Unusual Association: Dermatomyositis Diagnosis Tied to Rare Presence of TPO Autoantibodies

The co-occurrence of autoimmune diseases is prevalent and largely documented. However, the simultaneous presence of dermatomyositis and autoimmune thyroid disorders remains comparably uncommon, despite both being autoimmune in nature. In this report, we present a case of a 60-year-old Bangladeshi American individual delineating clinical manifestations consistent with dermatomyositis, including Gottron's papules, the V-sign, Shawl sign, and skin abnormalities, noticeably hypopigmented areas on the scalp and face. Although muscle biopsy results in this patient did not align strictly with classical dermatomyositis, they illustrated a combination of necrotizing myopathy and dermatomyositis. Notably, laboratory findings conceded the presence of TPO autoantibodies, despite the absence of clinical signs or symptoms of hypothyroidism. This discovery recommends the possibility of an underlying autoimmune thyroid condition. Our case prompts consideration of whether a distinct subtype of dermatomyositis may be associated with autoimmune thyroid conditions, even in the absence of overt thyroid manifestations.

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Publication Details

Journal
Scholars Journal of Applied Medical Sciences
Published
2024-11-04
DOI
https://doi.org/10.36347/sjams.2024.v12i11.003
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
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article

Unusual Association: Dermatomyositis Diagnosis Tied to Rare Presence of TPO Autoantibodies

Dr Dipaloke Banik, Debashish Chowdhury, D. Roy
Scholars Journal of Applied Medical Sciences
Inflammatory Myopathies and Dermatomyositis
article

Unusual Association: Dermatomyositis Diagnosis Tied to Rare Presence of TPO Autoantibodies

Dr Dipaloke Banik, Debashish Chowdhury, D. Roy
article en

Abstract

The co-occurrence of autoimmune diseases is prevalent and largely documented. However, the simultaneous presence of dermatomyositis and autoimmune thyroid disorders remains comparably uncommon, despite both being autoimmune in nature. In this report, we present a case of a 60-year-old Bangladeshi American individual delineating clinical manifestations consistent with dermatomyositis, including Gottron's papules, the V-sign, Shawl sign, and skin abnormalities, noticeably hypopigmented areas on the scalp and face. Although muscle biopsy results in this patient did not align strictly with classical dermatomyositis, they illustrated a combination of necrotizing myopathy and dermatomyositis. Notably, laboratory findings conceded the presence of TPO autoantibodies, despite the absence of clinical signs or symptoms of hypothyroidism. This discovery recommends the possibility of an underlying autoimmune thyroid condition. Our case prompts consideration of whether a distinct subtype of dermatomyositis may be associated with autoimmune thyroid conditions, even in the absence of overt thyroid manifestations.

Scholars Journal of Applied Medical SciencesVol. 12(11)
Good health and well-being
Openalex Percentile: Top 70%
Inflammatory Myopathies and Dermatomyositis
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Unusual Association: Dermatomyositis Diagnosis Tied to Rare Presence of TPO Autoantibodies — Dr Dipaloke Banik, Debashish Chowdhury, et al. · Scholars Journal of Applied Medical Sciences (2024) | TGRS Research Map | TGRS