Plasma cell dyscrasia : LCDD vs immunotactoid glomerulopathy

Joint Authors

Jabbur, Wail Latif
Khalil, Abd Allah
Said, Harith M.

Source

Saudi Journal of Kidney Diseases and Transplantation

Issue

Vol. 19, Issue 5 (31 Oct. 2008), pp.802-805, 4 p.

Publisher

Saudi Center for Organ Transplantation

Publication Date

2008-10-31

Country of Publication

Saudi Arabia

No. of Pages

4

Main Subjects

Medicine

Topics

Abstract EN

Light chain deposit disease is a plasma cell disorder characterized by production of a large amount of monoclonal immunoglobulin light chain or part of it, which is usually deposited as an amorphous substance in the kidneys.

Immunotactoid glomerulopathy is an uncommon disease, which might be related to plasma cell dyscrasia, and characteristically manifest as organized glomerular ultra structural fibrils or microtubules.

In this article, we report a case of a combined presentation of light chain disease and immunotactoid glomerulopathy in a patient with multiple myeloma and reversible advanced renal failure.

American Psychological Association (APA)

Jabbur, Wail Latif& Said, Harith M.& Khalil, Abd Allah. 2008. Plasma cell dyscrasia : LCDD vs immunotactoid glomerulopathy. Saudi Journal of Kidney Diseases and Transplantation،Vol. 19, no. 5, pp.802-805.
https://search.emarefa.net/detail/BIM-39786

Modern Language Association (MLA)

Jabbur, Wail Latif…[et al.]. Plasma cell dyscrasia : LCDD vs immunotactoid glomerulopathy. Saudi Journal of Kidney Diseases and Transplantation Vol. 19, no. 5 (Dec. 2008), pp.802-805.
https://search.emarefa.net/detail/BIM-39786

American Medical Association (AMA)

Jabbur, Wail Latif& Said, Harith M.& Khalil, Abd Allah. Plasma cell dyscrasia : LCDD vs immunotactoid glomerulopathy. Saudi Journal of Kidney Diseases and Transplantation. 2008. Vol. 19, no. 5, pp.802-805.
https://search.emarefa.net/detail/BIM-39786

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references : p. 805

Record ID

BIM-39786