癌診療指針のための病理診断プラクティス　骨・軟部腫瘍

出版社： 中山書店
著者：
発行日： 2013-12-10
分野： 臨床医学：一般  >  癌/腫瘍一般
ISBN： 9784521736754
シリーズ： 癌診療指針のための病理診断プラクティス
電子書籍版： 2013-12-10 （初版第1刷）
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2013年春に改訂されたばかりのWHO分類に準拠．さまざまな部位から発生するために種類が多い骨・軟部腫瘍の鑑別を助ける,フローチャートや豊富な病理写真を掲載．骨腫瘍では単純X線写真も収載し,病理医だけではなく,整形外科医にもお勧め．

目次

  • 癌診療指針のための病理診断プラクティス　骨・軟部腫瘍

    ―目次―

    1章　病理診断の流れとポイント

    2章　診断のための基本知識
    　骨腫瘍の画像診断
    　軟部腫瘍の画像診断
    　骨腫瘍の病理診断と治療
    　軟部腫瘍の病理診断と治療
    　骨軟部腫瘍の組織学的悪性度とgrading

    3章　骨腫瘍の概要と鑑別診断
    　良性骨形成性腫瘍
    　悪性の骨形成性腫瘍
    　　　髄内
    　　　表在性
    　良性軟骨形成性腫瘍
    　悪性軟骨形成性腫瘍
    　骨悪性線維性組織球腫
    　Ewing肉腫/PNET
    　悪性リンパ腫と多発性骨髄腫
    　脊索腫
    　骨巨細胞腫
    　その他の巨細胞性腫瘍類似病変
    　fibroosseous leusion

    4章　軟部腫瘍の概要と鑑別診断
    　脂肪肉腫
    　結節性筋膜炎とfasciitis lesion
    　デスモイド型線維腫症
    　隆起性皮膚線維肉腫
    　孤立性線維性肉腫
    　粘液線維肉腫
    　腱鞘巨細胞腫とびまん型巨細胞腫
    　平滑筋肉腫
    　横紋筋肉腫
    　血管内皮腫と血管肉腫
    　悪性末梢神経鞘腫瘍
    　滑膜肉腫
    　類上皮肉腫
    　胞巣状軟部肉腫
    　明細胞肉腫
    　骨外性粘液型軟骨肉腫
    　未分化多形肉腫

    5章　病理検体の取り扱い

    6章　症例の実際
    　症例1　benign notochordal cell tumor
    　症例2　骨類上皮血管肉腫
    　症例3　phosphaturic mesenchymal tumor
    　症例4　軟部Pecoma
    　症例5　炎症性筋線維芽細胞性腫瘍
    　症例6　低悪性度線維粘液肉腫
    　症例7　軟部悪性ラブドイド腫瘍

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1章 病理診断の流れとポイント

P.2 掲載の参考文献
Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC Press ; 2013.
 
Weiss SW, Goldblum JR. eds. Enzinger & Weiss's Soft Tissue Tumors. Fifth ed. Mosby Inc ; 2008. p.129-174.
 
小田義直. 生検, 免疫組織化学染色と遺伝子診断. 大塚隆信ほか編. 骨軟部腫瘍 臨床画像病理. 東京 : 診断と治療社 ; 2011. p.62-9.
 

2章 診断のための基本知識

P.18 掲載の参考文献
Donald R, et al. Tumors and tumor-like lesions of bone. In : Donald R, et al. eds. Bone and Joint Imaging 3rd ed. Philadelphia : Saunders ; 2005. p.1109-98.
 
Theodore TM. Bone tumors and tumorlike conditions : analysis with conventional radiography. Radiology. 2008 ; 246 : 662-74.
 
Douis H, Saifuddin A.The imaging of cartilaginous bone tumours. I . Benign lesions. Skeletal Radiol. 2012 ; 41 : 1195-212.
PubMed
Douis H, Saifuddin A.The imaging of cartilaginous bone tumours. II . Chondrosarcoma. Skeletal Radiol. 2012 ; 42 : 611-26.
PubMed
Mark DM, et al. Imaging of osteochondroma : variants and complications with radiologicpathologic correlation. Radiographics. 2000 ; 20 : 1407-34.
 
Corey FC, et al. Giant cell tumor of bone : review, mimics, and new developments in treatment. Radiographics. 2013 ; 33 : 197-211.
 
Fee WC, et al. Radiologic diagnosis of osteoid osteoma : from simple to challenging findings. Radiographics. 2010 ; 30 : 737-49.
 
Donald JF, et al. Primary tumors of spine. Semin in musculoskel radiol. 2000 ; 4 : 299-320.
 
Geirnaerdt MJA, et al. Usefulness of Radiography in Differentiating Enchondroma from Central Grade I Chondrosarcoma. AJR. 1997 ; 169 : 1097-104.
 
G petur N, Michael K. Non-ossifying fibroma/benign fibrous histiocytoma of bone. In : Christopher DM Fletcher, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone 4th ed. Lyon : IARC ; 2013. p.302-4.
 
荒木力. MR画像の理解に必要な信号強度の基本. 日医師会誌. 2008 ; 137 : 945-50.
 
P.30 掲載の参考文献
青木隆敏ほか. 軟部組織疾患. 黒崎喜久編. 単純X線写真の読み方使い方. 東京 : 医学書院 ; 2013. p.371-7.
 
Amendola MA,et al. Myositis ossificans circumscripta : computed tomographic diagnosis. Radiology. 1983 ; 149 : 775-9.
PubMed
Kransdorf MJ, et al. Imaging of fatty tumors. distinction of lipoma and well-differentiated liposarcoma. Radiology. 2002 ; 224 : 99-104.
PubMed
Ohguri T, et al. Differential diagnosis of benign lipoma from well-differentiated liposarcoma on MRI : is comparison of their margins and internal characteristics useful? AJR. 2003 ; 180 : 1689-94.
PubMed
Jelinek JS, et al. Liposarcoma of the extremities : MR and CT findings in the histologic subtypes. Radiology. 1993 ; 186 : 455-9.
PubMed
Murphy MD, et al. Imaging of soft-tissue myxoma with emphasis on CT and MR and comparison of radiologic and pathologic findings. Radiology. 2002 ; 225 : 215-24.
 
Varma DGK, et al. MR imaging of extracranial nerve sheath tumors. J Comput Assist Tomogr. 1992 ; 16 : 448-53.
 
Burk P, et al. Meniscal and ganglion cysts of the knee : MR evaluation. AJR. 1988 ; 150 : 331-6.
 
Miller TT, et al. MR imaging of Baker cysts : Association with internal derangement effusion, and degenerative arthropathy. Radiology. 1996 ; 201 : 247-50.
PubMed
Aoki T, et al. The radiological findings in chronic expanding hematoma. Skeletal Radiol. 1999 ; 28 : 396-401.
PubMed
Quinn SF, et al. MR imaging in fibromatosis : results in 26 patients with pathologic correlation. AJR. 1991 ; 156 : 539-42.
PubMed
De Beuckeleer LH, et al. MR imaging of clear cell sarcoma (malignant melanoma of the soft parts) : a multicenter correlative MRI-pathology study of 21 cases and literature review. Skeletal Radiol. 2000 ; 29 : 187-95.
 
青木隆敏. 画像診断の進歩-どこまで病理診断に迫ってきているか : 軟部組織. 病理と臨床. 2007 ; 25 : 919-26.
 
P.40 掲載の参考文献
天児民和. 骨銀行の利用価値とその限界. 外科治療. 1959 ; 1 : 324.
 
冷凍ボーンバンクマニュアル. 日整外会誌. 2003 ; 77 (5) : 234-41.
 
整形外科移植に関するガイドライン. 日整外会誌. 2003 ; 77 (5) : 216-33.
 
Fletcher C D M, et al. WHO Classification of Tumours of Soft Tissue and Bone. Fourth Edi. Lyon : IARC ; 2013.
 
Biermann JS, et al. Bone cancer. National Comprehensive Cancer Network Bone Cancer Panel. J Natl Compr Canc Netw. 2010 ; 8 (6) : 688-712.
 
Iwamoto Y, et al. Multiinstitutional phase II study of neoadjuvant chemotherapy for osteosarcoma (NECO study) in Japan : NECO-93J and NECO-95J. J Orthop Sci. 2009.
PubMed
日本整形外科学会骨軟部腫瘍委員会編. 整形外科病理 悪性骨腫瘍取扱い規約. 第3版. 東京 : 金原出版 ; 2000.
 
Imai R, et al. Carbon ion radiotherapy for unresectable sacral chondromas. Clin Cancer Res. 2004 ; 10 : 5741-6.
 
P.52 掲載の参考文献
日本整形外科学会骨軟部腫瘍委員会編. 骨軟部肉腫切除縁評価法. 東京 : 金原出版 ; 1989.
 
Adjuvant chemotherapy for localised resectable soft-tissue sarcoma of adults : metaanalysis of individual data. Sarcoma Meta-analysis Collaboration. Lancet. 1997 ; 350 : 1647-54.
PubMed
日本整形外科学会骨軟部腫瘍委員会編. 整形外科病理悪性軟部腫瘍取扱い規約 第3版. 東京 : 金原出版 ; 2002.
 
Breneman JC, et al. Prognostic factors and clinical outcomes in children and adolescents with metastatic rhabdomyosarcoma-a report from the Intergroup Rhabdomyosarcoma Study IV. Journal of Clinical Oncology : official journal of the American Society of Clinical Oncology. 2003 ; 21 : 78-84.
PubMed
Grier HE, et al. Addition of ifosfamide and etoposide to standard chemotherapy for Ewing's sarcoma and primitive neuroectodermal tumor of bone. The New England Journal of Medicine. 2003 ; 348 : 694-701.
PubMed
鎌田正. 悪性軟部腫瘍の放射線療法. 吉川秀樹編. 最新整形外科学大系 20 骨軟部腫瘍および関連疾患. 東京 : 中山書店 ; 2007. p.158-60.
 
Weiss SW, Goldblum JR. Enzinger & Wieiss's Soft Tissue Tumors Fifth Edition. Mosby Elsevier ; 2008.
 
Chung PW, et al. Radiosensitivity translates into excellent local control in extremity myxoid liposarcoma : a comparison with other soft tissue sarcomas. Cancer. 2009 ; 115 : 3254-61.
PubMed
Tanaka K, et al. Preoperative and postoperative chemotherapy with ifosfamide and adriamycin for adult high-grade soft-tissue sarcomas in the extremities : Japan Clinical Oncology Group Study JCOG0304. Japanese Journal of Clinical Oncology. 2009 ; 39 : 271-3.
 
Sobin LH, et al. eds. UICC (International Union Against Cancer) TNM Classification of Malignant Tumors Seventh Edition. Wiley-Blackwell ; 2009.
 
日本小児がん学会編. 小児がん診療ガイドライン 2011年度版. 東京 : 金原出版 ; 2011.
 
Malempati S, Hawkins DS. Rhabdomyosarcoma : review of the Children's Oncology Group (COG) Soft-Tissue Sarcoma Committee experience and rationale for current COG studies. Pediatric blood & cancer. 2012 ; 59 : 5-10.
 
日本整形外科学会診療ガイドライン委員会, 軟部腫瘍診療ガイドライン策定委員会編. 軟部腫瘍診療ガイドライン 2012 改訂第2版. 東京 : 南江堂 ; 2012.
 
Fletcher, et al. "WHO Classification of Tumors of Soft Tissue and Bone Fourth Edition", IARC. 2013.
 
P.64 掲載の参考文献
Hasegawa T. Histological grading and MIB-1 labeling index of soft-tissue sarcomas. Pathol Int. 2007 ; 57 : 121-5.
PubMed
Edge SB, et al. AJCC Cancer Staging Manual. 7th ed. New York : Springer ; 2010, p.291-8.
 
Guillou L, et al. Comparative study of the National Cancer Institute and French Federation of Cancer Centers Sarcoma Group grading systems in a population of 410 adult patients with soft tissue sarcoma. J Clin Oncol. 1997 ; 15 : 350-62.
 
Evans HL, et al. Prognostic factors in chondrosarcoma of bone. A clinicopathologic analysis with emphasis on histologic grading. Cancer. 1977 ; 40 : 818-31.
 

3章 骨腫瘍の概要と鑑別診断

P.72 掲載の参考文献
野島孝之. 第10章 骨関節. 松原修ほか編. カラーアトラス 病理組織の見方と鑑別診断. 第5版. 東京 : 医歯薬出版 ; 2007. p. 409-38.
 
de Andrea CE, et al. Osteoblastoma. In : Flecher CDM, et al. eds. WHO classification of tumours of soft tissue and bone. Lyon : IARC ; 2013. p. 279-80.
 
Garcia RA, et al. Benign bone tumors-recent development. Semin Diagn Pathol. 2011 ; 28 : 73-85.
PubMed
Horvai A, Klein M. Osteoid osteoma. In : Flecher CDM, et al. eds. WHO classification of tumours of soft tissue and bone. Lyon : IARC ; 2013. p. 277- 8.
 
McHugh JB, et al. Sino-orbital osteoma : A clinicopathologic study of 45 surgically treated cases with emphasis on tumor with osteoblastoma-like features. Arch Pathol Lab Med. 2009 ; 133 : 1587-93.
PubMed
Nielsen GP, Rosenberg AE. Bone-forming tumors. In : Folpe AL, Inwards CY, eds. Bone and soft tissue pathology. Philadelphia : Saunders ; 2010. p. 309-29.
 
Unni KK, et al. Bone-forming lesions. In : Squazzo KA, et al. eds. AFIP atlas of tumor pathology series 4. Tumor of the bones and joints. Washington, DC : American Registry of Pathology ; 2005. p. 119-92.
 
P.78 掲載の参考文献
Fletcher CDM, et al. ed. World Health Organization classification of tumors. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC Press ; 2013.
 
Unni KK, Inwards CY. Dahlin's Bone Tumors sixth edition. Lippincott : Williams & Wilkins ; 2009.
 
Greenspan A, et al. Differential Diagnosis in Orthopaedic Oncology second ed. Lippincott : Williams & Wilkins ; 2006.
 
Yoshida A, et al. Immunohistochemical analysis of MDM2 and CDK4 distinguishes lowgrade osteosarcoma from benign mimics. Mod Pathol. 2010.
PubMed
P.91 掲載の参考文献
骨腫瘍の病理. 悪性骨腫瘍取扱い規約. 第3版. 日本整形外科学会, 骨軟部腫瘍委員会編. 東京 : 金原出版 ; 2000. p.99-102.
 
石田剛. 骨表面骨肉腫. 骨腫瘍の病理. 東京 : 文光堂 ; 2012. p.97-114.
 
Okada K, et al. Parosteal osteosarcoma. A clinicopathological study. J Bone Joint Surg Am. 1994 ; 76 : 366-78.
PubMed
Bertoni F, et al. Dedifferentiated parosteal osteosarcoma : the experience of the Rizzoli Institute. Cancer. 2005 ; 103 (11) : 2373-82.
PubMed
Hoshi M, et al. Oncogenic outcome of parosteal osteosarcoma. Int J Clin Oncol. 2006 ; 11 : 120-6.
 
Duhamel LA, et al. Frequency of Mouse Double Minute 2 (MDM2) and Mouse Double Minute 4 (MDM4) amplification in parosteal and conventional osteosarcoma subtypes. Histopathology. 2012 ; 60 : 357-9.
PubMed
Unni KK, et al. Osteosarcomas of the Surface of Bone. In : Unni KK, et al. eds. Tumors of the Bones and Joints, AFIP Atlas of Tumor Pathology, 4th Series. Washington, D. C. : American Registry of Pathology ; 2005. p.171-84.
 
Rose PS, et al. Periosteal osteosarcoma : long-term outcome and risk of late recurrence. Clin Orthop Relat Res. 2006 ; 453 : 314-7.
PubMed
Hoshi M, et al. Three cases with periosteal osteosarcoma arising from the femur. J Orthop Sci. 2006 ; 11 : 224-8.
PubMed
Cesari M, et al. Periosteal osteosarcoma : a single-institution experience. Cancer. 2011 ; 117 : 1731-5.
PubMed
Okada K, et al. High grade surface osteosarcoma : a clinicopathologic study of 46 cases. Cancer. 1999 ; 85 : 1044-54.
PubMed
Hoshi M, et al. Report of four cases with high-grade surface osteosarcoma. Jpn J Clin Oncol. 2006 ; 36 : 180-4.
PubMed
Staals EL, et al. High-grade surface osteosarcoma : a review of 25 cases from the Rizzoli Institute. Cancer. 2008 ; 112 : 1592-9.
PubMed
P.103 掲載の参考文献
Unni KK, Inwards CY. Dahlin's bone tumors : general aspects and data on 10,165 cases. 6th ed. Philadelphia : Lippincott Williams&Wilkins ; 2010.
 
Fletcher CDM, et al, eds. WHO classification of tumours of soft tissue and bone. Lyon : IARC ; 2013.
 
Unni KK, et al. In : Silverberg SG, Sobin LH, eds. AFIP atlas of tumor pathology, 4th series. Tumors of the bones and joints. Silver Spring : ARP PRESS ; 2005.
 
日本整形外科学会, 骨軟部腫瘍委員会編. 整形外科病理 悪性骨腫瘍取扱い規約. 第3版. 東京 : 金原出版 ; 2000. p. 84-158.
 
Amary MF, et al. Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2. Nat Genet. 2011 ; 43 : 1262-5.
PubMed
Jones KB, et al. A mouse model of osteochondromagenesis from clonal inactivation of Ext1 in chondrocytes. PNAS. 2010 ; 107 : 2054-9.
PubMed
P.133 掲載の参考文献
Romeo S, et al. Malignant fibrous histiocytoma and fibrosarcoma of bone : a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches. Virchows Arch. 2012 ; 461 : 561-70.
 
Fletcher CDM, et al. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013.
 
Nielsen GP, et al. Diagnostic Pathology. Bone. AMIRSYS ; 2013.
 
石田剛. 骨腫瘍の病理. 東京 : 文光堂 ; 2012.
 
Dorfman HD, Czerniak B. Bone tumors. Philadelphia : Mosby ; 1998.
 
Unni KK, Inward C. Dahlin's Bone Tumors. Philadelphia : Wolters Kluwer/Lippincott Williams & Wilkins ; 2010.
 
P.143 掲載の参考文献
de Alva E, et al. Ewing sarcoma. In : Fletcher CDM, et al, eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013. p.305-9.
 
Folpe AL, et al. Immunohistochemical detection of FLI-1 protein expression : a study of 132 roundcell tumors with emphasis on CD99-positive mimics of Ewing's sarcoma/primitiveneuroectodermal tumor. Am J Surg Pathol. 2000 ; 24 (12) : 1657-62.
 
Fletcher CDM, et al. Undifferentiated/unclassified sarcomas. In : Fletcher CDM, et al, eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013. p.236-8.
 
Kawamura-Saito M, et al. Fusion between CIC and DUX4 up-regulates PEA3 family genes in Ewing-like sarcomas with t (4 ; 19) (q35 ; q13) translocation. Hum Mol Genet. 2006 ; 15 (13) : 2125-37.
 
Pierron G, et al. A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion. Nat Genet. 2012 ; 44 (4) : 461-6.
PubMed
Wang L, et al. Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymalchondrosarcoma based on a genome-wide screen of exon-level expression data.Genes Chromosomes Cancer. 2012 ; 51 (2) : 127-39.
PubMed
Bishop JA, Westra WH . NUT midline carcinomas of the sinonasal tract. Am J Surg Pathol. 2012 ; 36 (8) : 1216-21.
PubMed
P.156 掲載の参考文献
Lorsbach R, Kluin PM. Plasma cell myeloma, and Solitary plasmacytoma of bone. In : Fletcher CDM, et al. ed. WHO Classification of Tumours of Soft Tissue and Bone. 4th ed. Lyon : IARC Press ; 2013. p.312-5.
 
Hogendoorn PCW, Kluin PM. Primary non-Hodgkin Lymphoma of Bone. In : Fletcher CDM, et al. ed. WHO classification of Tumours of Soft Tissue and Bone. 4th ed. Lyon : IARC Press ; 2013. p.316-8.
 
Unni KK, Inwards CY. Malignant lymphoma of bone. In : Dahlin's Bone Tumors, 6th ed. Lippincott : Williams & Wilkins ; 2010. p.201-10.
 
Nielsen GP, Rosenberg AE. Primary lymphoma. In : Nielsen GP, Rosenberg AE, eds. Diagnostic Pathology, Bone. Amirsys 2013 ; 12 p.8-15.
 
McKenna RW, et al. Plasma cell neoplasms. In : Swerdlow SH, et al. eds. WHO Classification of Tumours of Haematologic and Lymphoid Tissues. Lyon : IARC press ; 2008. p.200-13.
 
坂井晃. 多発性骨髄腫の病気分類と予後因子. 木崎昌弘編. 多発性骨髄腫治療マニュアル. 東京 ; 南江堂 ; 2012. p.75-80.
 
Martinez A, et al. Primary bone marrow lymphoma : an uncommon extranodal presentation of aggressive non-hodgkin lymphomas. Am J Surg Pathol. 2012 ; 36 (2) : 296-304.
PubMed
P.165 掲載の参考文献
Franagan AM, Yamaguchi T. Chordoma. WHO Classification of Tumors of Soft Tissue and Bone, 4th ed. In : Fletcher CMD, et al. eds. Lyon : IARC Press ; 328-9.
 
McMaster ML, et al. Chordoma : incidence and survival patterns in the United States, 1973-1995. Cancer Causes Control. 2001 ; 12 : 1-11.
PubMed
Mukherjee D, et al. Survival of patients with malignant primary osseous spinal neoplasms : results from the Surveillance, Epidemiology, and End Results (SEER) database from 1973 to 2003. J Neurosurge spine. 2011 ; 14 : 143-50.
 
日本整形外科学会骨軟部腫瘍委員会編, 国立がん研究センター. 全国骨腫瘍登録一覧表. 2010. p.26-7.
 
Rutherfoord GS, Davies AG. Chordomas-ultrastructure and immunohitochemistory : a report based on the examination of six cases. Histopathology. 1987 : 11 ; 775-87.
PubMed
P.178 掲載の参考文献
World Health Organization Classification of Tumours of Soft Tissue and Bone. Lyon : IARC Press ; 2013. p.347- 49, 319-20.
 
Dorfman HD, Czerniak. Bone tumors. St Louis : Mosby ; 1998. p.855-67, 598-604.
 
Leithner A, et al. Aneurysmal bone cyst. A population based epidemiologic study and literature review. Clin Orthop Relat Res. 1999 ; 363 : 176-9.
PubMed
Panoutsakopoulos G, et al. Recurrent t (16 ; 17) (q22 ; p13) in aneurysmal bone cysts. Genes Chromosomes Cancer. 1999 ; 26 : 265-6.
PubMed
Lorenzo JC, Dorfman HD. Giant-cell reparative granuloma of short tubular bones of the hands and feet. Am J Surg Pathol. 1980 ; 4 : 551- 63.
 
Murphey MD, Nomikos GC, Flemming DJ, et al. From the archives of AFIP. Imaging of giant cell tumor and giant cell reparative granuloma of bone : radiologic-pathologic correlation. Radiographics. 200 ; 21 : 1283-309.
 
Buresh CJ, et al. t (X ; 4) (q22 ; q31.3) in giant cell reparative granuloma. Cancer Genet Cytogenet. 1999 ; 115 : 80-1.
PubMed
Pan Z, et al. A novel t (6 ; 13) (q15 ; q34) translocation in a giant cell reparative granuloma (solid aneurysmal bone cyst). Hum Pathol. 2012 ; 43 : 952-7.
 
P.184 掲載の参考文献
Fletcher CDM, et al. ed. World Health Organization classification of tumors. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC Press ; 2013.
 
Unni KK, Inwards CY. Dahlin's Bone Tumors, 6th ed. Philadelphia : Lippincott Williams & Wilkins ; 2009.
 
Idowu BD, et al. A sensitive mutation-specific screening technique for GNAS1 mutations in cases of fibrous dysplasia : the first report of a codon 227 mutation in bone. Histopathology. 2007 : 50 : 691-704.
PubMed
Khanna M, et al. Osteofibrous dysplasia, osteofibrous dysplasia-like adamantinoma and adamantinoma : correlation of radiological imaging features with surgical histology and assessment of the use of radiology in contributing to needle biopsy diagnosis. Skeletal Radiol. 2008 ; 37 : 1077-84.
PubMed

4章 軟部腫瘍の概要と鑑別診断

P.204 掲載の参考文献
Rosenberg AE. Pseudosarcomas of soft tissue. Arch Pathol Lab Med. 2008 ; 132 : 579-86.
PubMed
Krandorf MJ, Meis JM. From the archives of the AFIP. Extraskeletal osseous and cartilaginous tumors of the extremities. Radiographics. 1993 ; 13 : 853-84.
 
Erickson-Johnson MR, et al. Nodular fasciitis : a novel model of transient neoplasia induced by MYH9-USP6 gene fusion. Lab Invest. 2011 ; 91 : 1427-33.
PubMed
Spjut HJ, Dorfman HD. Florid reactive periostitis of the tubular bones of the hands and feet. Am J Surg Pathol. 1981 ; 5 : 423-33.
PubMed
Weiss SW, Goldblum JR. Benign fibroblastic/myofibroblastic proliferations. In : Weiss SW, Goldblum JR, eds. Soft Tissue Tumors, 5th ed. Amsterdam : Elsevier ; 2008. p.175-226.
 
Lazar A, et al. Nodular fasciitis. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. 4th ed. Lyon : IARC press ; 2013. p. 46-7.
 
P.221 掲載の参考文献
Saito T, et al. beta-catenin nuclear expression correlates with cyclin D1 overexpression in sporadic desmoid tumours. J Pathol. 2001 ; 195 : 222-8.
PubMed
Lazar AJ, et al. Specific mutations in the beta-catenin gene (CTNNB1) correlate with local recurrence in sporadic desmoid tumors. Am J Pathol. 2008 ; 173 : 1518-27.
PubMed
Yamamoto H, et al. Kit-negative gastrointestinal stromal tumor of the abdominal soft tissue : a clinicopathologic and genetic study of 10 cases. Am J Surg Pathol. 2011 ; 35 : 1287-95.
 
Hauben EI, et al. Desmoplastic fibroma of bone : an immunohistochemical study including b-catenin expression and mutational analysis for b-catenin. Human Pathol. 2005 ; 36 : 1025-30.
 
Erickson-Johnson MR, et al. Nodular fasciitis : a novel model of transient neoplasia induced by MYH9-USP6 gene fusion. Lab Invest. 2011 ; 91 : 1427-33.
PubMed
P.229 掲載の参考文献
Mentzel T, et al. Dermatofibrosarcoma protuberans. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013. p. 77-9.
 
Mark D, et al. Radiologic evaluation of soft tissue tumors. In : Weiss SW, Goldblum JR, eds. Enzinger and Weiss Soft Tissue Tumors 5th ed. Philadelphia : Mosby ; 2008. p. 33-71.
 
Kesserwan C, et al. Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase-deficient severe combines immune deficiency. J Allergy Clin Immunol. 2012 ; 129 : 762-9.
PubMed
Reimann JDR, Fletcher CDM. Myxoid dermatofibrosarcoma protuberans : A rare variant analyzed in a series of 23 cases. Am J Surg Pathol. 2007 ; 31 : 1371-7.
 
Calonje E, Fletcher CDM. Myoid differentiation in dermatofibrosarcoma protuberans and its fibrosarcomatous variant : clinicopathological analysis of 5 cases. J Cutan Pathol. 1996 ; 23 : 30-6.
 
Davis DA, Sanchez RL. Atrophic and plaquelike dermatofibrosarcoma protuberans. Am J Dermatopathol. 1998 ; 20 : 498-501.
PubMed
Kutzner H, et al. Plaque-like CD34-positive dermal fibroma ("medallion-like dermal dendrocyte hamartoma") : clinicopathologic, immunohistochemical, and molecular analysis of 5 cases emphasizing its distinction from superficial, plaque-like dermatofibrosarcoma protuberans. Am J Surg Pathol. 2010 ; 34 : 190-201.
PubMed
Abbott JJ, et al. The prognostic significance of fibrosarcomatous transformation dermatofibrosarcoma protuberans. Am J Surg Pathol. 2006 ; 30 : 436-43.
PubMed
Llombart B, et al. Dermatofibrosarcoma protuberans : a comprehensive review and update on diagnosis and management. Semin Diag Pathol. 2013 ; 30 : 13-28.
 
Heinrich MC, et al. Phase II , open-label study evaluating the activity of imatinib in treating life-threatening malignancies known to be associated with imatinib-sensitive tyrosine kinases. Clin Cancer Res. 2008 ; 14 : 2717-25.
PubMed
P.237 掲載の参考文献
Fletcher CDM, et al. Extrapleural solitary fibrous tumor. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013. p. 80-2.
 
Mark D, et al. Radiologic evaluation of soft tissue tumors. In : Weiss SW, Goldblum JR, eds. Enzinger and Weiss Soft Tissue Tumors 5th ed. Philadelphia : Mosby ; 2008. p. 33-71.
 
Hasegawa T, et al. Extrathoracic solitary fibrous tumors : their histological variability and potentially aggressive behavior. Hum Pathol. 1999 ; 30 : 1464-73.
PubMed
de Saint Aubain Somerhausen N, et al. Myxoid solitary fibrous tumor : a study of seven cases with emphasis on differential diagnosis. Mod Pathol. 1999 ; 12 : 463-71.
PubMed
Guillou L, et al. Lipomatous hemangiopericytoma : a fat-containing variant of solitary fibrous tumor? Clinicopathologic, immunohistochemical, and ultrastructural analysis of a series in favor of a unifying concept. Hum Pathol. 2000 ; 31 : 1108-15.
PubMed
Mosquera JM, Fletcher CDM. Expading the spectrum of malignant progression in solitary fibrous tumors : a study of 8 cases with a discrete anaplastic component-is this dedifferentiated SFT? Am J Surg Pathol. 2009 ; 33 (9) : 1314-21.
PubMed
Chmielecki J, et al. Whole-exome sequencing indentifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors. Nature Genetics. 2013 ; 45 : 131-2.
 
Marino-Enriquez A, Fletcher CDM. Angiofibroma of soft tissue : clinicopathologic characterization of a distinctive benign fibrovascular neoplasm in a series of 37 cases. Am J Surg Pathol. 2012 ; 36 : 500-8.
 
Edgar MA, et al. Soft tissue angiofibroma : report of 2 cases of a recently described tumor. Hum Pathol. 2013 ; 44 : 438-41.
PubMed
Fletcher CDM, et al. Cellular angiofibroma. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013. p. 65-6.
 
McMenamin M, Debiec-Rychter M. Mammary-type myofibroblastoma. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013. p. 61-2.
 
Miettinen MM, Mandahl N. Spindle cell/pleomorphic lipoma. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013. p. 29-30.
 
P.245 掲載の参考文献
Mentzel T, et al. Myxofibrosarcoma. Clinicopathologic analysis of 75 cases with emphasis on the low-grade variant. Am J Surg Pathol. 1996 ; 20 : 391- 405.
 
Nascimento AF, et al. Epithelioid variant of myxofibrosarcoma : expanding the clinicomorphologic spectrum of myxofibrosarcoma in a series of 17 cases. Am J Surg Pathol. 2007 ; 31 : 99-105.
 
Oda Y, et al. Low-grade fibromyxoid sarcoma versus low-grade myxofibrosarcoma in the extremities and trunk. A comparison of clinicopathological and immunohistochemical features. Histopathology. 2004 ; 45 : 29-38.
 
Hisaoka M, et al. Retroperitoneal liposarcoma with combined well-differentiated and myxoid malignant fibrous histiocytoma-like myxoid areas. Am J Surg Pathol. 1999 ; 23 : 1480-92.
PubMed
Huang HY, et al. Distant metastasis in retroperitoneal dedifferentiated liposarcoma is rare and rapidly fatal : a clinicopathological study with emphasis on the low-grade myxofibrosarcoma-like pattern as an early sign of dedifferentiation. Mod Pathol. 2005 ; 18 : 976-84.
 
Antonescu CR, et al. Consistent t (1 ; 10) with rearrangements of TGFBR3 and MGEA5 in both myxoinflammatory fibroblastic sarcoma and hemosiderotic fibrolipomatous tumor. Genes Chromosomes Cancer. 2011 ; 50 : 757- 64.
 
Folpe AL, et al. Low-grade fibromyxoid sarcoma and hyalinizing spindle cell tumor with giant rosettes : a clinicopathologic study of 73 cases supporting their identity and assessing the impact of high-grade areas. Am J Surg Pathol. 2000 ; 24 : 1353-60.
PubMed
久岡正典. 粘液状腫瘍. 小田義直, 長谷川匡編. 腫瘍鑑別診断アトラス 軟部腫瘍. 東京 : 文光堂 ; 2011. p.183-90.
 
P.253 掲載の参考文献
Weiss SW, Goldblum JR, eds. Enzinger and Weiss's. Soft tissue tumors. 5th ed. Philadelphia : Mosby Inc ; 2008. p.769-88.
 
Fletcher CD, eds. WHO Classification of Tumors of Soft Tissue and Bone, 4th ed. IARC. Lyon : 2013. p.100-3.
 
P.260 掲載の参考文献
Farshid G, et al. Leiomyosarcoma of somatic soft tissues : a tumor of vascular origin with multivariate analysis of outcome in 42 cases. Am J Surg Pathol. 2002 ; 26 : 14-24.
PubMed
Weiss SW, Goldblum JR. Leiomyosarcoma. In : Weiss SW, Goldblum JR, eds. Soft Tissue Tumors, 5th ed. Amsterdam : Elsevier ; 2008.
 
Abraham JA, et al. Outcomes and prognostic factors for a consecutive case series of 115 patients with somatic leiomyosarcoma. J Bone Joint Surg Am. 2012 ; 94 : 736-44.
PubMed
Lazar A, et al. Leiomyosarcoma. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone, 4th ed. Lyon : IARC press ; 2013. p.111-3.
 
P.268 掲載の参考文献
Hostein I, et al. Rhabdomyosarcoma : value of myogenin expression analysis and molecular testing in diagnosing the alveolar subtype. An analysis of 109 paraffin-embedded specimens. Cancer. 2004 ; 101 : 2817-24.
PubMed
Bahrami A, et al. Aberrant expression of epithelial and neuroendocrine markers in alveolar rhabdomyosarcoma : a potentially serious diagnostic pitfall. Mod Pathol. 2008 ; 21 : 795-806.
PubMed
Davicioni E, et al. Molecular classification of rhabdomyosarcoma-genotypic and phenotypic determinants of diagnosis. A report from the children's oncology group. Am J Pathol. 174 ; 550-64.
 
Skapek SX, et al. PAX-FOXO1 fusion status drives unfavorable outcome for children with rhabdomyosarcoma : a children's oncology group report. Pediatr Blood Cancer. 2013 ; in press.
 
Fletcher CDM, et al. eds. World Health Organization Classification Tumours WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC Press, 2013.
 
P.280 掲載の参考文献
Fletcher CDM, et al. WHO Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. Lyon : IRAC Press ; 2013.
 
Fukunaga M, et al. Kaposiform hemangioendothelioma associated with Kasabach-Merritt syndrome. Histopathol. 1996 : 28 ; 281-4.
 
Fukunaga M, et al. Retiform hemangioendothelioma. Virchows Arch. 1996 ; 428 : 301-4.
PubMed
Fanburg-Smith JC, et al. Papillary intralymphatic angioendothelioma (PILA) ; a report of twelve cases of a distinctive vascular tumor with phenotypic features of lymphatic vessels. Am J Surg Pathol. 1999 ; 23 : 1004-10.
 
Fukunaga M, et al. Composite hemangioendothelioma : report of 5 cases including one with associated Maffucci syndrome. Am J Surg Pathol. 2007 ; 31 : 1567-72.
PubMed
Honick JL, Fletcher CD. Pseudomyogenic hemangioendothelioma : a distinctive oftern multicentric tumor with indolent behavior. Am J Surg Pathol. 2011 ; 35 : 190-201.
 
Billings SD, et al. Epithelioid sarcoma-like hemangioendothelioma. Am J Surg Pathol. 2003 ; 27 : 148-57.
 
Fukunaga M. Expression of D2-40 in lymphatic endothelium of normal tissues and in vascular tumours. Histopathol. 2005 ; 46 : 396-402.
 
Mentzel T, et al. Epithelioid hemangioendothelioma of the skin and soft tissues ; clinicopathologic and immunohistochemical studies of 30 cases. Am J Surg Pathol. 1997 ; 21 : 363-74.
PubMed
Fletcher CDM, et al. Epithelioid angiosarcoma of deep soft tissue ; distinctive tumor readily mistaken for an epithelial neoplasm. Am J Surg Pathol. 1991 ; 15 : 915-24.
 
福永真治. 類上皮血管内皮腫. 長谷川匡, 小田義直編. 腫瘍病理鑑別診断アトラス軟部腫瘍. 東京 : 文光堂 ; 2011. p. 89-94.
 
Brenn T, Fletcher CDM. Radiation-associated cutaneous atypical vascular lesions and angiosarcoma. Clinicopathologic analysis of 42 cases. Am J Surg Pathol. 2005 ; 29 : 983-96.
PubMed
P.296 掲載の参考文献
Nielsen GP, et al. Malignant peripheral nerve sheath tumour. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone, 4th eds. Lyon : International Agency for Research on Cancer ; 2013. p. 187-9.
 
Miettinen M. Nerve sheath tumors. In : Miettinen M, ed. Modern Soft Tissue Pathology. Cambridge : Cambridge University Press ; 2010. p. 660-723.
 
Fanburg-Smith JC. Nerve sheath and neuroectodermal tumors. In : Folpe AL, Inwards CY, eds. Bone and Soft Tissue Pathology. Philadelphia : Saunders ; 2010. p. 193-238.
 
Weiss SW, Goldblum JR. Malignant tumors of the peripheral nerves. In : Enzinger and Weiss's Soft Tissue Tumors, 5th ed. Mosby ; 2008. p. 903-44.
 
Scheithauer BW, et al. Primary malignant tumors of peripheral nerve. In : Atlas of Tumor Pathology, 3rd series, fascicle 24. Tumors of the Peripheral Nervous System. Washington, D. C. : Armed Forces Institute of Pathology ; 1999. p. 303-72.
 
Scheithauer BW, et al. Malignant peripheral nerve sheath tumour (MPNST). In : Louis DN, eds. WHO Classification of Tumours of the Central Nervous System, 4th ed. Lyon : International Agency for Research on Cancer ; 2007. p. 160-2.
 
P.307 掲載の参考文献
Suurmeijpr AJH, et al. Synovial sarcoma. In : Fletcher CDM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC ; 2013. p.155-6.
 
Miettinen M, Virtanen I. Synovial sarcoma-a misnomer. Am J Pathol. 1984 ; 117 : 18-25.
PubMed
dos Santos NR, et al. Molecular mechanisms underlying human synovial sarcoma development. Genes Chromosomes Cancer. 2001 ; 30 : 1-14.
PubMed
Sonobe H, et al. Establishment and characterization of a new human synovial sarcoma cell line, HS-SY-II. Lab lnvest. 1992 ; 67 : 498-505.
PubMed
Sultan I, et al. Comparing children and adults with synovial sarcoma in the Surveillance, Epidermiology, and End Results program, 1983 to 2005 : an analysis of 1286 patients. Cancer. 2009 ; 115 : 3537-47.
 
Pelmus, et al. Monophasic fibrous and poorly differentiated synovial sarcoma : immunohistochemical reassessment of 60 t (X ; 18) (SYT-SSX)-positive cases. Am J Surg Pathol. 2002 : 26 : 1434-40.
PubMed
元井亨, 熊谷有紗. 滑膜肉腫. 長谷川匡, 小田義直編. 軟部腫瘍, 腫瘍病理鑑別診断アトラス. 東京 : 文光堂 ; 2011. p.116-25.
 
P.316 掲載の参考文献
Billings SD, et al. Epithelioid sarcoma-like hemangioendothelioma. Am J Surg Pathol. 2003 ; 27 : 48-57.
PubMed
Guillou L, et al. "Proximal-type" epithelioid sarcoma, a distinctive aggressive neoplasm showing rhabdoid features. Clinicopathologic, immunohistochemical, and ultrastructural study of a series. Am J Surg Pathol. 1997 ; 21 : 130-46.
PubMed
Prat J, et al. Epithelioid sarcoma : an analysis of 22 cases indicating the prognostic significance of vascular invasion and regional lymph node metastasis. Cancer. 1978 ; 4 : 1472-87.
PubMed
Kohashi K, et al. SMARCB1/INI1 protein expression in round cell soft tissue sarcomas associated with chromosomal translocations involving EWS : a special reference to SMARCB1/INI1 negative variant extraskeletal myxoid chondrosarcoma. Am J Surg Pathol. 2008 ; 32 : 1168-74.
PubMed
Kohashi K, et al. Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma : a useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor. Hum Pathol. 2009 ; 40 : 349-55.
PubMed
Hornick JL, Fletcher CD. Pseudomyogenic hemangioendothelioma : a distinctive, often multicentric tumor with indolent behavior. Am J Surg Pathol. 2011 ; 35 : 190-201.
PubMed
Mirra JM, et al. The fibroma-like variant of epithelioid sarcoma. A fibrohistiocytic/myoid cell lesion often confused with benign and malignant spindle cell tumors. Cancer. 1992 ; 69 : 1382-95.
PubMed
Spillane AJ, et al. Epithelioid sarcoma : the clinicopathological complexities of this rare soft tissue sarcoma. Ann Surg Oncol. 2000 ; 7 : 218-25.
PubMed
P.329 掲載の参考文献
Weiss SW, Goldblum JR. Clear cell sarcoma of tendon and aponeurosis. In : Enzinger & Weiss's Soft tissue tumors, Fifth ed. Philadelphia : Mosby-Elsevier ; 2008. p.926-34.
 
Antonescu CR. Clear cell sarcoma of soft tissue. In : Fletcher DM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Geneva : World Health Organization ; 2013. p.221-2.
 
P.335 掲載の参考文献
Hisaoka M, et al. Microtubule-associated protein-2 and class III beta-tubulin are expressed in extraskeletal myxoid chondrosarcoma. Mod Pathol. 2003 ; 16 : 453-9.
PubMed
Lucas DR, et al. High-grade extraskeletal myxoid chondrosarcoma : a high-grade epithelioid malignancy. Histopathology. 1999 ; 35 : 201-8.
PubMed
Meis-Kindblom JM, et al. Extraskeletal myxoid chondrosarcoma : a reappraisal of its morphologic spectrum and prognostic factors based on 117 cases. Am J Surg Pathol. 1999 ; 23 : 636-50.
PubMed
Okamoto S, et al. Extraskeletal myxoid chondrosarcoma : a clinicopathologic, immunohistochemical, and molecular analysis of 18 cases. Hum Pathol. 2001 ; 32 : 1116-24.
PubMed
Oliveira AM, et al. Extraskeletal myxoid chondrosarcoma : a clinicopathologic, immunohistochemical, and ploidy analysis of 23 cases. Mod Pathol. 2000 ; 13 : 900-8.
PubMed
Stout AP, Verner EW. Chondrosarcoma of the extraskeletal soft tissues. Cancer. 1953 ; 6 : 581-90.
PubMed
Weiss SW. Ultrastructure of the so-called "chordoid sarcoma". Evidence supporting cartilagenous differentiation. Cancer. 1976 ; 37 : 300-6.
PubMed

5章 病理検体の取り扱い

P.356 掲載の参考文献
日本整形外科学会骨軟部腫瘍委員会編. 骨軟部肉腫切除縁評価法. 東京 : 金原出版 ; 1989.
 
Kawaguchi N, et al. The concept of curative margin in surgery for bone and soft tissue sarcoma. Clin Orthop. 2004 ; 419 : 165-72.
 
松本誠一ほか. 骨軟部肉腫の手術療法. 癌と化学療法. 2004 ; 31 : 1314-8.
Medical*Online
蛭田啓之ほか. 浸潤性発育を示す低悪性軟部肉腫の組織学的検討, 高悪性例との対比および切除縁との関連について. 日整会誌. 2007 ; 81 : S722.
Medical*Online
橋本洋. 軟部腫瘍の生検ならびに切除材料の取り扱いと診断へのアプローチ. 病理と臨床. 1999 ; 17 : 881-5.
 
野島孝之ほか. 骨腫瘍の生検ならびに切除材料の取り扱いと診断へのアプローチ. 病理と臨床. 1999 ; 17 : 1019-22.
Medical*Online
蛭田啓之ほか. 骨肉腫の術前化学療法組織学的効果判定と問題点. 日整会誌. 2010 ; 84 : 1120-125.
Medical*Online
蛭田啓之ほか. VI. 軟部肉腫の組織学的治療効果判定と切除縁評価. 長谷川匡ほか編. 腫瘍病理鑑別診断アトラス, 軟部腫瘍. 東京 : 文光堂 ; 2011. p.246-54.
 
石田剛. V. 骨腫瘍へのアプローチと検索方法. 骨腫瘍の病理. 東京 : 文光堂 ; 2012. p.27-33.
 
The 25th forum of the surgical society for musculoskeletal sarcoma, 抄録 ; 2013 : 3-4, 2013.
 
阿江啓介ほか. 切除縁評価法-バリア概念の検証-. 日整会誌. 2013 ; 87 : S1142.
Medical*Online

6章 症例の実際

P.366 掲載の参考文献
山口岳彦. 良性脊索細胞腫. 脊椎脊髄ジャーナル. 2010 ; 23 : 455-9.
 
Yamaguchi T, et al. Distinguishing benign notochordal cell tumor from vertebral chordoma. Skeletal Radiol. 2008 ; 37 : 291-9.
PubMed
Yamaguchi T, et al. Intraosseous benign notochordal cell tumors-overlooked precursors of classic chordomas? Histopathology. 2004 ; 44 : 597- 602.
 
Nishiguchi T, et al. Lumbar vertebral chordoma arising from an intraosseous benign notochordal cell tumour : radiological findings and histopathological description with a good clinical outcome. Br J Radiol. 2010 ; 83 : e49-53.
PubMed
Lee YD, et al. Array comparative genomic hybridization analysis show that a conventioanl chordoma and an adjacent benign notochordal tumor lack lineage relationship. Fourth International Chordoma Research Workshop, Boston, March 21-22, 2013.
 
Fletcher CDM, et al. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC Press ; 2013.
 
Nielsen GP, et al. Diagnostic Pathology. Bone. AMIRSYS ; 2013.
 
石田剛. 骨腫瘍の病理. 東京 : 文光堂 ; 2012.
 
P.370 掲載の参考文献
長谷川匡ほか編. 腫瘍病理鑑別アトラス : 軟部腫瘍. 東京 : 文光堂 ; 2011. p.191-6.
 
Deshpande V, et al. Epithelioid angiosarcoma of the bone : a series of 10 cases. Am J Surg Pathol. 2003 ; 27 : 709-16.
 
Fletcher CDM, et al. eds. World Health Organization Classification Tumours WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC Press, 2013.
 
P.374 掲載の参考文献
Yamada Y, et al. Sclerosing variant of perivascular epithelioid cell tumor in the female genital organs. Pathol Int. 2011 ; 61 (12) : 768-72.
PubMed
Hornick C-C Pan. PEComa JL. In : Fletcher CDM, et al. eds. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. Lyon : IARC Press ; 2013. p. 230-1.
 
P.378 掲載の参考文献
山元英崇. 炎症性筋線維芽細胞腫瘍. 長谷川匡, 小田義直編. 腫瘍鑑別診断アトラス軟部腫瘍. 東京 : 文光堂 ; 2011. p.26-31.
 
山元英崇, 小田義直. 炎症性筋線維芽細胞性腫瘍とその周辺疾患. 病理と臨床. 2012 ; 30 : 258-64.
Medical*Online
Marino-Enriquez A, et al. Epithelioid inflammatory myofibroblastic sarcoma : An aggressive intra-abdominal variant of inflammatory myofibroblastic tumor with nuclear membrane or perinuclear ALK. Am J Surg Pathol. 2011 ; 35 : 135-44.
PubMed
Yamamoto H, et al. Inflammatory myofibroblastic tumor versus IgG4-related sclerosing disease and inflammatory pseudotumor : a comparative clinicopathologic study. Am J Surg Pathol. 2009 ; 33 : 1330-40.
PubMed
P.382 掲載の参考文献
Bhattacharya B, et al. Nuclear beta-catenin expression distinguishes deep fibromatosis from other benign and malignant fibroblastic and myofibroblastic lesions. Am J Surg Pathol. 2005 ; 29 : 653-9.
PubMed
Evans HL. Low-grade fibromyxoid sarcoma : a report of two metastasizing neoplasms having a deceptively benign appearance. Am J Clin Pathol. 1987 ; 88 : 615-9.
PubMed
Doyle LA, et al. MUC4 is a highly sensitive and specific marker for low-grade fibromyxoid sarcoma. Am J Surg Pathol. 2011 ; 35 : 733-41.
PubMed
Matsuyama A, et al. Molecular detection of FUS-CREB3L2 fusion transcripts in low-grade fibromyxoid sarcoma using formalin-fixed, paraffin-embedded tissue specimens. Am J Surg Pathol. 2006 ; 30 : 1077-84.
PubMed
Mertens F, et al. Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene. Lab Invest. 2005 ; 85 : 408-15.
PubMed
Panagopoulos I, et al. The chimeric FUS/CREB3L2 gene is specific for low-grade fibromyxoid sarcoma. Genes Chromosomes Cancer. 2004 ; 40 : 218-28.
PubMed
P.386 掲載の参考文献
Oda Y, Tsuneyoshi M. Extrarenal rhabdoid tumors of soft tissue : clinicopathological and molecular genetic review and distinction from other soft-tissue sarcomas with rhabdoid features. Pathol Int. 2006 ; 56 : 287-95.
PubMed
Hollmann TJ, Hornick JL. INI1-deficient tumors : diagnostic features and molecular genetics. Am J Surg Pathol. 2011 ; 35 : e47-63.
PubMed
Kohashi K, et al. Glypican 3 expression in tumors with loss of SMARCB1/INI1 protein expression. Hum Pathol. 2013 ; 44 : 526-33.
PubMed
Fletcher CDM, Julia AB, eds. WHO Classification of Tumours of Soft Tissue and Bone. Lyon : IARC Press ; 2013.
 
P.390 掲載の参考文献
Folpe AL. Phosphaturic mesenchymal tumor. In : Fletcher DM, et al. eds. WHO Classification of Tumours of Soft Tissue and Bone. Geneva : World Health Organization ; 2013. p.211-2.
 
Weidner N, et al. Neoplastic pathology of oncogenic osteomalacia/rickets. Cancer. 1985 ; 55 : 1691-705.
PubMed
Weidner N, et al. Phosphaturic mesenchymal tumors, A polymorphous group causing osteomalacia or rickets. Cancer. 1987 ; 59 : 1442-54.
PubMed
Cai Q, et al. Inhibition of renal phosphate transport by a tumor product in a patient with oncogenic osteomalacia. N Engl J Med. 1994 ; 330 : 1645-49.
 
Shimada T, et al. Cloning and characterization of FGF23 as a causative factor of tumorinduced osteomalacia. PNAS. 2001 ; 98 : 6500-5.
PubMed
Toyosawa S, et al. Expression of dentin matrix protein 1 in tumors causing oncogenic osteomalacia. Mod Pathol. 2004 ; 17 : 537-8.
 
Folpe AL, et al. Most osteomalacia associated mesenchymal tumors are a single histopathologic entity. Am J Surg Pathol. 2004 ; 28 : 1-30.
PubMed
Bahrami A, et al. RT-PCR analysis for FGF23 using paraffin sections in the diagnosis of phosphaturic mesenchymal tumors with and without known tumor induced osteomalacia. Am J Surg Pathol. 2009 ; 33 : 1348-54.
PubMed
Bower RS, et al. Intracranial phosphaturic mesenchymal tumor, mixed connective tissue variant presenting without oncogenic osteomalacia. Surg Neurol Int. 2012 ; 3 : 151.
PubMed

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