2014
DOI: 10.1186/preaccept-1335140742127765
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Evaluation of blood and bone marrow in selected canine vector-borne diseases

Abstract: Background: Bone marrow (BM) is a major hematopoietic organ that can harbour a variety of vector-borne pathogens; however, knowledge of BM pathological changes in dogs infected with vector-borne pathogens is limited. Thus, the aim of the present study was to assess the pathological changes in canine BM associated with natural infections by four vector-borne pathogens, as well as to determine the relationships between such changes and abnormalities of the peripheral blood.

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Cited by 16 publications
(24 citation statements)
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“…The underlying bone marrow pathology in leishmaniasis‐associated pancytopoenia has yet to be fully elucidated. In previous studies in dogs with leishmaniasis and various blood mono‐ or bicytopoenias, bone marrow changes included myeloid hyperplasia, erythroid hypoplasia, erythrophagocytosis, mild‐to‐moderate dysplastic changes affecting all three haematopoietic lineages, megakaryocytic emperipolesis, lymphocytosis and plasmacytosis, but generalised bone marrow aplasia was not documented (Foglia Manzillo et al , Nicolato et al , De Tommasi et al ). In the present study, 8 of 10 dogs with leishmaniasis subject to bone marrow cytology examination were normocellular, one demonstrated severe megakaryocytic aplasia and a single dog had severe aplasia of all three lineages.…”
Section: Discussionmentioning
confidence: 98%
See 1 more Smart Citation
“…The underlying bone marrow pathology in leishmaniasis‐associated pancytopoenia has yet to be fully elucidated. In previous studies in dogs with leishmaniasis and various blood mono‐ or bicytopoenias, bone marrow changes included myeloid hyperplasia, erythroid hypoplasia, erythrophagocytosis, mild‐to‐moderate dysplastic changes affecting all three haematopoietic lineages, megakaryocytic emperipolesis, lymphocytosis and plasmacytosis, but generalised bone marrow aplasia was not documented (Foglia Manzillo et al , Nicolato et al , De Tommasi et al ). In the present study, 8 of 10 dogs with leishmaniasis subject to bone marrow cytology examination were normocellular, one demonstrated severe megakaryocytic aplasia and a single dog had severe aplasia of all three lineages.…”
Section: Discussionmentioning
confidence: 98%
“…Pancytopoenia has been inconsistently reported in leishmaniasis, with 0 to 12% of the affected dogs being pancytopoenic on admission (Mylonakis et al , Petanides et al , De Tommasi et al ). Evidence provided in this study suggests that, in endemic areas, leishmaniasis may account for 23·5 and 33·6% of pancytopoenic dogs, when considered singly or in co‐occurrence with monocytic ehrlichiosis, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…Its importance increases as regards the diagnosis of endemic infectious diseases, as in the present study location: canine monocytic ehrlichiosis (CME) and canine visceral leishmaniasis (CVL) (SILVA et al, 2010;ALMEIDA et al, 2012). A variety of medullary responses to caused stress by various infections and parasitism have been related (DE TOMMASI et al, 2014).…”
Section: Introductionmentioning
confidence: 79%
“…These features included splenomegaly, EMH, anemia, leukopenia, RBC anisocytosis and poikilocytosis, and hypercellularity, moderate fibrosis and clustering of atypical megakaryocytes, indicating abnormal megakaryopoiesis, in bone marrow. It should be noted that certain disorders, such as immune‐mediated hemolytic anemia and/or immune‐mediated thrombocytopaenia, lymphoma, drug toxicities, and infectious diseases have been associated with both secondary myelofibrosis and megakaryocytic dysplasia . Considering the lack of molecular testing for an extensive panel of infectious diseases as well as a Coomb's test (due financial constraints), secondary myelofibrosis potentially due to a nonregenerative immune‐mediated or infectious etiology could not be definitively excluded in this dog .…”
Section: Discussionmentioning
confidence: 96%