36º Congresso Brasileiro de Reumatologia

Página Inicial » Inscrições Científicas » Trabalhos

Dados do Trabalho


Title

LATE-ONSET POMPE DISEASE MIMICKING ADULT POLYMYOSITIS: A CASE REPORT

Background

Pompe disease is a metabolic myopathy characterized by lysosomal acid alpha-glycosidase deficiency. The disease is uncommon in the adult population and may be confused with other myopathies, including polymyositis.

Case report

A 44 year old female patient. She started a progressive, symmetrical, and predominantly proximal muscle weakness of the limbs at 33 years old. At that time, the patient had a serum creatine phosphokinase level of 8000U/L, muscle biopsy compatible with inflammatory myopathy and electroneuromyography with myopathic pattern. With a polymyositis hypothesis, the patient received pulse therapy with methylprednisolone 3g, intravenous immunoglobulin and several immunosuppressants (methotrexate, azathioprine, cyclosporine) and rituximab (2g, 4 complete cycles). After 11 years, the patient has maintained a relatively stable clinical picture, with CPK of 576U/L, but with permanent muscular weakness, especially of the lower limbs. Therefore, magnetic resonance imaging of the thighs was performed 9 years later, showing presence of diffuse liposubstitution and atrophy, predominating in the minimal and medium gluteal muscles, piriformis, hamstring muscles and adductor muscle group. No report of involvement of other organs and systems. The patient was submitted to a new muscular biopsy that showed presence of dystrophic pattern, with intracytoplasmic vacuoles, absence of inflammatory infiltrate and increased acid phosphatase activity in the vacuoles. As a complementary examination, a significant reduction in serum alpha-glycosidic acid levels was observed, as well as the existence of two mutations in the two alleles of the acid alpha-glycosidase gene, defining the diagnosis of Pompe disease.

Conclusion

Pompe's disease consists of a rare metabolic myopathy that remains as a challenging differential diagnosis within the polymyositis-like condition, being relevant its report in the clinical context of neuromuscular disease.

Área

Muscular Diseases

Autores

Bruna Kellen Wanderley Porto, Carla Baleeiro Rodrigues Silva, Rodrigo Silveira Vasconcelos, Luma Mendes Brito, Marlise Sitima Mendes Simões Faria, Samuel Katsuyuki Shinjo