Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Teruto Isayama"'
Autor:
Yuichi Yamada, Teruto Isayama, Masakazu Toya, Kazuki Nabeshima, Ryohei Yokoyama, Yoshinao Oda, Kenichi Taguchi
Publikováno v:
Pathology - Research and Practice. 216:152832
Low-grade central osteosarcoma (LG-COS) is an uncommon variant of osteosarcoma (OS) that sometimes progresses to high-grade OS post-recurrence. We herein present a case of dedifferentiated LG-COS with extensive cystic change arising in the right ilia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adf909e869596e9d7523318a703ac68b
https://doi.org/10.1016/j.prp.2020.152832
https://doi.org/10.1016/j.prp.2020.152832
Publikováno v:
Journal of Shoulder and Elbow Surgery. 21:77-81
Background Elastofibroma typically occurs in the subscapular region of elderly individuals and has a high incidence in Kyushu and the surrounding islands in southern Japan. The treatment of this lesion is somewhat controversial. Patients and methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b3c0a336c24a1c4e11bd105f2b67cf5
https://doi.org/10.1016/j.jse.2011.01.043
https://doi.org/10.1016/j.jse.2011.01.043
Publikováno v:
Orthopedics & Traumatology. 60:210-215
両側進行・末期変形性股関節症に両側に大腿骨骨切り術併用のキアリ手術を施行し，2年以上経過を観察した症例について，除痛に成功したかどうかを検討した．対象となる20例（男性3例
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ebe80c64db64cae626f5213485beeb4
https://doi.org/10.5035/nishiseisai.60.210
https://doi.org/10.5035/nishiseisai.60.210
Autor:
Michihisa Zenmyo, Tetsuya Hamada, Nobuhiro Fukushima, Kensei Nagata, Akihiko Yoshimura, Hiroshi Iwasaki, Setsuro Komiya, Teruto Isayama, Takanori Shouda, Koji Hiraoka
Publikováno v:
Cancer Letters. 231:176-184
There is no established optimum treatment for malignant fibrous histiocytoma (MFH) at present, and few MFH cell lines are established. In the present study, we established new MFH cell lines, KHZ-MFH and SFT85-03, and investigated the JAK/STAT (Janus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4e2459ba3616a7e3a34451c17e63ccc
https://doi.org/10.1016/j.canlet.2005.01.042
https://doi.org/10.1016/j.canlet.2005.01.042
Autor:
Masahiro Kikuchi, Seiji Haraoka, Masatoshi Naito, Jun Nishio, Teruto Isayama, Haruhiko Miyayama, Yuuya Yamashita, Naomi Sakashita, Hiroshi Iwasaki
Publikováno v:
Human Pathology. 34:246-252
Undifferentiated (embryonal) sarcoma of the liver (UESL) is a rare pediatric liver malignancy that is extremely uncommon in middle-aged individuals. We studied 2 cases of UESL in middle-aged adults (1 case in a 49-year-old woman and the other in a 62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e0a2fc7e8bf6cac98bcd5b7c5004063
https://doi.org/10.1053/hupa.2003.44
https://doi.org/10.1053/hupa.2003.44
Autor:
Hiroshi Iwasaki, Nanao Kamada, Yasuhiko Kaneko, Yuko Ohjimi, Masako Ishiguro, Masahiro Kikuchi, Jun Nishio, Masatoshi Naito, Teruto Isayama
Publikováno v:
Cancer Genetics and Cytogenetics. 137:23-28
A consistent, pathognomonic translocation, most commonly a balanced reciprocal translocation, t(X;18) (p11.2;q11.2), is found in more than 90% of synovial sarcomas. We report here a secondary chromosome change, der(22)t(17;22)(q12;q12), in addition t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::560c827d7b7d589ca89144ddda9f798c
https://doi.org/10.1016/s0165-4608(02)00550-2
https://doi.org/10.1016/s0165-4608(02)00550-2
Autor:
Masahiro Kikuchi, Yuko Ohjimi, Teruto Isayama, Yasuhiko Kaneko, Jun Nishio, Hiroshi Iwasaki, Masako Ishiguro, Masatoshi Naito, Hiroshi Okabayashi
Publikováno v:
Cancer Genetics and Cytogenetics. 133:124-128
Ossifying fibromyxoid tumor (OFMT) of soft parts is a recently described, rare but morphologically distinctive soft tissue tumor. The histogenesis of this lesion remains uncertain, although several immunohistochemical and ultrastructural features sug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1ef21d96af25b1faa34a338abe54d2e
https://doi.org/10.1016/s0165-4608(01)00581-7
https://doi.org/10.1016/s0165-4608(01)00581-7
Autor:
Yuko Ohjimi, Masahiro Kikuchi, Hiroshi Iwasaki, Akinori Iwashita, Masako Ishiguro, Jun Nishio, Teruto Isayama, Masatoshi Naito
Publikováno v:
Cancer Genetics and Cytogenetics. 132:102-108
Histopathological differentiation between dermatofibrosarcoma protuberans (DFSP) and dermatofibroma (DF) is often difficult, because both neoplasms share some clinical features and the presence of a storiform pattern. In the present study, we investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9ef68e31213a22c6b13fd72a70b71cf
https://doi.org/10.1016/s0165-4608(01)00546-5
https://doi.org/10.1016/s0165-4608(01)00546-5
Autor:
Jun Nishio, Yasuhiko Kaneko, Masatoshi Naito, Masako Ishiguro, Masahiro Kikuchi, Yuko Ohjimi, Teruto Isayama, Hiroshi Iwasaki
Publikováno v:
Cancer Genetics and Cytogenetics. 129:102-106
Dermatofibrosarcoma protuberans (DFSP) presents with characteristic cytogenetic features such as reciprocal t(17;22)(q22;q13) or, more commonly, supernumerary ring chromosomes containing sequences from chromosomes 17 and 22. Here, we report the ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1424eb6af9ccc7db41be3a01dedbc1d5
https://doi.org/10.1016/s0165-4608(01)00447-2
https://doi.org/10.1016/s0165-4608(01)00447-2
Autor:
Yuko Ohjimi, Masahiro Kikuchi, Akinori Iwashita, Masatoshi Naito, Hiroshi Iwasaki, Koji Yamakawa, Teruto Isayama
Publikováno v:
Pathology - Research and Practice. 197:499-506
We describe five cases of tumoral calcium pyrophosphate dihydrate crystal deposition disease (CPPDCD) and discuss the clinical, radiological and pathological features. Patients included 4 males and 1 female, ranging in age from 49 to 70 years (median
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a6068d53392e522d87d37cc09dc5290
https://doi.org/10.1078/0344-0338-00118
https://doi.org/10.1078/0344-0338-00118