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Table 1 Clinical characteristics of cases

From: Pathological findings with vacuoles in anti-mitochondrial antibody-positive inflammatory myopathy

 

Case 1

Case 2

Case 3

Age (y)

46

34

52

Sex

M

M

F

Duration of symptoms prior to first evaluation (mo)

5

12

36

Muscle symptoms

   

Limb weakness

UE > LE

LE > UE

LE > UE

Neck flexor

–

–

–

Muscle atrophy

–

–

–

Max CK/(U·L− 1) (reference range 25–195 U/L)

8528

806

2043

Anti-mitochondrial antibody

+

+

+

Myositis-specific antibodies

   

Associated antibodies*

ANA 1:320

Ro-52

ANA 1:1000

Ro-52

Irritable myopathy on EMG

+

+

+

Serum creatinine/(µmol·L− 1) (reference range 44–133 µmol/L)

60.11

44.46

42.00

Proteinuria

1.83 g/24 h

0.30 g/24 h

+++

Complements

   

C3/(g·L− 1) (reference range 0.6–1.5 g/L)

Not tested

1.180

0.721

C4/(g·L− 1) (reference range 0.12–0.36 g/L)

Not tested

0.064

0.168

Autoimmune diseases

   

PBC

+

+

+

AIH

–

–

+

Hashimoto thyroiditis

–

–

+

Cardiac

   

Cardiomyopathy

–

+

+

Arrhythmia

   

Heart block

+

–

+

PVC

–

+

+

AF

–

–

+

ILD

–

–

+

Respiratory failure, type 2

–

+

+

Arthritis

–

–

–

Skin rash

–

–

–

Treatments received

Pred

Pred, MTX, RTX

Pred, MTX, CTX

  1. UE, upper extremities; LE, lower extremities; CK, creatine kinase; ANA, antinuclear antibody; EMG, electromyogram; PBC, primary biliary cholangitis; AIH, autoimmune hepatitis; PVC, premature ventricular contraction; AF, atrial fibrillation; ILD, interstitial lung disease; Pred, prednisone; MTX, methotrexate; RTX, rituximab; CTX, cyclophosphamide
  2. * Other myositis-associated autoantibodies were negative unless specified here