Literature DB >> 19550057

Renal amyloidosis secondary to childhood tuberculosis: a report of two cases.

S Krishnamurthy1, D Samanta, S Yadav.   

Abstract

Childhood renal amyloidosis is a rare entity and is mostly secondary in nature. We describe two cases of renal amyloidosis in association with childhood tuberculosis. The first case was a 10-year-old girl who presented with abdominal tuberculosis and nephrotic syndrome, while the second case was a 5-year-old boy who presented with disseminated tuberculosis and nephrotic syndrome. They were found to have amyloidosis on renal biopsy. The former was treated with anti-tubercular drugs, while the latter required anti-tubercular drugs and steroids. Both the cases showed clinical improvement with remission of nephrotic syndrome. Successful treatment of tuberculosis can result in remission of nephrotic syndrome due to secondary renal amyloidosis. It is important, especially in developing countries, to be aware that tuberculosis continues to be part of the differential diagnosis of amyloidosis in children.

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Year:  2009        PMID: 19550057     DOI: 10.4103/0022-3859.52843

Source DB:  PubMed          Journal:  J Postgrad Med        ISSN: 0022-3859            Impact factor:   1.476


  1 in total

1.  Amyloidosis in a child with leucocyte adhesion deficiency type-1: an unusual association.

Authors:  Amit Rawat; Surjit Singh; Dhrubajyoti Sharma; Deepti Suri; Arvind Rajwanshi; Amos Etzioni
Journal:  Indian J Pediatr       Date:  2011-05-08       Impact factor: 1.967

  1 in total

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