Dermatomyositis

A type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness.

Lung adenocarcinoma



Total: 13

                      


(per page)
PMID (PMCID)
30766682
OTHER
Lung adenocarcinoma and anti-transcriptional intermediary factor 1-gamma positive dermatomyositis complicated with spontaneous oesophageal rupture.
Saraya T, Tamura M, Kasuga K, Fujiwara M, Takizawa H.
Respirol Case Rep. 2019;7(3):e00403.
Lung adenocarcinoma and anti-transcriptional intermediary factor 1-gamma positive dermatomyositis complicated with spontaneous oesophageal rupture.
29526968
(6120830)
MALE Adult
Advanced Lung Adenocarcinoma with Nivolumab-associated Dermatomyositis.
Kudo F, Watanabe Y, Iwai Y, Miwa C, Nagai Y, Ota H, Yabe H, Demitsu T, Hagiwara K, Koyama N, Koyama S.
Intern Med. 2018;57(15):2217-2221.
Advanced Lung Adenocarcinoma with Nivolumab-associated Dermatomyositis.
29151514
(5891532)
FEMALE Middle Aged
Dermatomyositis Complicated by Digital Ischemia and Lung Adenocarcinoma in a Patient with Positive Anti-signal Recognition Particle Antibodies.
Nawata T, Kubo M, Mitsui H, Oishi K, Omoto M, Kanda T, Yano M.
Intern Med. 2018;57(6):883-886.
A 58-year-old Japanese woman was diagnosed with anti-signal recognition particle (SRP)-positive dermatomyositis associated with Sjogren's syndrome, rheumatoid arthritis and lung adenocarcinoma.
29151514
(5891532)
FEMALE Middle Aged
Dermatomyositis Complicated by Digital Ischemia and Lung Adenocarcinoma in a Patient with Positive Anti-signal Recognition Particle Antibodies.
Nawata T, Kubo M, Mitsui H, Oishi K, Omoto M, Kanda T, Yano M.
Intern Med. 2018;57(6):883-886.
Dermatomyositis Complicated by Digital Ischemia and Lung Adenocarcinoma in a Patient with Positive Anti-signal Recognition Particle Antibodies.
29415746
(5804049)
FEMALE
Ground-glass opacity heralding invasive lung adenocarcinoma with prodromal dermatomyositis: a case report.
Beel AJ, Demos DS, Chung A, Liao C, Lui NS.
J Cardiothorac Surg. 2018;13(1):20.
We report the case of a 72-year-old female patient with dermatomyositis - treated with a combination of prednisone, methotrexate, and intravenous immunoglobulin - and an indolent, subsolid, non-hypermetabolic pulmonary lesion, which was determined to be invasive primary lung adenocarcinoma.
29415746
(5804049)
FEMALE
Ground-glass opacity heralding invasive lung adenocarcinoma with prodromal dermatomyositis: a case report.
Beel AJ, Demos DS, Chung A, Liao C, Lui NS.
J Cardiothorac Surg. 2018;13(1):20.
While dermatomyositis prodromal to lung adenocarcinoma is not without precedent, association with an indolent, subsolid lesion has, to the best of our knowledge, not been reported.
29415746
(5804049)
FEMALE
Ground-glass opacity heralding invasive lung adenocarcinoma with prodromal dermatomyositis: a case report.
Beel AJ, Demos DS, Chung A, Liao C, Lui NS.
J Cardiothorac Surg. 2018;13(1):20.
Ground-glass opacity heralding invasive lung adenocarcinoma with prodromal dermatomyositis: a case report.
26851947
(4744381)
FEMALE Adult
A mild form of dermatomyositis as a prodromal sign of lung adenocarcinoma: a case report.
Papakonstantinou E, Kapp A, Raap U.
J Med Case Rep. 2016;10:34.
She was diagnosed with paraneoplastic dermatomyositis as the first sign of a lung adenocarcinoma.
26851947
(4744381)
FEMALE Adult
A mild form of dermatomyositis as a prodromal sign of lung adenocarcinoma: a case report.
Papakonstantinou E, Kapp A, Raap U.
J Med Case Rep. 2016;10:34.
Here we report a case of a woman with dermatomyositis who was diagnosed with lung adenocarcinoma in the setting of weight loss, progressive fatigue and muscle weakness.
25313769
MALE Middle Aged
Paraneoplastic dermatomyositis associated with adenocarcinoma of the lung.
Bursac DS, Sazdanic-Velikic DS, Tepavac AP, Secen NM.
J Cancer Res Ther. 2014;10(3):730-2.
The case of a 57-year old patient with lung adenocarcinoma and dermatomyositis as the first sign of the illness is presented.
22328959
OTHER
Dermatomyositis and metastatic lung adenocarcinoma first presenting as calcinosis cutis.
Lee GL, Anetakis Poulos G, J Zirwas M.
J Clin Aesthet Dermatol. 2012;5(1):47-8.
The authors report a case of dystrophic calcinosis cutis that ultimately led to the diagnosis of dermatomyositis and metastatic lung adenocarcinoma.
18545831
MALE
Lung adenocarcinoma, dermatomyositis, and Lambert-Eaton myasthenic syndrome: a rare combination.
Milanez FM, Pereira CA, Trindade PH, Milinavicius R, Coletta EN.
J Bras Pneumol. 2008;34(5):333-6.
Lung adenocarcinoma, dermatomyositis, and Lambert-Eaton myasthenic syndrome: a rare combination.
18545831
MALE
Lung adenocarcinoma, dermatomyositis, and Lambert-Eaton myasthenic syndrome: a rare combination.
Milanez FM, Pereira CA, Trindade PH, Milinavicius R, Coletta EN.
J Bras Pneumol. 2008;34(5):333-6.
The overall analysis of the case and a review of the literature allow us to suggest that the clinical profile of the patient was a result of an overlap of two paraneoplastic syndromes (dermatomyositis and Lambert-Eaton myasthenic syndrome) secondary to lung adenocarcinoma.