MALADIE DE WALDMANN PDF

La maladie de Waldmann (lymphangiectasies intestinales primitives) est responsable d’une entéropathie exsudative par fuite de la lymphe dans la lumière. Very rare familial forms of Waldmann’s disease have been reported [1,4]. Go to: .. Vignes S. Lymphangiectasies intestinales primitives (maladie de Waldmann) . Publication – Article. Lymphangiectasies intestinales primitives (maladie de Waldmann). La Revue de Médecine Interne, 39(7), ,

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L’examen histologique du nodule confirmait le diagnostic de maladie de Kimura. Kimura’s disease is a rare and benign chronic inflammatory soft-tissue disorder of unknown origin.

Most cases involve young Waldann males. The typical presentation consists of painless papules or nodules with a predilection for the head and neck region, associated with lymphadenopathy, parotid gland involvement, peripheral blood eosinophilia and raised immunoglobulin E.

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Primary intestinal lymphangiectasia (Waldmann’s disease)

A year-old Mauritian man was hospitalized for nephrotic syndrome. Histopathologic examination of a nodule confirmed the diagnosis of Kimura’s disease, which was associated with necrotic extracapillary glomerulonephritis. Corticosteroids were initiated, resulting in rapid improvement of renal function and partial regression of the patient’s cutaneous nodules and lymph node disorder.

Many different histologic types of renal involvement may be observed with potentially severe lesions. To our knowledge, this is the first case of Kimura’s disease associated with extracapillary glomerulonephritis.

Lymphangiectasies intestinales primitives (maladie de Waldmann) – Dimensions

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Waldmann disease

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