Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hiroyuki Fujii, MD"'
Autor:
Yuriko Watanabe, MD, Hiroyuki Fujii, MD, PhD, Saki Yamamoto, MD, Sota Masuoka, MD, Ryoma Kobayashi, MD, Nana Fujii, MD, Akihiro Nakamata, MD, Takeharu Kanazawa, MD, PhD, Mitsuru Matsuki, MD, PhD, Harushi Mori, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 6141-6146 (2024)
Mucosa-associated lymphoid tissue (MALT) lymphoma commonly arises from chronic inflammation or autoimmune diseases, such as Sjögren syndrome (SjS). Although rare, amyloid deposition in MALT lymphoma has been reported. We present a rare case of parot
Externí odkaz:
https://doaj.org/article/d9c7a9ad07fc4343a63e512dc00cf168
Autor:
Hiroyuki Fujii, MD, PhD, Mitsuru Matsuki, MD, PhD, Takefumi Hamakawa, MD, Yumiko Toda, MD, Nana Fujii, MD, Sota Masuoka, MD, Akihiro Nakamata, MD, Emiko Chiba, MD, PhD, Kazunari Ishii, MD, PhD, Harushi Mori, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 5, Pp 1666-1670 (2024)
Hemochromatosis is a primary or secondary pathological condition characterized by the deposition of excess iron in the body tissues, which can eventually lead to cellular damage and organ dysfunction. Although excess iron deposition in the central ne
Externí odkaz:
https://doaj.org/article/e79045a17d4d49558f1f7aa780c618ca
Autor:
Yuki Katayama, MD, PhD, Tadaaki Yamada, MD, PhD, Kenji Morimoto, MD, PhD, Hiroyuki Fujii, MD, Satomi Morita, MD, PhD, Keiko Tanimura, MD, PhD, Takayuki Takeda, MD, PhD, Asuka Okada, MD, PhD, Shinsuke Shiotsu, MD, PhD, Yusuke Chihara, MD, PhD, Osamu Hiranuma, MD, Takahiro Yamada, MD, PhD, Takahiro Ota, MD, PhD, Taishi Harada, MD, Isao Hasegawa, MD, PhD, Masahiro Iwasaku, MD, PhD, Shinsaku Tokuda, MD, PhD, Noriyuki Tanaka, MD, PhD, Aya Miyagawa-Hayashino, MD, PhD, Koichi Takayama, MD, PhD
Publikováno v:
JTO Clinical and Research Reports, Vol 5, Iss 3, Pp 100644- (2024)
Introduction: Multiple programmed death-ligand 1 (PD-L1) immunohistochemistry assays performed using different antibodies including DAKO 22C3, DAKO 28-8, and Ventana SP142 PD-L1—predictive markers for response to various immune checkpoint inhibitor
Externí odkaz:
https://doaj.org/article/3964141379334812bbe15faf7291e902
Autor:
Nana Fujii, MD, Hiroyuki Fujii, MD, PhD, Mitsuru Matsuki, MD, PhD, Shugo Doi, MD, Takenori Isozaki, MD, Yuriko Watanabe, MD, Akihiro Nakamata, MD, Akifumi Fujita, MD, PhD, Harushi Mori, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 10, Pp 3769-3772 (2023)
Posterior reversible encephalopathy syndrome (PRES) is a clinico-radiological condition characterized by reversible vasogenic edema of the white matter and acute neurological symptoms. PRES typically affects the parieto-occipital regions but rarely a
Externí odkaz:
https://doaj.org/article/0d201e8a64c34d618d584a914a016d74
Autor:
Hiroyuki Fujii, MD, PhD, Tadahide Noguchi, DDS, PhD, Tamaki Miura, MD, Nana Fujii, MD, Takenori Isozaki, MD, Akifumi Fujita, MD, PhD, Toshiro Niki, MD, PhD, Mitsuru Matsuki, MD, PhD, Harushi Mori, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 10, Pp 3626-3631 (2023)
Sclerosing microcystic adenocarcinoma (SMA) is a rare malignant tumor of the salivary glands that closely resembles cutaneous microcystic adnexal carcinoma (MAC). It was newly listed in the 5th edition of the WHO classification of head and neck tumor
Externí odkaz:
https://doaj.org/article/ac138f62d891460caa66c8ea195757ea
Autor:
Ryo Tateishi, MD, Hiroshi Shimada, MD, Hiroyuki Fujii, MD, Makoto Suzuki, MD, PhD, Mitsuhiro Nishizaki, MD, PhD, Tetsuo Sasano, MD, PhD
Publikováno v:
HeartRhythm Case Reports, Vol 8, Iss 9, Pp 622-626 (2022)
Externí odkaz:
https://doaj.org/article/6008ee17c4234780ad0400fabfb45cfc
Autor:
Ryota Nakamura, MD, Hiroyuki Fujii, MD, Tadaaki Yamada, MD, PhD, Yohei Matsui, MD, Takeshi Yaoi, MS, Mizuki Honda, MD, Noriyuki Tanaka, MD, PhD, Aya Miyagawa-Hayashino, MD, PhD, Akihiro Yoshimura, MD, PhD, Kenji Morimoto, MD, PhD, Masahiro Iwasaku, MD, PhD, Shinsaku Tokuda, MD, PhD, Young Hak Kim, MD, PhD, Eiichi Konishi, MD, PhD, Kyoko Itoh, MD, PhD, Koichi Takayama, MD, PhD
Publikováno v:
JTO Clinical and Research Reports, Vol 4, Iss 6, Pp 100525- (2023)
Introduction: EGFR tyrosine kinase inhibitors are standard therapeutic agents for patients with advanced NSCLC harboring EGFR mutations. Nevertheless, some patients exhibit primary resistance to EGFR tyrosine kinase inhibitors in the first-line treat
Externí odkaz:
https://doaj.org/article/27b3e58854a34814b01a239b63d7e6ea
Autor:
Yuki Katayama, MD, Tadaaki Yamada, MD, PhD, Kenji Morimoto, MD, PhD, Hiroyuki Fujii, MD, Satomi Morita, MD, Keiko Tanimura, MD, PhD, Takayuki Takeda, MD, PhD, Asuka Okada, MD, PhD, Shinsuke Shiotsu, MD, PhD, Yusuke Chihara, MD, PhD, Osamu Hiranuma, MD, Takahiro Yamada, MD, PhD, Takahiro Ota, MD, PhD, Taishi Harada, MD, Isao Hasegawa, MD, PhD, Akihiro Yoshimura, MD, PhD, Masahiro Iwasaku, MD, PhD, Shinsaku Tokuda, MD, PhD, Young Hak Kim, MD, PhD, Koichi Takayama, MD, PhD
Publikováno v:
JTO Clinical and Research Reports, Vol 4, Iss 4, Pp 100494- (2023)
Introduction: Lung adenocarcinoma with negative TTF-1 expression is believed to be a poor prognostic factor for certain systemic treatments. Nevertheless, the impact of TTF-1 expression on combined chemoimmunotherapy remains unclear. We aimed to inve
Externí odkaz:
https://doaj.org/article/f5a29b79c158468da31bfa4f00a93ada
Autor:
Masashi Endo, MD, Hiroyuki Fujii, MD, PhD, Akifumi Fujita, MD, PhD, Tatsuya Takayama, MD, PhD, Daisuke Matsubara, MD, PhD, Tomohiro Kikuchi, MD, Saki Manaka, MD, Harushi Mori, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 3, Pp 619-622 (2022)
Ectopic adrenocortical tissue can arise along the path of embryonic migration, such as the celiac axis, broad ligament, adnexa of the testis, and spermatic cord. Occasionally, ectopic adrenocortical tissues undergo marked hyperplasia and develop into
Externí odkaz:
https://doaj.org/article/bbfaa3bd9456489f8eb401db98d5edf1
Autor:
Atsushi Ugajin, MD, Hiroyuki Fujii, MD,PhD, Akifumi Fujita, MD,PhD, Hiroyasu Nakamura, MD, Akira Fujisaki, MD, Hideharu Sugimoto, MD,PhD
Publikováno v:
Radiology Case Reports, Vol 15, Iss 3, Pp 285-291 (2020)
We describe the case of an adult female with a huge pelvic arteriovenous malformation (AVM) measuring approx. 8 × 10 × 13 cm, treated via the transvenous approach alone. Management of huge pelvic AVMs is challenging; there is no consensus on a stan
Externí odkaz:
https://doaj.org/article/fe461d289e9543188e9593074f50738d