نتایج جستجو برای: malignant fibrous histiocytoma mfh

تعداد نتایج: 229665  

Journal: :The journal of the Japanese Practical Surgeon Society 1993

2011
Anastasios Katsourakis George Noussios Iosif Hadjis Neofitos Evangelou Efthimios Chatzitheoklitos

Malignant fibrous histiocytoma (MFH) of the small intestine is an extremely rare condition. It occurs most commonly in the extremities and the trunk. We report a case of a 67-year-old woman who admitted with fever, myalgia, and altered status. After thorough investigation, a tumor of the jejunum was found. The patient underwent complete surgical removal of the tumor. A diagnosis of MFN (undiffe...

2012
Kanya Honoki Hiromasa Fujii Yasuaki Tohma Toshifumi Tsujiuchi Akira Kido Shinji Tsukamoto Toshio Mori Yasuhito Tanaka

Mesenchymal stem cells (MSCs) are believed to be the cell of origin for most sarcomas including osteosarcoma and malignant fibrous histiocytoma (MFH/UPS). To identify the signaling pathways involved in sarcoma pathogenesis, we compared gene expression profiles in rat osteosarcoma and MFH cells with those in syngeneic rat MSCs. Analysis of genes that characterize MSCs such as CD44, CD105, CD73, ...

Journal: :Neurologia medico-chirurgica 2003
Ryo Ueda Takuro Hayashi Kaori Kameyama Kazunari Yoshida Takeshi Kawase

An 18-year-old woman presented with a malignant fibrous histiocytoma (MFH) originating in the orbit and invading the frontal and temporal base of the skull manifesting as exophthalmos and double vision that had persisted for 2 months. Magnetic resonance imaging revealed a tumor in the left orbit that extended as far as the frontal and temporal base of the skull. The tumor was treated by radical...

2013
Si-Qi Qiu Xiao-Long Wei Wen-He Huang Ming-Yao Wu Yun-Sheng Qin Yang-Kang Li Guo-Jun Zhang

We analyzed the clinicopathological features of 9 breast malignant fibrous histiocytoma (MFH) patients. Immunohistochemistry was used to make both diagnosis and differential diagnosis, and to identify prognostic factors. All tumors lacked epithelial markers but expressed mesenchymal markers, suggesting a mesenchymal origin. Of the five cases expressing Ki-67, two of three patients with axillary...

Journal: :Annals of nuclear medicine 2006
Mototaka Miyake Ukihide Tateishi Tetsuo Maeda Yasuaki Arai Tadashi Hasegawa Kazuro Sugimura

Diaphyseal medullary stenosis (DMS) is an extremely rare hereditary bone dysplasia, which was first described by Arnold in 1973. DMS has a high incidence of pleomorphic malignant fibrous histiocytoma (MFH). In this paper, we report the imaging findings of DMS with pleomorphic MFH of the bone, mainly describing 99mTc hydroxymethylenediphosphonate (HMDP) and thallium-201 (201Tl) chloride scintigr...

Journal: :Turkish neurosurgery 2012
Mevci Ozdemir Onur Ozgural Melih Bozkurt Fuat Mehmet Torun Aylin Okcu Heper Hakan Tuna

We describe herein a patient with primary intracerebral malignant fibrous histiocytoma (MFH) to demonstrate this very rare central nervous system tumor. A 42-year-old male was admitted to our institute with the complaints of headache and speech impairment. Magnetic resonance imaging (MRI) revealed a tumor consistent with meningioma and we decided the surgery. The tumor was excis...

Journal: :European journal of cancer 2006
Maija Tarkkanen Marcelo L Larramendy Tom Böhling Massimo Serra Claudia M Hattinger Aarne Kivioja Inkeri Elomaa Piero Picci Sakari Knuutila

Malignant fibrous histiocytoma (MFH) of bone is a rare, highly malignant tumour. As very little is known about its genetic alterations, 26 bone MFHs were analysed by comparative genomic hybridisation (CGH). Twenty-three tumours (89%) had DNA sequence copy number changes (mean, 7.2 changes per sample). Gains were more frequent than losses (gains:losses=2.5:1). Minimal common regions for the most...

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