Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Shujiro Hayashi"'
Publikováno v:
JEADV Clinical Practice, Vol 2, Iss 4, Pp 932-936 (2023)
Abstract There have been a few reported cases of erythema nodosum (EN) after coronavirus disease 2019 (COVID‐19) vaccination. A 48‐year‐old healthy woman was referred to our department with multiple erythematous nodules of varying sizes on her
Externí odkaz:
https://doaj.org/article/d8c47172fb354396ae0693a7a5f65b86
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 7 (2024)
Externí odkaz:
https://doaj.org/article/334567b0eaba425898f333e1e6b35439
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/38ff1580e19b472baabf5c0040821845
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 6, Iss 6, Pp 260-261 (2023)
In this paper, we bring hope to patients with mycosis fungoides (MF) with CD30+ large‐cell transformation (LCT), which is often a histological marker of poor prognosis and is associated with a mean 5‐year survival of
Externí odkaz:
https://doaj.org/article/e949420302aa48e08624371ab8363162
Autor:
Satoko Ishikawa, Shujiro Hayashi, Toshimi Sairenchi, Manabu Miyamoto, Shigemi Yoshihara, Gen Kobashi, Tomomi Yamaguchi, Tomoki Kosho, Ken Igawa
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Vascular-type Ehlers–Danlos syndrome (vEDS) is caused by collagen III deficit resulting from heterogeneous mutations in COL3A1, which occasionally causes sudden death due to arterial/visceral rupture. However, it is difficult to conduct
Externí odkaz:
https://doaj.org/article/9b22479ce4ba4e2580486fcb1f20d9a2
Publikováno v:
Journal of International Medical Research, Vol 51 (2023)
The primary symptom of urticarial vasculitis (UV), which is a histopathological leukocytoclastic vasculitis disease, is an eruption that resembles urticaria. Other organs may also experience accompanying symptoms. Lung lesions with UV are mostly obst
Externí odkaz:
https://doaj.org/article/0515740771e7437b9973cca351bce394
Autor:
Tomomi Yamaguchi, Shujiro Hayashi, So Nagai, Akihiko Uchiyama, Sei-Ichiro Motegi, Tomomi Fujikawa, Yuri Takiguchi, Tomoki Kosho
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
The Ehlers–Danlos Syndromes (EDS), a group of hereditary connective tissue disorders, were classified into 13 subtypes in the 2017 International Classification. Recently, a new subtype of EDS called classical-like EDS type 2 (clEDS2), which is caus
Externí odkaz:
https://doaj.org/article/1ff3241ae08b4512bdc48ea0b65d6820
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 5, Iss 3, Pp 94-96 (2022)
A 47‐year‐old woman with mixed connective tissue disease was treated with abatacept. After 2 months, a 3‐cm depression with atrophied surface was observed on her back, which had histopathological consistent with the symptoms of localized sclero
Externí odkaz:
https://doaj.org/article/9c9293a4d21a40b7bb3b96f886df684e
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 6, Iss 2, Pp 59-60 (2023)
There are a few reports in the literature implicating them in causing fixed drug eruption, the piperazine derivatives. In this case, although eszopiclone for insomnia medicinehas a piperazine ring, no eruption appeared so far. Oxatomide and hydroxyzi
Externí odkaz:
https://doaj.org/article/4a654925b8c84aa9adea0d87842e9354
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Vascular-type Ehlers–Danlos syndrome (vEDS) is an autosomal dominant inherited disorder caused by a deficit in collagen III as a result of heterogeneous mutations in the α1 type III collagen gene (COL3A1). Patients with vEDS often expe
Externí odkaz:
https://doaj.org/article/6897d02e74034619ad91cc8f46f55e4c