1. Adult-type dermatomyositis with secondary lymphoid follicles harbouring reactive B-cells component
- Author
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Yazid Maghrabi, Sahar Hakamy, Ahmad R. Abuzinadah, Maher Kurdi, Nizar Bahabri, and Mohammed AlSobaei
- Subjects
Pathology ,medicine.medical_specialty ,Proximal muscle weakness ,Muscle biopsy ,medicine.diagnostic_test ,business.industry ,Muscle weakness ,Skeletal muscle ,Dermatomyositis ,medicine.disease ,Rash ,Lymphocytic Infiltrate ,Inflammatory myopathy ,medicine.anatomical_structure ,Neurology ,Pediatrics, Perinatology and Child Health ,medicine ,Neurology (clinical) ,medicine.symptom ,business ,Genetics (clinical) - Abstract
Dermatomyositis (DM) is an immune-mediated inflammatory disease characterized by pathognomic lesions in skin and skeletal muscle including lymphocytic infiltrates. It rarely presents with ectopic lymphoid structures, as other autoimmune and chronic inflammatory diseases. We describe a case of a 47-year-old male, who presented clinically with proximal muscle weakness, skin rash and elevated creatin kinase (CK) levels. The muscle biopsy revealed inflammatory myopathy, with perifascicular pathology, and scattered ectopic lymphoid follicles-like structures harboring reactive B-cells. Clonality analysis of B-cells using polymerase chain reaction ruled out malignant lymphoma. The patient responded favorably to steroid therapy, and his muscle weakness improved. In conclusion, the clinical and histopathologic features of DM can be atypical, and the presence of lymphoid follicles, although rare, is not inevitably linked to an unfavorable prognosis.
- Published
- 2021
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