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KMID : 0381219930250010101
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Journal of RIMSK
1993 Volume.25 No. 1 p.101 ~ p.106
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A Case of Congenital Pelger-Huet Anomaly
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전정호
임인석/김철하/유병훈/채석래
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Abstract
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Congenital Pelger-Huet anomaly is characterized by a lack of segmentation and an increased chromatin condensation of granulocyte nuclei, It has been reported that an acquired, or "pseudo," morphologically similar defect occurs transiently in the
course
of a variety of hematologic and nonhematologic conditions including leukemoid reactions, myeloproliferative disorders and severe bacterial infection.
We report a case report of congenital Pelger-Huet anomaly is presented in a 8 year olds boy who was admitted with urticaria. His grandmother, father and aunt were revealed with PelgerHuet anomaly Their peripheral blood smear showed 90~94%
Pelger-Huet
anomaly in neutrophil.
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