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Acute yellow atrophy of the liver
Excerpt from article by G. Bruton Sweet, M.B., published
in NZMJ 1911 May:11(42):141–142.
Acute Yellow Atrophy must be ranked among the rarest of
diseases. According to Hunter, it is seldom met with in the largest hospital
practice. Out of 25,700 cases admitted during nine years into the London Fever
Hospital at a time when a brown tongue and delirium constituted a sure passport
to admission, Murchison only met with one case.
Although observed as early as the year 1616, Best in 1903
estimated that the total number of records d cases did not exceed 500 in number.
Rare as this disease is in adult life—the great bulk of cases on record
are in female adults between the age of 20 and 40 years—it is still more
uncommon in children, although no age is exempt. Of 343 cases collected by
English and Continental authorities, only 21 were in children under the age of
10. In America some years ago Heyes collected 17 cases, including one of his
own, the youngest being only three months old.
The disease in children presents the same symptoms and runs
the same course as in adult life. At the onset, it cannot be distinguished from
simple catarrhal jaundice. Icterus, nausea or vomiting, general malaise, with
some enlargement of the liver and clay-coloured stools present a group of
symptoms commonly associated with this mild disorder. After a period of from one
to eight weeks from the onset, however, grave signs appear—extreme
restlessness, delirium, and widely dilated pupils point to some severe cerebral
disturbance ; vomiting becomes persistent, and the vomit often becomes black or
coffee ground in appearance.
Examination of the abdomen shows all extraordinary
diminution or even entire absence of the usual liver dullness, and a
microscopical examination of the urine in a certain percentage of cases reveals
crystals of leucin or tyrosin or both. In the great majority of cases the
patient rapidly loses ground, becomes comatose, and the disease has a fatal
termination; only very few apparently authentic cases having been recorded of
ultimate complete recovery.
Recently a case of this disease was observed by me in the
Auckland Hospital, and the symptoms during life and the morbid condition of the
liver and other organs discovered at the autopsy were typical of acute yellow
atrophy.
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