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Table 4 Histological changes in the 32 Hungarian Vizslas with biopsy-confirmed polymyopathy

From: Clinical features of idiopathic inflammatory polymyopathy in the Hungarian Vizsla

Histopathological changes (Total 32)

Group 1

Group 2

25 total dogs (biopsies) (confirmed VIP diagnosis)

7 dogs (3 biopsies, 1 biopsy and post-mortem/3 post-mortem) (myopathy diagnosis)

Inflammatory change e.g. Lymphohistiocytic inflammation

Variability in myofibres size with multifocal endomysial, interstitial and perivascular mononuclear cell infiltrations (lymphocytes & macrophages +/− plasma cells, eosinophils) of non-necrotic fibres. Underlying inflammatory process masked by corticosteroid treatment in one case.

 

25 dogs

0 dogs

Myopathic change

 

Variation in the myofibre size without inflammatory infiltration.

0 dogs

7 dogs

Adipose tissue

Small amount of adipose tissue associated with fibrosis.

Adipocytes present in some fascicles (endomysium and perimysium).

2 dogs

1 dogs

Fibrosis

None OR perimisial/endomysial fibrosis OR occasionally area of fibrosis with lack of myofibres with any significant inflammation (primary or secondary?)

 

3 dogs

0 dogs

Degenerative changes

Either any appreciable myofibre degeneration or active degenerative changes within the muscle fibres (variation in myofibre diameter, atrophy with round to polygonal/angular shape, hyalinisation, nuclear internalisation, sarcolemmal fragmentation).

Variation in muscle fibres, atrophy (occasionally smaller fibres grouped together, some angular but most round to polygonal profile), nuclear internalisation.

19 dogs

4 dogs

Regenerative changes

Nuclear rowing, centralisation/hyperthrophy of the nuclei increased cytoplasmic basophilia, type 2 fibres.

Occasional enlarged and round myofibres (compensatory hypertrophy), and nuclear rowing.

13 dogs

3 dogs

Necrotic fibres

Scattered to severe necrotic myofibres with some undergoing phagocytosis.

 

7 dogs

0 dogs

Fibrosis

Mild to moderate endomysial and perimysial fibrosis secondary to myofibre loss.

Increased endomysial and perimysial connective tissue secondary to myofibre loss.

7 dogs

2 dogs

Intramuscular nerve branches

Normal (25 dogs)

Normal (7 dogs)

Immunoreagent SPA-HRPO

Present in two cases

 

(Antibodies against endplate proteins)

Dystrophin protein

 

Decreased staining for carboxy terminus of the dystrophin protein was found in one case; however, the dog improved on immunosuppressive treatment and the suspicion for muscle dystrophy was abandoned.