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Association light chain deposition disease (LCDD) and amyloidosis. One case.
Pathol Res Pract. 1985 Aug; 180(2):214-9.PR

Abstract

Up to now, light chain deposition disease (L.C.D.D.) and amyloidosis have been shown to occur in different individuals. A case of association is described in a 76 year old man with terminal renal failure and normal size kidneys. Percutaneous renal biopsy showed glomerular and peritubular fixation of labeled antikappa light chain serum. Stains for amyloidosis were positive in small vessels. Kappa free chains were found in both serum and urine and the bone marrow showed predominantly kappa-containing plasma cells. By electron microscopy both electron-dense granular deposits and amyloid like fibrils were found in the wall of arterioles and small arteries.

Authors

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Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

3932985

Citation

Hofmann-Guilaine, C, et al. "Association Light Chain Deposition Disease (LCDD) and Amyloidosis. One Case." Pathology, Research and Practice, vol. 180, no. 2, 1985, pp. 214-9.
Hofmann-Guilaine C, Nochy D, Jacquot C, et al. Association light chain deposition disease (LCDD) and amyloidosis. One case. Pathol Res Pract. 1985;180(2):214-9.
Hofmann-Guilaine, C., Nochy, D., Jacquot, C., Tricottet, V., Bariety, J., & Camilleri, J. P. (1985). Association light chain deposition disease (LCDD) and amyloidosis. One case. Pathology, Research and Practice, 180(2), 214-9.
Hofmann-Guilaine C, et al. Association Light Chain Deposition Disease (LCDD) and Amyloidosis. One Case. Pathol Res Pract. 1985;180(2):214-9. PubMed PMID: 3932985.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Association light chain deposition disease (LCDD) and amyloidosis. One case. AU - Hofmann-Guilaine,C, AU - Nochy,D, AU - Jacquot,C, AU - Tricottet,V, AU - Bariety,J, AU - Camilleri,J P, PY - 1985/8/1/pubmed PY - 1985/8/1/medline PY - 1985/8/1/entrez SP - 214 EP - 9 JF - Pathology, research and practice JO - Pathol. Res. Pract. VL - 180 IS - 2 N2 - Up to now, light chain deposition disease (L.C.D.D.) and amyloidosis have been shown to occur in different individuals. A case of association is described in a 76 year old man with terminal renal failure and normal size kidneys. Percutaneous renal biopsy showed glomerular and peritubular fixation of labeled antikappa light chain serum. Stains for amyloidosis were positive in small vessels. Kappa free chains were found in both serum and urine and the bone marrow showed predominantly kappa-containing plasma cells. By electron microscopy both electron-dense granular deposits and amyloid like fibrils were found in the wall of arterioles and small arteries. SN - 0344-0338 UR - https://www.unboundmedicine.com/medline/citation/3932985/Association_light_chain_deposition_disease__LCDD__and_amyloidosis__One_case_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0344-0338(85)80177-1 DB - PRIME DP - Unbound Medicine ER -