TABLE 65-3.
Morphological and Functional Disorders of Canine and Feline Leukocytes
| DISORDER | INHERITANCE | CAUSE | SPECIES | APPEARANCE/CLINICAL SIGNS | DIAGNOSIS | TREATMENT | REFERENCES |
|---|---|---|---|---|---|---|---|
| Cyclic hematopoiesis | Autosomal recessive | Stem cell abnormality | Gray-coated collie, collie- mix dogs |
|
|
|
Campbell (1985), Lothrop et al. (1988), Niemeyer and Lothrop (2000) |
| Inherited vitamin B12 (cobalamin) malabsorption | Autosomal recessive | Failure to express intestinal intrinsic factor cobalamin complex receptor (cubilin) | Inbred giant schnauzer | Nuclear chromatin maturation abnormalities, neutropenia, nonregenerative anemia |
|
|
Fyfe (2000) |
| Birman cat neutrophil granulation anomaly | Autosomal recessive | Fine azurophilic granules similar to progranulocyte granules | Birman cat | Prominent neutrophil granulation |
|
None; neutrophils function normally | Hirsch and Cunningham (1984) |
| Canine leukocyte adhesion deficiency | Autosomal recessive | Deficient expression of CD18 (subunit of B2 integrins) | Irish setter |
|
Flow cytometry for neutrophil CD18 expression |
|
Andreason and Roth (2000) |
| Pelger-Huët anomaly |
|
Failure of the mature nucleus to form true filaments | Cats, dogs | Peanut-shaped nuclei in granulocytes, monocytes, or megakaryocytes | Serial CBCs | None; neutrophils function normally | |
| Chédiak-Higashi syndrome | Autosomal recessive | Failure of granule fusion | Persian cats |
|
|
|
Meyers (2000) |
CBC, Complete blood count; rhG-CSF, recombinant human granulocyte-colony stimulating factor; IM, intramuscularly; MPS, mucopolysaccharidosis; MPD, myeloproliferative disease.