Multisite distribution of fibrillary inclusions in a patient with light chain proximal tubulopathy: A case report

Author:

Wang Yingying1,Chen Kai1,Zhou Shengguo1,Zhang Wei1ORCID

Affiliation:

1. Department of Nephrology, Jining No. 1 People’s Hospital, Jining, Shandong, China.

Abstract

Rationale: Light chain proximal tubulopathy (LCPT) is a rare form of renal impairment associated with multiple myeloma (MM). LCPT is caused by inclusions formed of free light chains that are typically crystalline, but can also be noncrystalline structures. Patient concerns: A 62-year-old man was hospitalized for the investigation of abnormal urine test results lasting for 1 year and kidney-function abnormalities persisting for more than 1 month. Diagnoses: Noncrystalline LCPT and MM. Interventions: The patient was treated with the lenalidomide, bortezomib, and dexamethasone and pomalidomide, bortezomib, and dexamethasone chemotherapy regimens. Outcomes: Complete remission of MM was achieved, and the patient’s renal function returned to normal. Lessons: This case report highlights the importance of renal pathology in the diagnosis of patients with unexplained chronic kidney disease and proteinuria.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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