Total: 103 |
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PMID (PMCID) | ||
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31153385 |
OTHER | |
Paraneoplastic dermatomyositis appearing after nivolumab therapy for gastric cancer: a case report. | ||
Shibata C, Kato J, Toda N, Imai M, Fukumura Y, Arai J, Kurokawa K, Kondo M, Takagi K, Kojima K, Ohki T, Seki M, Yoshida M, Suzuki A, Tagawa K. J Med Case Rep. 2019;13(1):168. |
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We experienced such a case in which we had difficulties in diagnosing paraneoplastic dermatomyositis or drug-associated myositis. | ||
31153385 |
OTHER | |
Paraneoplastic dermatomyositis appearing after nivolumab therapy for gastric cancer: a case report. | ||
Shibata C, Kato J, Toda N, Imai M, Fukumura Y, Arai J, Kurokawa K, Kondo M, Takagi K, Kojima K, Ohki T, Seki M, Yoshida M, Suzuki A, Tagawa K. J Med Case Rep. 2019;13(1):168. |
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While dermatomyositis is often associated with malignancy, several autoimmune diseases like myositis can be caused by immune checkpoint inhibitors. | ||
31153385 |
OTHER | |
Paraneoplastic dermatomyositis appearing after nivolumab therapy for gastric cancer: a case report. | ||
Shibata C, Kato J, Toda N, Imai M, Fukumura Y, Arai J, Kurokawa K, Kondo M, Takagi K, Kojima K, Ohki T, Seki M, Yoshida M, Suzuki A, Tagawa K. J Med Case Rep. 2019;13(1):168. |
||
Differentially diagnosing paraneoplastic dermatomyositis or drug-associated myositis caused by immune checkpoint inhibitors is difficult in some cases. | ||
31153385 |
OTHER | |
Paraneoplastic dermatomyositis appearing after nivolumab therapy for gastric cancer: a case report. | ||
Shibata C, Kato J, Toda N, Imai M, Fukumura Y, Arai J, Kurokawa K, Kondo M, Takagi K, Kojima K, Ohki T, Seki M, Yoshida M, Suzuki A, Tagawa K. J Med Case Rep. 2019;13(1):168. |
||
Differentially diagnosing malignancy-associated dermatomyositis or myositis caused by immune checkpoint inhibitors is sometimes difficult, particularly when a patient with malignancy shows the symptoms of myositis after checkpoint inhibitor administration. | ||
31153385 |
OTHER | |
Paraneoplastic dermatomyositis appearing after nivolumab therapy for gastric cancer: a case report. | ||
Shibata C, Kato J, Toda N, Imai M, Fukumura Y, Arai J, Kurokawa K, Kondo M, Takagi K, Kojima K, Ohki T, Seki M, Yoshida M, Suzuki A, Tagawa K. J Med Case Rep. 2019;13(1):168. |
||
Differentially diagnosing malignancy-associated dermatomyositis or myositis caused by immune checkpoint inhibitors is sometimes difficult, particularly when a patient with malignancy shows the symptoms of myositis after checkpoint inhibitor administration. | ||
29287518 |
MALE | Middle Aged |
Anti-MDA5 positive dermatomyositis complicated with rapidly progressive interstitial lung disease - a case report. | ||
De Backer E, Gremonprez F, Brusselle G, Depuydt P, Van Dorpe J, Van Haverbeke C, Goeminne PC, Derom E. Acta Clin Belg. 2018;73(6):413-417. |
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Myositis specific antibodies (MSA) can be used for diagnosis and predicting prognosis in patients with polymyositis and dermatomyositis. | ||
30042104 |
FEMALE | Adult |
Double-positive with positive anti-glomerular basement membrane antibody and ANCA-positive disease in a patient with dermatomyositis. | ||
Dein EJ, Crespo-Bosque M, Timlin H, Geetha D. BMJ Case Rep. 2018;2018:. |
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Approximately one in four patients (23.3%) with inflammatory myositis including dermatomyositis can require evaluation for acute kidney injury. | ||
29571300 (5866516) |
FEMALE | Middle Aged |
Erythroderma and extensive poikiloderma - a rare initial presentation of dermatomyositis: a case report. | ||
Herath HMMTB, Keragala BSDP, Pahalagamage SP, Janappriya GHCC, Kulatunga A, Gunasekera CN. J Med Case Rep. 2018;12(1):83. |
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Electromyography and muscle biopsy were supportive of inflammatory myositis and skin biopsy showed evidence of dermatomyositis. | ||
30583602 |
OTHER | |
Heart⁻Lung⁻Muscle Anti-SAE Syndrome: An Atypical Severe Combination. | ||
Zamora E, Seder-Colomina E, Holgado S, Quirant-Sanchez B, Mate JL, Martinez-Caceres EM, Casafont I, Bayes-Genis A. J Clin Med. 2018;8(1):. |
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A comprehensive immune work-up revealed anti-small ubiquitin-like modifier-1 activating enzyme (anti-SAE) antibody, a novel myositis-specific antibody, previously described mainly with overt cutaneous dermatomyositis and late skeletal muscle manifestations. | ||
30632536 |
OTHER | |
Histological Findings of Organizing Pneumonia, Based on Transbronchial Lung Biopsy, May Predict Poor Outcome in Polymyositis and Dermatomyositis: Report of Two Autopsied Cases. | ||
Oiwa H, Kondo T, Funaki M, Morito T, Yasui H, Kamiya T. Arch Rheumatol. 2018;33(3):376-380. |
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Our experience indicates that transbronchial biopsy findings of organizing pneumonia may be a poor prognostic factor in clinically amyopathic dermatomyositis and polymyositis, in spite of the profile of myositis-specific antibodies. | ||
29464127 (5804115) |
OTHER | |
Use of High-Flow Nasal Cannula Oxygen Therapy in a Pregnant Woman with Dermatomyositis-Related Interstitial Pneumonia. | ||
Shoji T, Umegaki T, Nishimoto K, Anada N, Ando A, Uba T, Kusunoki M, Oku K, Kamibayashi T. Case Rep Crit Care. 2017;2017:4527597. |
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The patient's condition improved after 7 days of hospitalization; by this time, she was positive for myositis-specific autoantibodies and was diagnosed with interstitial pneumonia preceding dermatomyositis. | ||
28668260 |
FEMALE | |
[Amyopathic dermatomyositis (DM) with anti-MDA5 antibodies, associated with bullous pemphigoid, Sjogren syndrome and gastric MALT lymphoma]. | ||
Garcia B, Dabouz F, Pascal L, Gillard M, Modiano P. Ann Dermatol Venereol. 2017;144(10):629-633. |
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The inflammatory myopathies are a heterogeneous group of muscle diseases and comprise polymyositis, dermatomyositis (DM), myopathies associated with cancers, necrotising myositis and inclusion body myositis. | ||
26759443 |
FEMALE | Middle Aged |
Colonic vasculopathy and perforation in the initial presentation of adult dermatomyositis in a patient with improving muscle weakness. | ||
Kibbi N, Bekui A, Buckley LM. BMJ Case Rep. 2016;2016:. |
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Muscle biopsy confirmed myositis, and serological studies were consistent with dermatomyositis (DM), without evidence of overlapping connective tissue disease or malignancy. | ||
24638953 (4145214) |
MALE | Middle Aged |
Dermatomyositis as a complication of interferon-alpha therapy: a case report and review of the literature. | ||
Shiba H, Takeuchi T, Isoda K, Kokunai Y, Wada Y, Makino S, Hanafusa T. Rheumatol Int. 2014;34(9):1319-22. |
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We made a diagnosis of dermatomyositis according to these clinical features, proximal muscle-predominant myogenic change on electromyography, and infiltration of monocytes and CD4+-dominant lymphocytes on skin biopsy, although myositis-associated antibodies were absent. | ||
25347903 |
FEMALE | Adult |
[Inflammatory myopathy with initial respiratory muscles involvement and rheumatoid arthritis]. | ||
Hunter M, Telias I, Collado V, Sarano J, Alvarez C, Suarez JP. Medicina (B Aires). 2014;74(5):393-6. |
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The most common inflammatory myopathies seen in practice can be separated into four distinct subsets: polymyositis, dermatomyositis, necrotizing autoimmune myositis and inclusion body myositis. | ||
23423441 |
MALE | Middle Aged |
Antisynthetase antibody syndrome: case report and review of the literature. | ||
Uribe L, Ronderos DM, Diaz MC, Gutierrez JM, Mallarino C, Fernandez-Avila DG. Clin Rheumatol. 2013;32(5):715-9. |
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This diagnosis should always come to mind in patients that present with signs of myositis, dermatomyositis, or polymyositis associated with interstitial lung disease. | ||
22618987 |
FEMALE | Middle Aged |
Living-donor lobar lung transplantation for rapidly progressive interstitial pneumonia associated with clinically amyopathic dermatomyositis: report of a case. | ||
Shoji T, Bando T, Fujinaga T, Chen F, Sasano H, Yukawa N, Mimori T, Date H. Gen Thorac Cardiovasc Surg. 2013;61(1):32-4. |
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The manifestations of collagen disease are variable and dermatomyositis (DM) is often considered a contraindication for lung transplantation because of active myositis and a high incidence of malignancy. | ||
22515579 |
FEMALE | |
Hydroxyurea-induced dermatomyositis: true amyopathic dermatomyositis or dermatomyositis-like eruption? | ||
Nofal A, El-Din ES. Int J Dermatol. 2012;51(5):535-41. |
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Hydroxyurea-induced dermatomyositis is a rare drug-induced dermatomyositis characterized by skin lesions identical to classic dermatomyositis without clinical or laboratory evidence of myositis. | ||
22515579 |
FEMALE | |
Hydroxyurea-induced dermatomyositis: true amyopathic dermatomyositis or dermatomyositis-like eruption? | ||
Nofal A, El-Din ES. Int J Dermatol. 2012;51(5):535-41. |
||
Hydroxyurea-induced dermatomyositis is a rare drug-induced dermatomyositis characterized by skin lesions identical to classic dermatomyositis without clinical or laboratory evidence of myositis. | ||
22515579 |
FEMALE | |
Hydroxyurea-induced dermatomyositis: true amyopathic dermatomyositis or dermatomyositis-like eruption? | ||
Nofal A, El-Din ES. Int J Dermatol. 2012;51(5):535-41. |
||
Hydroxyurea-induced dermatomyositis is a rare drug-induced dermatomyositis characterized by skin lesions identical to classic dermatomyositis without clinical or laboratory evidence of myositis. |