Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Masayoshi Yamanaka"'
Autor:
Masahito Yasuda, Cong Shang, Masayoshi Yamanaka, Hiroo Amano, Norifumi Tsukamoto, Osamu Ishikawa, Sei‐ichiro Motegi
Publikováno v:
The Journal of dermatologyREFERENCES.
Publikováno v:
Pigment Cell & Melanoma Research. 33:591-600
Dyschromatosis symmetrica hereditaria (DSH) is a pigmentary genodermatosis caused by mutations in ADAR1. In this study, we performed mutation analysis on a family that included typical DSH patients. No mutations were found in any coding regions or ex
Publikováno v:
Australasian Journal of Dermatology. 58:145-149
Cutaneous collagenous vasculopathy (CCV) is a rare acquired idiopathic microangiopathy characterised by the progressive development of diffuse asymptomatic telangiectasias over the skin. Histologically, the presence of a thick hyaline collagenous wal
Publikováno v:
Journal of Civil Engineering and Architecture. 10
Publikováno v:
The Journal of Dermatology. 37:94-97
Livedoid vasculopathy (LV) is thought to be a thrombogenic disorder. Here, we report a case of LV presenting livedo reticularis with leg ulcers clinically and many thrombogenic cutaneous vessels histologically. These features strongly suggested the p
Autor:
Setsuko Tanaka, Michiko Hasegawa, Masayoshi Yamanaka, Osamu Ishikawa, Yayoi Nagai, Naoya Igarashi
Publikováno v:
European Journal of Dermatology. 19:057-060
Purpura and livedo are common cutaneous manifestations of microscopic polyangiitis (MPA); however, only a few clinical analyses focusing on the relationship between clinical symptoms and the affected vessels in the skin have been reported. We herein
Publikováno v:
The Journal of Dermatology. 35:21-24
We report a 58-year-old man with mycosis fungoides (MF) and occupational systemic sclerosis (SSc) induced by silica exposure. He was engaged in tunnel construction from the age of 18 to 33 years. He developed MF at the age of 30. Diagnosis of silicos
Autor:
Masayoshi Yamanaka, Yuko Tanaka, Akira Hasegawa, Akihiko Nakano, Chie Hashimoto, Osamu Ishikawa, Hideaki Yokoo, Yayoi Nagai, Yoichi Nakazato
Publikováno v:
The Journal of Dermatology. 34:769-772
We report an autopsy case of a 60-year-old Japanese woman who died 27 years after the onset of systemic sclerosis and 4 years after the diagnosis of pulmonary arterial hypertension. Oral administration of bosentan was effective in improving her dyspn
Autor:
Akihiko Uchiyama, Sei-ichiro Motegi, Sahori Kanai, Sayaka Toki, Masayoshi Yamanaka, Kazuya Yamada, Osamu Ishikawa
Publikováno v:
The Journal of dermatology. 42(3)
Localized scleroderma (LSc) primarily affects skin, whereas systemic sclerosis (SSc) affects skin and various internal organs. LSc and SSc are considered to be basically different diseases, and there is no transition between them. However, LSc and SS
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