Minimal change nephrotic syndrome in a patient with strongyloidiasis
β Scribed by Mieko Miyazaki; Masahito Tamura; Narutoshi Kabashima; Ryota Serino; Tatsuya Shibata; Tetsu Miyamoto; Yumi Furuno; Tetsuo Nishio; Jiro Ohara; Toshihiro Sakurai; Yutaka Otsuji
- Publisher
- Springer
- Year
- 2010
- Tongue
- English
- Weight
- 366 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1342-1751
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Serum levels of IgE were studied in 30 children with minimal-change nephrotic syndrome and 32 children with mesangioproliferative glomerulonephritis during different stages of the disease and treatment. In addition, tissue obtained by renal biopsy was investigated by immunofluorescence histology; no
Glomerular lesions have rarely been reported with angioimmunoblastic lymphadenopathy (AILD). A patient with histologically documented AILD developed the nephrotic syndrome. Renal biopsy demonstrated minimal change disease. Both the lymphadenopathy and the nephrotic syndrome spontaneously remitted in