Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Mayumi Katoh"'
Publikováno v:
The Journal of Dermatology. 43:1301-1306
Eosinophilic pustular folliculitis (EPF) is a sterile inflammatory dermatosis of unknown etiology. In addition to classic EPF, which affects otherwise healthy individuals, an immunocompromised state can cause immunosuppression-associated EPF (IS-EPF)
Publikováno v:
The Journal of dermatology. 43(7)
Autor:
Ayako Kojima, Satoshi Kore-Eda, Yumi Matsumura, Mayumi Katoh, Mami Sato, Chisa Nakashima, Yoshiki Miyachi
Publikováno v:
The Journal of Dermatology. 38:1037-1040
Publikováno v:
The Journal of dermatology. 43(8)
Eosinophilic pustular folliculitis (EPF) is a non-infectious inflammatory dermatosis of unknown etiology that principally affects the hair follicles. There are three variants of EPF: (i) classic EPF; (ii) immunosuppression-associated EPF, which is su
Publikováno v:
The Journal of Dermatology. 31:403-406
Chemotherapy-induced acral erythema (CIAE) is a rare cutaneous reaction to high-dose chemotherapy, clinically featuring painful erythema on the palms and soles. Docetaxel (Taxotere), an anticancer agent, is known to cause various reactions, including
Publikováno v:
Dermato-Endocrinology. 1:43-45
We reviewed the causes of "loss of skin color" in 144 patients, who visited Vitiligo Clinic of Kyoto University Hospital between April 2005 and August 2008. The numbers of patients with generalized and segmental Vitiligo vulgaris were 98 (68.1%) and
Publikováno v:
The Journal of dermatology. 40(1)
Eosinophilic pustular folliculitis (EPF), also known as Ofuji's disease, is an inflammatory dermatosis that was first described in Japan in 1970. More than 300 cases have been reported so far, and 113 Japanese cases have been reported in Japan since
Publikováno v:
Ueda, Miho; Katoh, Mayumi; Tanizaki, Hideaki; Tanioka, Miki; Matsumura, Yumi; & Miyachi, Yoshiki. (2012). Refractory pyoderma gangrenosum associated with ulcerative colitis successfully treated with infliximab. Dermatology Online Journal, 18(1). Retrieved from: http://www.escholarship.org/uc/item/9c8094s3
Pyoderma gangrenosum (PG) is a rare, immune-mediated ulcerating skin disease. In up to 50 percent of the cases, PG is associated with underlying systemic disorders, most commonly inflammatory bowel diseases, connective tissue diseases, or hematologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f36018a947b30012d5fe0cdb9497668
http://www.escholarship.org/uc/item/9c8094s3
http://www.escholarship.org/uc/item/9c8094s3
Publikováno v:
The Journal of Dermatology.
Publikováno v:
The Journal of Dermatology. 41:447-448