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Created page with "{{Template:Manson}} [[Image:|centre|500px]] <br /> '''An eight-year-old crossbred dog has a history of crusting, flaky skin lesions, weight loss, lethargy and polyarthropathy..."
{{Template:Manson}}
[[Image:|centre|500px]]
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'''An eight-year-old crossbred dog has a history of crusting, flaky skin lesions, weight loss, lethargy and polyarthropathy. There is generalized, moderate lymphadenopathy. The dog was imported from Spain 18 months previously. Smears from FNAs from two lymph nodes are shown (both Giemsa, ×100 oil).'''
<br />
<FlashCard questions="4">
|q1=What cell(s) are increased in number?
|a1=
*Plasma cells (1). These cells have eccentric nuclei and a perinuclear clear area, which is the Golgi area, the site of immunoglobulin production.
*There also appear to be increased numbers of lymphoblasts (2).
|l1=Leishmania
|q2=What does this indicate?
|a2=
This indicates reactive hyperplasia and particularly plasma cell hyperplasia.
|l2=Leishmania
|q3=What is the cell next to the arrowhead?
|a3=A ‘Mott cell’. <br>
This is a plasma cell containing Russell bodies, which are accumulations of immunoglobulins within vesicles.
|l3=B cell differentiation#Plasma cells
|q4=Given the history and clinical signs, can you speculate on a possible cause for the generalized lymphadenopathy?
|a4=Plasma cell hyperplasia is caused by chronic antigenic stimulation. In this case the cause was Leishmania infection. The organisms were identified in macrophages in a bone marrow aspirate.<br><br>
Note:This case is included to emphasize recognition of basic processes and underlying mechanisms contributing to this cytological appearance. Knowledge of the significance of the finding of hyperplasia, with the history of importation from Spain, indicated that additional investigation was required to identify the suspected organism. <br><br>
Other differential diagnoses for chronic immune stimulation that could result in this appearance cytologically include
*chronic parasitic, fungal, bacterial or protozoal infections.
*Tick-borne diseases should be included in the differential in those countries or areas where tick exposure may be present.
*Sometimes, chronic, noninfectious diseases processes, including neoplasia, systemic lupus erythematosus or immune-mediated disease involving the skin and/or joints, could present with this appearance. <br><br>
Therefore, an extensive work up may be required in some cases in order to determine the most likely underlying cause. The cytological evaluation is part of this work up.
|l4=Leishmania
</FlashCard>
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[[Category:Cytology Q&A]]
[[Image:|centre|500px]]
<br />
'''An eight-year-old crossbred dog has a history of crusting, flaky skin lesions, weight loss, lethargy and polyarthropathy. There is generalized, moderate lymphadenopathy. The dog was imported from Spain 18 months previously. Smears from FNAs from two lymph nodes are shown (both Giemsa, ×100 oil).'''
<br />
<FlashCard questions="4">
|q1=What cell(s) are increased in number?
|a1=
*Plasma cells (1). These cells have eccentric nuclei and a perinuclear clear area, which is the Golgi area, the site of immunoglobulin production.
*There also appear to be increased numbers of lymphoblasts (2).
|l1=Leishmania
|q2=What does this indicate?
|a2=
This indicates reactive hyperplasia and particularly plasma cell hyperplasia.
|l2=Leishmania
|q3=What is the cell next to the arrowhead?
|a3=A ‘Mott cell’. <br>
This is a plasma cell containing Russell bodies, which are accumulations of immunoglobulins within vesicles.
|l3=B cell differentiation#Plasma cells
|q4=Given the history and clinical signs, can you speculate on a possible cause for the generalized lymphadenopathy?
|a4=Plasma cell hyperplasia is caused by chronic antigenic stimulation. In this case the cause was Leishmania infection. The organisms were identified in macrophages in a bone marrow aspirate.<br><br>
Note:This case is included to emphasize recognition of basic processes and underlying mechanisms contributing to this cytological appearance. Knowledge of the significance of the finding of hyperplasia, with the history of importation from Spain, indicated that additional investigation was required to identify the suspected organism. <br><br>
Other differential diagnoses for chronic immune stimulation that could result in this appearance cytologically include
*chronic parasitic, fungal, bacterial or protozoal infections.
*Tick-borne diseases should be included in the differential in those countries or areas where tick exposure may be present.
*Sometimes, chronic, noninfectious diseases processes, including neoplasia, systemic lupus erythematosus or immune-mediated disease involving the skin and/or joints, could present with this appearance. <br><br>
Therefore, an extensive work up may be required in some cases in order to determine the most likely underlying cause. The cytological evaluation is part of this work up.
|l4=Leishmania
</FlashCard>
{{#tag:imagemap|Image:Next Question.png{{!}}center{{!}}200px
rect 0 0 860 850 [[Cytology Q&A 09|Cytology Q&A 09]]
desc none}}
[[Category:Cytology Q&A]]