Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Ko Ron Chen"'
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 6, Iss 5, Pp 146-151 (2023)
Abstract Objectives We conducted this study to clarify the progress of cutaneous arteritis. Methods We examined 21 cases of cutaneous arteritis that were diagnosed at our hospital between 2005 and 2020. The male‐to‐female ratio was 1:6 with a mea
Externí odkaz:
https://doaj.org/article/32f87f76698948288025478d557ceb25
Autor:
Toshiyuki Yamamoto, Ko-Ron Chen
Publikováno v:
The American Journal of Dermatopathology. 45:435-436
Autor:
Toshiyuki Yamamoto, Ko-Ron Chen
Publikováno v:
Journal of Cutaneous Pathology
Cutaneous vasculitis can be classified into two types based on the affected vessel size: small vessel vasculitis predominantly affecting dermal venules, and muscular vessel vasculitis as found in cutaneous arteritis predominantly affecting arteries l
Publikováno v:
The American Journal of Dermatopathology. 41:832-834
Eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg-Strauss syndrome) is a rare systemic vasculitis affecting small- and medium-sized vasculature, associated with asthma and eosinophilia. Different levels of vasculitis in cutaneous le
Publikováno v:
Australasian Journal of Dermatology. 61
Autor:
Ko-Ron Chen, Toshiyuki Yamamoto
Publikováno v:
The American Journal of dermatopathology. 42(3)
Autor:
Takashi Sawai, Kensei Katsuoka, Masanari Kodera, Takaharu Ikeda, Naoko Ishiguro, Akiko Tanikawa, Fukumi Furukawa, Ko-Ron Chen, Takeshi Kono, Mariko Seishima, Tamihiro Kawakami, Yasuyuki Sawada, Minoru Hasegawa, Miwa Uzuki, Seiji Kawana, Shoichi Ozaki
Publikováno v:
The Journal of Dermatology. 45:122-127
The proposal by the 1994 International Chapel Hill Consensus Conference on the Nomenclature of Systemic Vasculitides (CHCC1994) and by the CHCC2012 markedly influenced the classification and way of considering cutaneous vasculitis. In the proposal by
Autor:
Ko-Ron Chen, Toshiyuki Yamamoto
Publikováno v:
The American Journal of Dermatopathology. 42:307-308
Publikováno v:
Clinical Case Reports
Key Clinical Message We reported a patient with systemic lupus erythematosus complicated by livedoid vasculopathy (LV), who responded well to intravenous immunoglobulin and warfarin. Cutaneous lesions of LV resemble those of cutaneous vasculitis. LV
Publikováno v:
The American Journal of Dermatopathology. 42:555-556