WHIPPLE'S DISEASE - 09/09/11
Résumé |
In 1907, G. H. Whipple performed an autopsy on a 36-year-old physician “characterized by a gradual loss of weight and strength, stools consisting chiefly of neutral fat and fatty acids, indefinite abdominal signs, and a peculiar multiple arthritis.”20 He described “peculiar wandering and phagocytic mononuclear cells” in the intestinal walls and mesenteric lymph nodes as well as the presence of rod-like bacilli in the lamina propria of the intestine.5 The next case reported in the literature was in 1923. In 1949, Black-Schaffer1 demonstrated that the macrophages found in the intestinal mucosa of a patient with Whipple's disease stained vividly by the periodic acid–Schiff (PAS) method.
Using electron microscopy in 1961, Yardley et al revealed that these same rod-shaped structures in the intestinal mucosa and within the intestinal macrophages were bacteria. Later that year, the same group reported finding PAS-positive macrophages in tissue sections obtained from Whipple's original patient. Peroral small bowel biopsy was used in 1947 to make the first premortem diagnosis of this condition.5 In 1952, Paulley was the first to use antibiotics successfully to treat Whipple's disease, but it was recognized only subsequently that Whipple's disease is systemic in nature and can respond to a variety of antibiotic regimens.13 Although the disease was recognized as an infectious disease for decades, it was not until the 1990s that the causative organism was definitively identified and classified as Tropheryma whippelii.
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| Address reprint requests to Robert F. Boynton, MD, Allegheny University of the Health Sciences–, Medical College of Pennsylvania, 3300 Henry Avenue, Philadelphia, PA 19129 |
Vol 27 - N° 3
P. 683-695 - septembre 1998 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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