scholarly journals Early skin reaction following 250MeV proton peak irradiation.

1987 ◽  
Vol 28 (2) ◽  
pp. 150-155 ◽  
Author(s):  
HIDEO TATSUZAKI ◽  
TETSUO INADA ◽  
TAKESHI SHIMIZU ◽  
TAKURO ARIMOTO ◽  
SHINICHIRO SATOH ◽  
...  
Keyword(s):  
Skin Reaction ◽  
Proton Peak

Asians on Phenytoin at High Skin Reaction Risk

2009 ◽  
Vol 39 (2) ◽  
pp. 17
Author(s):  
ELIZABETH MECHCATIE
Keyword(s):  
Skin Reaction

Toxicities of axitinib, sunitinib and temsirolimus: implications for progression-free and overall survival in metastatic renal cell cancer

2020 ◽  
Author(s):  
Annemarie Uhlig ◽  
Johannes Uhlig ◽  
Lutz Trojan ◽  
Michael Woike ◽  
Marianne Leitsmann ◽  
...  
Keyword(s):  
Overall Survival ◽  
Cancer Patients ◽  
Skin Reaction ◽  
Renal Cell Cancer ◽  
Renal Cell ◽  
Cell Cancer ◽  
Progression Free Survival ◽  
Cox Models ◽  
Metastatic Renal Cell Cancer ◽  
Hand Foot Skin Reaction

The aim of this study was to evaluate the association between axitinib, sunitinib and temsirolimus toxicities and patient survival in metastatic renal cell cancer patients. Overall survival (OS) and progression-free survival (PFS) of metastatic renal cell cancer patients from the prospective multicenter STAR-TOR study were assessed using multivariable Cox models. A total of 1195 patients were included (n = 149 axitinib; n = 546 sunitinib; n = 500 temsirolimus). The following toxicities significantly predicted outcomes: hand–foot skin reaction (hazard ratio [HR] = 0.29) for PFS with axitinib; stomatitis (HR = 0.62) and pneumonitis (HR = 0.23) for PFS with temsirolimus; stomatitis (HR = 0.52) and thrombocytopenia (HR = 0.6) for OS with temsirolimus; fatigue (HR = 0.71) for PFS with sunitinib; hand–foot skin reaction (HR = 0.56) and fatigue (HR = 0.58) for OS with sunitinib. In conclusion, in metastatic renal cell cancer, axitinib, sunitinib and temsirolimus demonstrate specific toxicities that are protective OS/PFS predictors.

Triamcinolone pretreatment decreases skin reaction severity seen with transdermal testosterone,

1998 ◽  
Vol &NA; (703) ◽  
pp. 4
Author(s):  
&NA;
Keyword(s):  
Skin Reaction ◽  
Reaction Severity

Observations on a Delayed Skin Reaction to Cold

1932 ◽  
Vol 29 (8) ◽  
pp. 936-936
Author(s):  
M. H. Saier ◽  
W. C. Van Deventer ◽  
G. D. Barnett
Keyword(s):  
Skin Reaction

scholarly journals Aripiprazole induced severe and extensive skin reaction: A case report

2012 ◽  
Vol 2 (5) ◽  
pp. 195-198 ◽  
Author(s):  
Caroline Parker
Keyword(s):  
Case Report ◽  
Skin Reaction

A further case of adverse skin reaction from vitamin Ki

1977 ◽  
Vol 97 (6) ◽  
pp. 697-697 ◽  
Author(s):  
G. HEYDENREICH
Keyword(s):  
Skin Reaction

scholarly journals Dabigatran Associated Leukocytoclastic Vasculitis

2015 ◽  
Vol 2015 ◽  
pp. 1-2 ◽  
Author(s):  
Evangelos Potolidis ◽  
Charalampos Mandros ◽  
Kalliopi Kotsa ◽  
Evdoxia Mitsiou ◽  
Dimitris Potolidis ◽  
...  
Keyword(s):  
Side Effects ◽  
Skin Biopsy ◽  
Skin Reaction ◽  
Leukocytoclastic Vasculitis ◽  
Skin Reactions ◽  
Usual Therapy

Common side effects of dabigatran are bleeding, bruising, nausea, diarrhea, and abdomen discomfort. Skin reactions were not often noted (<0.1%). We report a case of 70-year-old male who developed dabigatran related skin reaction resistant to usual therapy. Skin biopsy revealed leukocytoclastic vasculitis.

Murine auricular transepidermal water loss − a novel approach for evaluating irritant skin reaction in mice

2001 ◽  
Vol 26 (2) ◽  
pp. 196-200 ◽  
Author(s):  
H. Löffler ◽  
R. Hoffmann ◽  
R. Happle ◽  
I. Effendy
Keyword(s):  
Skin Reaction ◽  
Water Loss ◽  
Transepidermal Water Loss ◽  
Novel Approach
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