Chronic Erythrocytic Hypoplasia following Pernicious Anemia.

نویسندگان

  • C GOLDSTEIN
  • L PECHET
چکیده

C HRONIC ERYTHROCYTIC HYPOPLASIA in adults is a rare entity.’ It was described for the first time in 1922,2 as a progressive normochromic anemia with erythropoietic aplasia of the bone marrow, reticulocytopenia, normal leukopoiesis and thrombopoiesis, and absence of enlarged spleen or lymph nodes. Infections,3 drugs,4 immunologic reactions,5 azotemia,6’ thymic tumors,8’#{176} and an inborn error of metabolism’0 have all been implicated as conditioning a selective impairment of the erythropoietic activity. The case to be reported, treated pernicious anemia followed by erythrocytic hypoplasia, presents a sequence we believe has not been previously described.

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عنوان ژورنال:
  • Blood

دوره 25  شماره 

صفحات  -

تاریخ انتشار 1965