Editorial
Neurology of Whipple's disease
| The first 150 words of the full text of this article appear below. |
In
1907, George Hoyt Whipple, then an instructor in pathology at Johns
Hopkins University, published a case report of a 36 year old physician
who had been domiciled in Constantinople.1 He developed
recurring arthropathy, weight loss, and steatorrhoea, became worse, and
died. At necropsy the intestine and mesenteric lymph glands were
infiltrated by mononuclear and polynuclear giant cells and deposits of
fat and fatty acids. Whipple described the large "foamy"
mononuclear cells in the intestinal mucosa which were later shown to
contain periodic acid Schiff (PAS) positive material. The aetiology of
the condition was not established and he wrote "Gland tissue treated
by the Levaditi method shows great numbers of a peculiar rod-shaped
organism (?) which does not stain by the aniline dyes . . ." Whether this is the aetiological factor in this disease
cannot be determined from this case". A prescient observation. He
suggested intestinal lipodystrophy as a name for the
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