Klinische Wochenschrift · 1983
Chronic interstitial nephritis in Whipple's disease.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Schlumpf A, Marbet U A, Stöcklin E, Wegmann W, Lämmle B, Mujagic M, Jösch W, Thiel G, Thölen H, Olivieri W, Gudat F, Torhorst J, Zollinger H U, Mihatsch M J
Аннотация
Report is given on a 68-year-old man who suffered primarily from progressive weight loss and repeated episodes of fever and arthralgia. Later, liver dysfunction and renal insufficiency developed. Liver and kidney biopsies disclosed granulomatous hepatitis and nephritis. Because of the morphologic and clinical findings, the diagnosis of Boeck's disease was made. Shortly before death, diarrhea developed. Autopsy revealed a massive systemic involvement in Whipple's disease proven by light and electron microscopy and immunofluorescence. Tuberculoid and epitheloid cell granulomas and isolated giant cells were found in addition to the biopsy findings in skeleton muscles, the small intestine, lymphnodes and bronchi. At autopsy, the kidney showed chronic interstitial nephritis. The literature of kidney involvement in Whipple's disease is reviewed. This is the first case with granulomatous interstitial nephritis and chronic renal insufficiency in an inadequately treated Whipple's disease.