Autohemolysis and other changes resulting from the incubation in vitro of red cells from patients with congenital hemolytic anemia.
نویسندگان
چکیده
By ,J. C. SELW YN, M.I). (CANTAB.) AND .J. V. 11 cIE, MI)., M.ILC.P. (LoND.) T HE INCUBATION at 37 C. of sterile defibrimmated blood from cases of hereditary spherocyt.osis result.s iii a more rapid immcrease in osmotic fragility of the m’ed (.ellsm2. 22 amid a more rapid rate of autohemolysis3 ‘ thani normal. The cause of these unusually rapid changes lies in the m’ed (‘ells anm(l nmot mm the serum, as replacememit of the patient’s serum by salimme or by serum fm’om a normal personm does not retard the changes.3’ 12 Moreo ’ei’, artificial (‘oncenmtm’atioml of the blood causes a further inicrease mi both fragility and hemolysis.tm2 The beneficial results of splemiectomy mm hereditary spherocytosis immdicate without anmy doubt that the patient’s spleemi is of major importance in the causation of hemolysis in \‘i\.o. However, the exact mechammism of hemolysis is still not knowmm. Histologic
منابع مشابه
Atypical autohemolysis in hereditary spherocytosis as a reflection of two cell populations: relationship of cell lipids to conditioning by the spleen.
H EREDITARY SPHEROCYTOSIS is characterized by the occurrence of a hemolytic anemia in at least two family members, the presence of spherocytes in the peripheral blood, increased osmotic fragilities of fresh and incubated blood, an increased autohemolysis partially corrected by supplementary glucose and complete clinical remission following splenectomy. Several cases lacking one of these major f...
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متن کاملStudies on spontaneous in vitro autohemolysis in hemolytic disorders.
El) BLOOD CELLS from patiemits with hereditary spherocytosis (HS) and certaimi other hemolytic disorders umidergo lysis more readily than normal cells w’hemi incubated in vitro at body temperature for periods of 24 to 96 hours. Measurement of such spontaneous hemolysis, called “autohemolysis,” frequently aids in demonstrating abnormality of red cells, especially in cases of hereditary spherocyt...
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عنوان ژورنال:
- Blood
دوره 9 5 شماره
صفحات -
تاریخ انتشار 1954