Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Kaoru HIRABAYASHI"'
Autor:
Akira Maejima, Toru Hirozane, Sayaka Yamaguchi, Tomoaki Mori, Naofumi Asano, Kazutaka Kikuta, Kaoru Hirabayashi, Katsuhito Takeuchi, Robert Nakayama, Masaya Nakamura, Morio Matsumoto
Publikováno v:
Case Reports in Oncology, Vol 16, Iss 1, Pp 1223-1231 (2023)
Atypical lipomatous tumor/well-differentiated liposarcoma (ALT/WDLPS) is usually a solitary adipocytic tumor. ALT/WDLPS shows no potential for metastasis unless it undergoes dedifferentiation. No case of multiple ALT/WDLPS has been reported in recent
Externí odkaz:
https://doaj.org/article/bd342eb8fb6f485aae9b442dc4dd6750
Autor:
Makoto Abe, Nobuo Hoshi, Sayuri Hoshi, Kaoru Hirabayashi, Kazutaka Kikuta, Toru Hirozane, Rumi Nakagawa, Tsukasa Mizuno, Hiroshi Nakamura, Koichi Inoue, Takehiko Yamaguchi
Publikováno v:
Case Reports in Pathology, Vol 2023 (2023)
Pleomorphic liposarcoma is a rare malignant adipocytic tumor showing undifferentiated pleomorphic sarcoma morphology with various degrees of epithelioid features. It is sometimes difficult to distinguish from carcinoma metastasis. Immunohistochemical
Externí odkaz:
https://doaj.org/article/d128c6a833c447e98aee578f209edafb
Autor:
Naoko Asano, Tomohiro Kinoshita, Jun-Ichi Tamaru, Koichi Ohshima, Tadashi Yoshino, Nozomi Niitsu, Norifumi Tsukamoto, Kaoru Hirabayashi, Koji Izutsu, Masafumi Taniwaki, Yasuo Morishima, Shigeo Nakamura
Publikováno v:
Haematologica, Vol 96, Iss 11 (2011)
Background Classical Hodgkin’s lymphoma is characterized by Hodgkin and Reed Sternberg cells, which are of B-cell origin in many cases. We recently highlighted the adverse prognostic significance of cytotoxic molecule expression in patients with cl
Externí odkaz:
https://doaj.org/article/b9a83613ddc9441686abcf16fc80572b
Autor:
Yuki Yoshimatsu, Rei Noguchi, Yooksil Sin, Ryuto Tsuchiya, Takuya Ono, Taro Akiyama, Rumi Nakagawa, Satoshi Kamio, Kaoru Hirabayashi, Iwao Ozawa, Kazutaka Kikuta, Tadashi Kondo
Publikováno v:
Human Cell. 35:1270-1278
Dedifferentiated liposarcoma (DDLPS) is morphologically characterized by well-differentiated liposarcomas associated with high-grade non-lipogenic sarcoma and molecularly characterized by the coamplification of MDM2 and CDK4(12q14-15). DDLPS is highl
Autor:
Yuki Yoshimatsu, Rei Noguchi, Yooksil Sin, Ryuto Tsuchiya, Takuya Ono, Taro Akiyama, Rumi Nakagawa, Satoshi Kamio, Kaoru Hirabayashi, Iwao Ozawa, Kazutaka Kikuta, Tadashi Kondo
Publikováno v:
Human Cell. 35:1262-1269
Ewing sarcoma (ES) is a small round cell sarcoma that is characterized by the unique gene translocation EWSR1-FLI1. It is the second most common primary bone and soft tissue malignancy in children and adolescents. It constitutes 10-15% of all bone sa
Autor:
Kaori UETA, Nobuo HOSHI, Masaru SASAKI, Kimiko NAKANO, Makoto ABE, Sayuri HOSHI, Kaoru HIRABAYASHI
Publikováno v:
The Journal of the Japanese Society of Clinical Cytology. 61:122-128
Autor:
Rei Noguchi, Takuya Ono, Tadashi Kondo, Yooksil Sin, Kazutaka Kikuta, Yuki Yoshimatsu, Iwao Ozawa, Ryuto Tsuchiya, Kaoru Hirabayashi, Rumi Nakagawa
Publikováno v:
Human Cell. 35:392-399
Giant cell tumor of bone (GCTB) is a rare osteolytic intermediate bone tumor that harbors a pathogenic H3F3A gene mutation and exhibits characteristic histology. The standard curative treatment for GCTB is complete surgical resection, but it frequent
Autor:
Rei Noguchi, Iwao Ozawa, Akane Sei, Takuya Ono, Yuki Yoshimatsu, Kaoru Hirabayashi, Tadashi Kondo, Kazutaka Kikuta
Publikováno v:
Human Cell. 34:990-997
Dedifferentiated liposarcoma (DDLPS) is a highly aggressive subtype of liposarcoma that is histologically a transition form between an atypical lipomatous tumor/well-differentiated liposarcoma and a non-lipogenic sarcoma. DDLPS is genetically charact
Autor:
Rei Noguchi, Yuki Yoshimatsu, Yooksil Sin, Ryuto Tsuchiya, Takuya Ono, Taro Akiyama, Kaoru Hirabayashi, Iwao Ozawa, Rumi Nakagawa, Kazutaka Kikuta, Tadashi Kondo
Publikováno v:
Human cell. 35(4)
Myxoid liposarcoma (MLPS) is a lipogenic sarcoma, characterized by myxoid appearance histology and the presence of the FUS-DDIT3 fusion gene. MLPS shows frequent recurrence and poor prognosis after standard treatments, such as surgery. Therefore, nov
Autor:
Kaoru Hirabayashi, Kazutaka Kikuta, Rei Noguchi, Yuki Yoshimatsu, Takuya Ono, Tadashi Kondo, Akane Sei, Iwao Ozawa
Publikováno v:
Human Cell. 34:688-697
Pleomorphic liposarcoma (PLPS) is a rare subtype of liposarcoma, characterized by the presence of pleomorphic lipoblasts without definitive molecular aberrations; it accounts for less than 5% of all liposarcomas. PLPS is an aggressive cancer that exh