aggregates. We present the case of a patient with LCPT with fibrillar aggregates that is the only such case registered in our large academic surgical pathology electronic database. Our aim is to increase understanding and recognition of this rare variant. Methods/Case Report A 73-year-old man presented with 540 mg/day proteinuria, serum creatinine 5.73 mg/dL, platelets 178,000/cc, and 20% plasma cells in his bone marrow biopsy specimen. Kidney needle biopsy cores examined by light, fluorescent and transmission electron microscopy (EM) showed kappa light chain cast nephropathy and kappa LCPT with fibrillary aggregates, the latter requiring unmasking of kappa epitopes using pronase-treated paraffin sections. Congo red stain was negative. By EM, proximal tubules contained intracellular bundles of tightly aggregated fibrils with mean fibril diameter of 7.7 +/- 1.6 nm. Individual bundles were variably shaped as round, oval, spicular or irregular blobs. Fibrils were not seen in glomeruli. Results (if a Case Study enter NA) NA Conclusion This rare presentation of LCPT with fibrillar aggregates reinforces the utility of renal biopsy diagnosis that includes careful ultrastructural examination of renal tubules. In the absence of EM, the unique fibrillar organization of these cytoplasmic light chain aggregates would otherwise go unrecognized.


2020 ◽  
Vol 4 (1-2) ◽  
pp. 59-63 ◽  
Author(s):  
Elena V Zakharova ◽  
Tatyana A Makarova ◽  
Ekaterina S Stolyarevich ◽  
Olga A Vorobyeva ◽  
Irina G Rekhtina

Introduction: According to the recent International Kidney and Monoclonal Gammopathy Research Group Consensus report, the spectrum of monoclonal gammopathies of renal significance merges more than 12 conditions; and combinations of various patterns of monoclonal gammopathies of renal significance–associated kidney damage have already been described. We present a case of a previously unreported combination of C3 glomerulopathy and light-chain proximal tubulopathy. Case description: A 53-year-old Caucasian man presented with general weakness. Three years prior, a check-up revealed proteinuria and microhematuria, later accompanied by arterial hypertension, elevated serum creatinine, and a low serum C3 levels. On admission, his creatinine was 1.5 mg/dL; his protein excretion was 1900 mg/24 h with microhematuria at 150 hpf. His serum C3 was 79 mg/dL with a normal C4 level. Serum protein electrophoresis revealed an M-spike, immunochemistry confirmed monoclonal immunoglobulin G kappa secretion of 920 mg/dL, and traces of Bence–Jones protein kappa in his urine. A kidney biopsy showed mesangial hypercellularity with diffuse fine granular C3 mesangial expression and tubular atrophy with diffuse coarse granular kappa light-chain tubular epithelial cytoplasmic expression. Computed tomography did not reveal any destructive lesions. A bone marrow smear showed 5% plasma cells, and bone marrow cell flow cytometry demonstrated 87.4% of plasma cells with an aberrant phenotype. The patient was diagnosed with an monoclonal gammopathy of renal significance and administered bortezomib–cyclophosphamide–dexamethasone. After four courses, his monoclonal immunoglobulin G kappa secretion halved, but his serum creatinine and proteinuria remained almost unchanged. Chemotherapy was switched to lenalidomide–dexamethasone, and after five courses his immunoglobulin G kappa secretion decreased to traces, Bence–Jones protein was not observed and his urinalysis, serum creatinine, and C3 levels were detected as normal. Conclusion: The combination of kidney damage patterns, one of which was directly and the other indirectly associated with monoclonal gammopathy, complements the monoclonal gammopathies of renal significance spectrum. Chemotherapy led to a very good partial response and kidney function recovery.


2020 ◽  
Vol 35 (6) ◽  
pp. 899-904 ◽  
Author(s):  
Umberto Maggiore ◽  
Daniel Abramowicz ◽  
Marta Crespo ◽  
Christophe Mariat ◽  
Geir Mjoen ◽  
...  

2000 ◽  
Vol 34 (4) ◽  
pp. 536-536 ◽  
Author(s):  
María Outeda Macías ◽  
Pilar Salvador ◽  
Juan L Hurtado ◽  
Isabel Martín

2021 ◽  
Vol 6 (4) ◽  
pp. S314-S315
Author(s):  
G. GEMBILLO ◽  
F. D'Ignoto ◽  
P. Salis ◽  
D. Santoro ◽  
R. Liotta ◽  
...  

2006 ◽  
Vol 6 ◽  
pp. 412-528 ◽  
Author(s):  
Christine Wu ◽  
Parmjeet Randhawa ◽  
Jerry McCauley

BK virus is ubiquitously present in the latent state in humans, and awareness of the importance of BK polyomavirus is emerging among the kidney transplant community. First discovered in 1971 in the urine of a renal transplant recipient, BK virus nephropathy (BKVN) has come to be recognized as a significant cause of genitourinary disease and potential graft loss in the kidney transplant patient. In this review, we discuss the risk factors, available methods of diagnosis and therapeutic monitoring, and current approaches to therapy of BKVN.


2002 ◽  
Vol 97 (5) ◽  
pp. 751-753 ◽  
Author(s):  
Célia MF Gontijo ◽  
Raquel S Pacheco ◽  
Fernando Oréfice ◽  
Euler Lasmar ◽  
Eduardo S Silva ◽  
...  

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