scholarly journals Anti-transcription intermediary factor 1 gamma (TIF1γ) antibody-positive dermatomyositis associated with ascending colon cancer: a case report and review of the literature

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Ryohei Ono ◽  
Tomohiro Kumagae ◽  
Mari Igasaki ◽  
Takaaki Murata ◽  
Masaki Yoshizawa ◽  
...  

Abstract Background Anti-transcriptional intermediary factor 1 gamma (TIF1γ) antibody is a marker for predicting cancer association in patients with dermatomyositis (DM). The overall survival rate in DM patients with cancer was reported to be considerably worse than that in DM patients without cancer. However, the treatment for cancer-associated DM remains controversial, because the treatment priority between surgical resection for the tumor and internal treatments, including glucocorticoids, immunosuppressive agents, and intravenous immune globulin, has not been established. Case presentation We report the case of a 57-year-old Japanese man diagnosed with anti-TIF1γ antibody-positive DM associated with ascending colon cancer. His clinical symptoms included facial and brachial edema, muscle weakness, dysphagia, myalgia, and rash. Physical examination revealed periorbital edema and Gottron's papules over his knuckles with brachial edema, and tenderness and weakness of the proximal limb muscles. The findings of hyperintense muscles in T2-weighted sequences of brachial contrast-enhanced magnetic resonance imaging and the infiltration of lymphocytic cells and CD4-positive lymphocytes from muscle biopsy were compatible with the diagnostic criteria for dermatomyositis. Anti-TIF1γ antibody was positive by immunoprecipitation assay. He first started internal treatment including intravenous immunoglobulin, steroid pulse, prednisolone, and azathioprine, followed by surgical resection for the tumor because of the elevation of creatine kinase and progression of dysphagia. However, clinical symptoms did not improve, and the patient died 6 months later. Conclusions We faced difficulties in determining the treatment priority between surgical resection and internal treatment for our case; therefore, this case would be educational for readers. We searched PubMed to identify English-language case reports of anti-TIF1γ antibody-positive dermatomyositis with malignancy and found 21 reported cases. We herein review and summarize previously reported cases of anti-TIF1γ antibody-positive DM with malignancy. Cancer screening is essential in patients with anti-TIF1γ antibody-positive dermatomyositis because it is associated with a high prevalence of malignancies. Our review revealed that initial surgical treatment should be recommended for better prognosis if the general condition allows.

2020 ◽  
Vol 22 (1) ◽  
pp. 32-45
Author(s):  
Emanuela Martina ◽  
Federico Diotallevi ◽  
Tommaso Bianchelli ◽  
Matteo Paolinelli ◽  
Annamaria Offidani

Background: Chronic Spontaneous Urticaria (CSU) is a disease characterized by the onset of wheals and/or angioedema over 6 weeks. The pathophysiology for CSU is very complex, involving mast cells and basophils with a multitude of inflammatory mediators. For many years the treatment of CSU has been based on the use of antihistamines, steroids and immunosuppressive agents with inconstant and frustrating results. The introduction of omalizumab, the only licensed biologic for antihistamine- refractory CSU, has changed the management of the disease. Objective: The aim of this article is to review the current state of the art of CSU, the real-life experience with omalizumab and the promising drugs that are under development. Methods:: An electronic search was performed to identify studies, case reports, guidelines and reviews focused on the new targets for the treatment of chronic spontaneous urticaria, both approved or under investigation. The search was limited to articles published in peer-reviewed journals in the English Language in the PubMed database and trials registered in Clinicaltrials.gov. Results:: Since the advent of omalizumab, the search for new therapies for chronic spontaneous urticaria has had a new impulse. Anti-IgE drugs will probably still be the cornerstone of therapy, but new targets may prove effective in syndromic urticaria or refractory cases. Conclusion:: Although omalizumab has been a breakthrough in the treatment of CSU, many patients do not completely get benefit and even require more effective treatments. Novel drugs are under investigation with promising results.


2015 ◽  
Vol 106 (4) ◽  
pp. 264-268
Author(s):  
Ryuichi Nishiyama ◽  
Masashi Kubota ◽  
Toru Kanno ◽  
Takashi Okada ◽  
Yoshihito Higashi ◽  
...  

2015 ◽  
Vol 76 (11) ◽  
pp. 2749-2753
Author(s):  
Yoshihiro MIYAGI ◽  
Ayano TSUTSUMI ◽  
Shingo TSUTSUMI ◽  
Michinaru AKAMATSU ◽  
Takao HIGA ◽  
...  

2012 ◽  
Vol 73 (10) ◽  
pp. 2606-2609
Author(s):  
Takanobu YAMADA ◽  
Insop HAN ◽  
Yasuyuki JIN ◽  
Kimiatsu HASUO ◽  
Yasushi RINO ◽  
...  

1996 ◽  
Vol 49 (0) ◽  
pp. 216-217
Author(s):  
Yasuhiro Onozato ◽  
Izuru Kobayashi ◽  
Hiroshi Ishihara ◽  
Makoto Yoshida ◽  
Kenta Motegi ◽  
...  

2012 ◽  
Vol 62 (3) ◽  
pp. 295-299
Author(s):  
Hotaka Yamazaki ◽  
Keitaro Hirai ◽  
Daisuke Yoshinari ◽  
Kei Komatsu ◽  
Taisuke Sato ◽  
...  

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