PMID- 27437235 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20160720 LR - 20200930 IS - 2249-782X (Print) IS - 0973-709X (Electronic) IS - 0973-709X (Linking) VI - 10 IP - 5 DP - 2016 May TI - Unusual Presentation of Light Chain Deposition Disease: A Case Report. PG - ED08-9 LID - 10.7860/JCDR/2016/18358.7762 [doi] AB - Light Chain Deposition Disease (LCDD) is a rare disease characterized by deposition of monoclonal non-amyloid light chains in multiple organs. We report an unusual histologic manifestation of LCDD in a 55-year-old female patient, who presented with nephrotic syndrome and an increased serum creatinine. This case of LCDD had features of cast nephropathy on biopsy which is diagnostic of myeloma kidney, when the patient was clinically asymptomatic. Serum electrophoresis showed no abnormal band. There was no other evidence of a B-cell clonal disorder or amyloidosis. Following chemotherapy, improvement in renal function correlated with a reduction in circulating light-chain levels. FAU - Arora, Disha AU - Arora D AD - Senior Resident, Department of Pathology, Safdarjung Hospital , New Delhi, India . FAU - Uppal, Mayank AU - Uppal M AD - Ex- Senior Resident, Department of Medicine, Safdarjung Hospital , New Delhi, India . FAU - Amitabh, Vindu AU - Amitabh V AD - Head of Department, Department of Nephrology, Safdarjung Hospital , New Delhi, India . FAU - Agrawal, Usha AU - Agrawal U AD - Scientist E, National Institute of Pathology, Safdarjung Hospital Campus , New Delhi, India . LA - eng PT - Case Reports DEP - 20160501 PL - India TA - J Clin Diagn Res JT - Journal of clinical and diagnostic research : JCDR JID - 101488993 PMC - PMC4948411 OTO - NOTNLM OT - Cast nephropathy OT - Myeloma kidney OT - Nephrotic syndrome EDAT- 2016/07/21 06:00 MHDA- 2016/07/21 06:01 PMCR- 2016/07/01 CRDT- 2016/07/21 06:00 PHST- 2015/12/15 00:00 [received] PHST- 2016/02/29 00:00 [accepted] PHST- 2016/07/21 06:00 [entrez] PHST- 2016/07/21 06:00 [pubmed] PHST- 2016/07/21 06:01 [medline] PHST- 2016/07/01 00:00 [pmc-release] AID - 10.7860/JCDR/2016/18358.7762 [doi] PST - ppublish SO - J Clin Diagn Res. 2016 May;10(5):ED08-9. doi: 10.7860/JCDR/2016/18358.7762. Epub 2016 May 1.