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11. |
Initial alkylating agent chemotherapy in a leukemic hairy cell patient |
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American Journal of Hematology,
Volume 16,
Issue 1,
1984,
Page 91-94
Ellen Gaynor,
Harvey M. Golomb,
Jason McClellan,
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摘要:
AbstractA patient with moderate splenomegaly and the leukemic phase of hairy cell leukemia presented with a white blood cell count (WBC) of 85,600/mm3with 87% hairy cells and platelets of 125,000/mm3. Initial therapy consisted of chlorambucil alone at 4 mg each day. Within 6 months, the WBC decreased to 27,000/mm3with 82% hairy cells, and the spleen was not palpable; platelets remained at 142,000/mm3. The patient has continued to do well for 2 years since the start of therapy, requiring no transfusions and having no problems secondary to organ infiltration. Selected hairy cell patients, those with a significant leukemic phase and with only mild thrombocytopenia, may benefit from initial chlorambucil therapy rather than immediate splenectomy.
ISSN:0361-8609
DOI:10.1002/ajh.2830160112
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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12. |
Quinidine‐induced agranulocytosis |
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American Journal of Hematology,
Volume 16,
Issue 1,
1984,
Page 95-98
Saramma J. Alexander,
Robin I. Gilmore,
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摘要:
AbstractA case of agranulocytosis in an 86‐year‐old man after 8 weeks treatment with quinidine sulfate is described. Acute phase serum from the patient demonstrated antineutrophil activity by the microgranulocytotoxicity assay. Review of the literature reveals that more than one mechanism could cause this idiosyncratic immune‐mediated agranulocy
ISSN:0361-8609
DOI:10.1002/ajh.2830160113
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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13. |
Juvenile features in adult‐type chronic granulocytic leukemia |
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American Journal of Hematology,
Volume 16,
Issue 1,
1984,
Page 99-102
James C. Gay,
Emmanuel N. Dessypris,
James S. Roloff,
John N. Lukens,
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摘要:
AbstractPhiladelphia chromosome (Ph1) positive, or “adult‐type,” chronic granulocytic leukemia (CGL) differs in many clinical and laboratory aspects from PH1‐negative, or “juvenile,” CGL. Because of these differences, the disorders have been considered two distinct disease entities. We present a child with Ph1‐positive CGL whose disease has several features more characteristic of the Ph1‐negative syndrome. This case demonstrates that the chromosomal anomaly in CGL is not always predictive of phenotypic expression
ISSN:0361-8609
DOI:10.1002/ajh.2830160114
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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14. |
Erratum |
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American Journal of Hematology,
Volume 16,
Issue 1,
1984,
Page 103-103
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PDF (56KB)
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ISSN:0361-8609
DOI:10.1002/ajh.2830160116
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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15. |
Announcements |
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American Journal of Hematology,
Volume 16,
Issue 1,
1984,
Page 104-104
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PDF (45KB)
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ISSN:0361-8609
DOI:10.1002/ajh.2830160117
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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16. |
Masthead |
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American Journal of Hematology,
Volume 16,
Issue 1,
1984,
Page -
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PDF (101KB)
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ISSN:0361-8609
DOI:10.1002/ajh.2830160101
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1984
数据来源: WILEY
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