Evidence map›Paper›PMID 39814065›Full record

ArticleThe Journal of small animal practice2025

Acute and chronic systemic inflammation associated with canine nodular splenic lesions composed of heterogeneous cell components: four cases (2020-2024).

K Mourou, Y Abou Monsef, S Belluco, M Penent, M Delverdier, M Hugonnard, F Granat, R Lavoue, M Mantelli

Abstract readCase Reports
In one paragraph

Article in The Journal of small animal practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

K MourouService de Médecine Interne, Département des Animaux de Compagnie de Loisir et de Sport, Université de Lyon, VetAgro Sup, Campus Vétérinaire de Lyon, Marcy-l'Étoile, France.ORCID 0009-0001-1815-3836
Y Abou MonsefLaboratoire d'Histopathologie Vétérinaire, Université de Toulouse, École Nationale Vétérinaire de Toulouse, Toulouse Cedex, France.
S BellucoLaboratoire d'Histopathologie Vétérinaire, VetAgro Sup, Campus Vétérinaire, Marcy l'étoile, France.
M PenentLaboratoire d'Histopathologie Vétérinaire, Université de Toulouse, École Nationale Vétérinaire de Toulouse, Toulouse Cedex, France.
M DelverdierLaboratoire d'Histopathologie Vétérinaire, Université de Toulouse, École Nationale Vétérinaire de Toulouse, Toulouse Cedex, France.
M HugonnardService de Médecine Interne, Département des Animaux de Compagnie de Loisir et de Sport, Université de Lyon, VetAgro Sup, Campus Vétérinaire de Lyon, Marcy-l'Étoile, France.
F GranatLaboratoire Central de Biologie Médicale, ENVT, Toulouse, France.
R LavoueUniversité de Toulouse, Toulouse, France.
M MantelliUniversité de Toulouse, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo describe the clinical presentation and clinicopathological findings of dogs with nodular splenic lesions composed of heterogeneous cell components associated with systemic inflammation and to provide information on the outcome after surgical resection. MATERIALS AND

methodsMedical records were searched for dogs with histologically and immunohistochemically characterised nodular splenic lesions with mixed stromal, histiocytic and lymphoid cells and the presence of systemic inflammatory markers at the time of diagnosis.

resultsFour dogs were included, of which three had an undifferentiated splenic stromal sarcoma and one had a splenic leiomyosarcoma. Fever and abdominal pain were reported in three and four cases, respectively. All dogs showed hyperglobulinaemia and marked changes in the serum protein electrophoresis profile. C-reactive protein and fibrinogen concentrations were both increased in three cases. These abnormalities completely resolved after splenectomy. Moreover, two dogs had concomitant glomerular disease and one dog had liver amyloidosis. Three dogs were still alive and asymptomatic 1, 6 and 9 months after surgery. One dog died 16 months after the initial presentation due to complications related to progressive renal failure. CLINICAL SIGNIFICANCE: Based on this report, nodular splenic lesions with heterogeneous cell components may directly be associated with a pro-inflammatory state and should be considered as part of the differential diagnosis of fever and hyperglobulinaemia in dogs. Furthermore, early recognition and treatment of these lesions could reduce the risk of systemic complications potentially associated with amyloid deposit and organ failure.

Indexed as

Dog DiseasesInflammationSplenic DiseasesSplenic NeoplasmsAnimalsChronic DiseaseDogsFemaleMaleSpleenSplenectomy

Identifiers

PMID39814065
PMCPMC12000714

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