| histiocytic medullary reticulosis |
A form of malignant histiocytosis marked by anemia; granulocytopenia; enlargement of the spleen, liver, and lymph nodes; and phagocytosis of red blood cells.
Ãâó:
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| histiocytic l. |
acute monocytic l.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| histiocytic medullary r. |
a fatal hereditary disorder transmitted as an autosomal recessive trait, characterized by anemia, granulocytopenia, thrombocytopenia, intense phagocytosis of red blood cells, diffuse proliferation of histiocytes of various organs, and enlargement of the liver, spleen, and lymph nodes. Called also familial hemophagocytic r., familial histiocytic r., and Omenn's syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| histiocytic necrotizing l. |
Kikuchi's l.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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