Total: 13 |
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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. |
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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. |
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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. |
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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. |
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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. |