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Combined bisalbuminemia and Bisalbuminuria: A rare finding on serum and urine electrophoresis.
Badr, Heba; Young, Paul E; Dong, Jianli; Okorodudu, Anthony O.
Afiliación
  • Badr H; Department of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
  • Young PE; Department of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
  • Dong J; Department of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
  • Okorodudu AO; Department of Pathology, University of Texas Medical Branch, Galveston, TX, United States. Electronic address: aookorod@utmb.edu.
Clin Chim Acta ; 552: 117635, 2024 Jan 01.
Article en En | MEDLINE | ID: mdl-37952813
ABSTRACT

BACKGROUND:

Bisalbuminemia and bisalbuminuria are rarely encountered serum and urine albumin anomalies characterized by the presence of a bifid albumin band on serum/urine protein electrophoresis (SPE/UPE) and serum/urine immunofixation electrophoresis (SIFE/UIFE). They are usually detected incidentally while screening for monoclonal gammopathy with a cumulative frequency of 11,000---110,000. CASE REPORT We report two cases of bisalbuminemia in two adult male diabetic patients. The first patient had a history of rheumatoid arthritis and strong clinical suspicion for Sjogren syndrome. The SPEP/UPEP and SIFE/UIFE in this patient showed combined bisalbuminemia and bisalbuminuria. While the second patient had chronic kidney disease due to nephrotic syndrome but showed bisalbuminemia alone.

CONCLUSION:

Bisalbuminemia and bisalbuminuria are rare findings with few case reports available in the English literature. These findings may occur secondary to inherited albumin variants or may be acquired. Diabetes mellitus is the medical condition most associated with acquired bisalbuminemia and bisalbuminuria. Although most cases of bisalbuminemia and bisalbuminuria are clinically insignificant, some albumin variants may have altered affinity for steroid hormones (e.g., thyroxine) and/or drugs which potentially could be clinically significant.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Gammopatía Monoclonal de Relevancia Indeterminada / Síndrome Nefrótico Límite: Adult / Humans / Male Idioma: En Revista: Clin Chim Acta Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Gammopatía Monoclonal de Relevancia Indeterminada / Síndrome Nefrótico Límite: Adult / Humans / Male Idioma: En Revista: Clin Chim Acta Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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