Clinical case and features of progression of dermatomyositis with anti-Mi2 antibodies

Aim. To present a clinical case and describe the features of dermatomyositis (DM) with myositis-specific anti-Mi2 antibodies (MSAs).Material and methods. Clinical manifestations, abnormalities of laboratory and immunologic tests, strategy and efficacy of pharmacotherapy in a patient with DM are desc...

Full description

Saved in:
Bibliographic Details
Main Authors: I. V. Devald, E. A. Khodus, M. S. Belsner, O. L. Minakina, D. S. Stashkevich
Format: Article
Language:Russian
Published: ABV-press 2025-07-01
Series:Klinicist
Subjects:
Online Access:https://klinitsist.abvpress.ru/Klin/article/view/650
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849396748684886016
author I. V. Devald
E. A. Khodus
M. S. Belsner
O. L. Minakina
D. S. Stashkevich
author_facet I. V. Devald
E. A. Khodus
M. S. Belsner
O. L. Minakina
D. S. Stashkevich
author_sort I. V. Devald
collection DOAJ
description Aim. To present a clinical case and describe the features of dermatomyositis (DM) with myositis-specific anti-Mi2 antibodies (MSAs).Material and methods. Clinical manifestations, abnormalities of laboratory and immunologic tests, strategy and efficacy of pharmacotherapy in a patient with DM are described.Results. A clinical case of DM is presented in a patient born in 1992. The disease manifested through lesions in the skin (periorbital edema with heliotropic rash, Gottron papules, diffuse alopecia, cheilitis, digital ulcers), mucous membranes (enanthem), muscles (myalgia), joints (polyarthritis), peripheral nervous system (polyneuropathy), and constitutional symptoms (weight loss, general weakness, subfebrile temperature). Laboratory examination showed increased erythrocyte sedimentation rate of 40 mm/h and lactate dehydrogenase level of 672 U/L, antinuclear factor was measured at 1:320, and anti-Mi2 antibodies were detected by MSAs panel. Combination immunosuppressive therapy with methylprednisolone at an initial dose of 1 mg/kg/day and subcutaneous methotrexate at a dose of 15 mg/week was initiated, followed by correction depending on the clinical and laboratory dynamics. This case demonstrates benign course of anti-Mi2 antibody-positive DM. Classic skin symptoms (periorbital edema with heliotrope rash, Gottron papules) and muscle damage completely regressed after 21 months of combination pharmacotherapy with methylprednisolone and methotrexate. Stable immunological seroconversion of MSAs and drug-free clinical remission were achieved. Low risk of malignant neoplasms with this DM serotype is emphasized. Atypical symptoms of polyneuropathy and myalgia are considered.Conclusion. The presented clinical case demonstrates the characteristic features of the DM subtype with anti-Mi2 antibodies: a combination of classic skin symptoms with muscle damage, benign course during two-year combination pharmacotherapy with a glucocorticoid and a cytostatic, persistent immunological seroconversion of MSAs, drug-free clinical remission. Presumably, determination of DM serotype can be useful in clinical practice for predicting the course of the disease, response to pharmacotherapy, and the risk of developing neoplasia.
format Article
id doaj-art-df593e00a7c6457f878edf5c93824921
institution Kabale University
issn 1818-8338
language Russian
publishDate 2025-07-01
publisher ABV-press
record_format Article
series Klinicist
spelling doaj-art-df593e00a7c6457f878edf5c938249212025-08-20T03:39:14ZrusABV-pressKlinicist1818-83382025-07-01191475310.17650/1818-8338-2025-19-1-K733459Clinical case and features of progression of dermatomyositis with anti-Mi2 antibodiesI. V. Devald0E. A. Khodus1M. S. Belsner2O. L. Minakina3D. S. Stashkevich4South Ural State Medical University; Chelyabinsk State Universit; Clinic of Professor KinzerskyChelyabinsk State Universit; Clinic of Professor KinzerskySouth Ural State Medical UniversitySouth Ural State Medical UniversityChelyabinsk State UniversitAim. To present a clinical case and describe the features of dermatomyositis (DM) with myositis-specific anti-Mi2 antibodies (MSAs).Material and methods. Clinical manifestations, abnormalities of laboratory and immunologic tests, strategy and efficacy of pharmacotherapy in a patient with DM are described.Results. A clinical case of DM is presented in a patient born in 1992. The disease manifested through lesions in the skin (periorbital edema with heliotropic rash, Gottron papules, diffuse alopecia, cheilitis, digital ulcers), mucous membranes (enanthem), muscles (myalgia), joints (polyarthritis), peripheral nervous system (polyneuropathy), and constitutional symptoms (weight loss, general weakness, subfebrile temperature). Laboratory examination showed increased erythrocyte sedimentation rate of 40 mm/h and lactate dehydrogenase level of 672 U/L, antinuclear factor was measured at 1:320, and anti-Mi2 antibodies were detected by MSAs panel. Combination immunosuppressive therapy with methylprednisolone at an initial dose of 1 mg/kg/day and subcutaneous methotrexate at a dose of 15 mg/week was initiated, followed by correction depending on the clinical and laboratory dynamics. This case demonstrates benign course of anti-Mi2 antibody-positive DM. Classic skin symptoms (periorbital edema with heliotrope rash, Gottron papules) and muscle damage completely regressed after 21 months of combination pharmacotherapy with methylprednisolone and methotrexate. Stable immunological seroconversion of MSAs and drug-free clinical remission were achieved. Low risk of malignant neoplasms with this DM serotype is emphasized. Atypical symptoms of polyneuropathy and myalgia are considered.Conclusion. The presented clinical case demonstrates the characteristic features of the DM subtype with anti-Mi2 antibodies: a combination of classic skin symptoms with muscle damage, benign course during two-year combination pharmacotherapy with a glucocorticoid and a cytostatic, persistent immunological seroconversion of MSAs, drug-free clinical remission. Presumably, determination of DM serotype can be useful in clinical practice for predicting the course of the disease, response to pharmacotherapy, and the risk of developing neoplasia.https://klinitsist.abvpress.ru/Klin/article/view/650dermatomyositismyositis-specific antibodiesanti-mi2 antibodiesmethotrexatemethylprednisoloneseroconversiondrug-free remissionprognosis
spellingShingle I. V. Devald
E. A. Khodus
M. S. Belsner
O. L. Minakina
D. S. Stashkevich
Clinical case and features of progression of dermatomyositis with anti-Mi2 antibodies
Klinicist
dermatomyositis
myositis-specific antibodies
anti-mi2 antibodies
methotrexate
methylprednisolone
seroconversion
drug-free remission
prognosis
title Clinical case and features of progression of dermatomyositis with anti-Mi2 antibodies
title_full Clinical case and features of progression of dermatomyositis with anti-Mi2 antibodies
title_fullStr Clinical case and features of progression of dermatomyositis with anti-Mi2 antibodies
title_full_unstemmed Clinical case and features of progression of dermatomyositis with anti-Mi2 antibodies
title_short Clinical case and features of progression of dermatomyositis with anti-Mi2 antibodies
title_sort clinical case and features of progression of dermatomyositis with anti mi2 antibodies
topic dermatomyositis
myositis-specific antibodies
anti-mi2 antibodies
methotrexate
methylprednisolone
seroconversion
drug-free remission
prognosis
url https://klinitsist.abvpress.ru/Klin/article/view/650
work_keys_str_mv AT ivdevald clinicalcaseandfeaturesofprogressionofdermatomyositiswithantimi2antibodies
AT eakhodus clinicalcaseandfeaturesofprogressionofdermatomyositiswithantimi2antibodies
AT msbelsner clinicalcaseandfeaturesofprogressionofdermatomyositiswithantimi2antibodies
AT olminakina clinicalcaseandfeaturesofprogressionofdermatomyositiswithantimi2antibodies
AT dsstashkevich clinicalcaseandfeaturesofprogressionofdermatomyositiswithantimi2antibodies