| Literature DB >> 17170630 |
Kirk M Chan-Tack1, Navneet Ahuja, Edward J Weinman, Ravinder K Wali, Anayochukwu Uche, Lisa A Greisman, Cinthia Drachenberg, Philip N Hawkins, Robert R Redfield.
Abstract
Amyloidosis is an uncommon cause of renal disease in HIV-positive patients. Diagnosis is challenging, treatment options are limited, and prognosis remains poor. We discuss an HIV-positive patient with acute renal failure and nephrotic range proteinuria. The differential diagnosis included nephropathy due to trimethoprim/sulfamethoxazole, tenofovir, HIV, hepatitis C, heroin, or multifactorial causes. Serum and urine study findings were inconclusive. Rapid clinical deterioration ensued and a renal biopsy was performed. Pathologic examination revealed eosinophilic, amorphous material in the glomerular tufts that stained red-orange with Congo red stain. Immunohistochemical analysis confirmed amyloid A (AA) amyloidosis. AA amyloidosis occurs as a complication of chronic infection or chronic inflammatory disease. It has been reported in intravenous or subcutaneous drug abusers, some of whom were HIV-positive. This case underscores the importance of tissue diagnosis to determine the cause of renal disease in HIV-positive patients. Clinical diagnosis, based on CD4 count, viral load, and degree of proteinuria, may not predict the pathological diagnosis in HIV-positive patients.Entities:
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Year: 2006 PMID: 17170630 DOI: 10.1097/00000441-200612000-00012
Source DB: PubMed Journal: Am J Med Sci ISSN: 0002-9629 Impact factor: 2.378