Idiopathic myelofibrosis mimicking hemolytic anemia

<p><span style="font-family: Calibri;">Idiopathic Myelofibrosis is an infrequent chronic myeloproliferative disorder characterized by varying degrees of bone marrow fibrosis and extra medullary hematopoiesis, with the fibrosis being a reactive phenomenon to a neoplastic prolife...

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Bibliographic Details
Main Authors: R Baral, G Aryal, KC Shiva Raj
Format: Article
Language:English
Published: Association of Clinical Pathologists of Nepal 2012-09-01
Series:Journal of Pathology of Nepal
Subjects:
Online Access:http://www.nepjol.info/index.php/JPN/article/view/6888
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Summary:<p><span style="font-family: Calibri;">Idiopathic Myelofibrosis is an infrequent chronic myeloproliferative disorder characterized by varying degrees of bone marrow fibrosis and extra medullary hematopoiesis, with the fibrosis being a reactive phenomenon to a neoplastic proliferation of a pluripotent hematopoietic stem cell. Idiopathic Myelofibrosis is heterogeneous in presentation and clinical course, with anemia being one of the most important problems. We present a case of a 59 year old male who presented with severe anemia, the peripheral blood picture mimicking hemolysis with numerous schistocytes and teardrop cells.</span></p><p><span style="font-family: Calibri;">Journal of Pathology of Nepal (2012) Vol. 2, 323-327</span></p><p><span style="font-family: Calibri;">DOI: <a href="http://dx.doi.org/10.3126/jpn.v2i4.6888">http://dx.doi.org/10.3126/jpn.v2i4.6888</a></span></p>
ISSN:2091-0797
2091-0908