SINCE the report of Rathery1 in 1902, many cases of leukoerythroblastic anemia associated with myelofibrosis and myeloid metaplasia of the spleen have been described. This syndrome has been designated by a variety of descriptive terms, among which "agnogenic myeloid metaplasia"2 has been popular in recent years. The subject has been extensively reviewed by several authors.3 4 5 Donhauser,6 in 1908, suggested that the disorder was brought about by a primary depression of bone-marrow function, possibly resulting from toxic or other untoward influences, and that extramedullary blood formation occurred in the spleen and liver as a compensatory reaction. In 1937 Hickling3 first called . . .
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Green et al. (1953) studied this question.
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