WordNet
- a highly malignant neoplasm derived from striated muscle (同)rhabdosarcoma
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/12/28 11:07:42」(JST)
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Embryonal rhabdomyosarcoma |
Classification and external resources |
OMIM |
268210 180295 |
DiseasesDB |
1557 |
Embryonal rhabdomyosarcoma (ERMS) is a rare histological form of cancer of connective tissue wherein the mesenchymally-derived malignant cells resemble the primitive developing skeletal muscle of the embryo. It is the most common soft tissue sarcoma occurring in children.[1]
Classification
ERMS is the more common of two major subtypes of rhabdomyosarcoma, the other being alveolar rhabdomyosarcoma.
It has been informally classified as a "small round blue cell tumor"[1] because of the characteristic microscopic appearance of its cells after histological staining with hematoxylin and eosin.
Prognosis and survival
The prognosis for rhabdomyosarcoma has improved greatly in recent decades, with over 70% of patients surviving for five years after diagnosis.[2]
References
- ^ a b Masola V, Maran C, Tassone E, Zin A, Rosolen A, Onisto M (2009). "Heparanase activity in alveolar and embryonal rhabdomyosarcoma: implications for tumor invasion". BMC Cancer 9: 304. doi:10.1186/1471-2407-9-304. PMC 2743710. PMID 19715595.
- ^ Breitfeld PP, Meyer WH (August 2005). "Rhabdomyosarcoma: new windows of opportunity". Oncologist 10 (7): 518–27. doi:10.1634/theoncologist.10-7-518. PMID 16079319.
Connective/soft tissue tumors and sarcomas (ICD-O 8800–9059) (C45–C49/D17–D21, 171/214–215)
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Not otherwise specified |
- Soft-tissue sarcoma
- Desmoplastic small-round-cell tumor
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Connective tissue neoplasm |
Fibromatous |
Fibroma/fibrosarcoma: |
- Dermatofibrosarcoma protuberans
- Desmoplastic fibroma
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Fibroma/fibromatosis: |
- Aggressive infantile fibromatosis
- Aponeurotic fibroma
- Collagenous fibroma
- Diffuse infantile fibromatosis
- Familial myxovascular fibromas
- Fibroma of tendon sheath
- Fibromatosis colli
- Infantile digital fibromatosis
- Juvenile hyaline fibromatosis
- Plantar fibromatosis
- Pleomorphic fibroma
- Oral submucous fibrosis
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Histiocytoma/histiocytic sarcoma: |
- Benign fibrous histiocytoma
- Malignant fibrous histiocytoma
- Atypical fibroxanthoma
- Solitary fibrous tumor
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Myxomatous |
- Myxoma/myxosarcoma
- Cutaneous myxoma
- Superficial acral fibromyxoma
- Angiomyxoma
- Ossifying fibromyxoid tumour
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Fibroepithelial |
- Brenner tumour
- Fibroadenoma
- Phyllodes tumor
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Synovial-like |
- Synovial sarcoma
- Clear-cell sarcoma
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Lipomatous |
- Lipoma/liposarcoma
- Myelolipoma
- Myxoid liposarcoma
- PEComa
- Chondroid lipoma
- Intradermal spindle cell lipoma
- Pleomorphic lipoma
- Lipoblastomatosis
- Spindle cell lipoma
- Hibernoma
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Myomatous |
general: |
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smooth muscle: |
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skeletal muscle: |
- Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma
- Alveolar rhabdomyosarcoma
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- Leiomyoma
- Angioleiomyoma
- Angiolipoleiomyoma
- Genital leiomyoma
- Leiomyosarcoma
- Multiple cutaneous and uterine leiomyomatosis syndrome
- Multiple cutaneous leiomyoma
- Neural fibrolipoma
- Solitary cutaneous leiomyoma
- STUMP
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Complex mixed and stromal |
- Adenomyoma
- Pleomorphic adenoma
- Mixed Müllerian tumor
- Mesoblastic nephroma
- Wilms' tumor
- Malignant rhabdoid tumour
- Clear-cell sarcoma of the kidney
- Hepatoblastoma
- Pancreatoblastoma
- Carcinosarcoma
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Mesothelial |
- Mesothelioma
- Adenomatoid tumor
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Index of muscle
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Description |
- Anatomy
- head
- neck
- arms
- chest and back
- diaphragm
- abdomen
- genital area
- legs
- Muscle tissue
- Physiology
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Disease |
- Myopathy
- Soft tissue
- Connective tissue
- Congenital
- abdomen
- muscular dystrophy
- Neoplasms and cancer
- Injury
- Symptoms and signs
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Treatment |
- Procedures
- Drugs
- anti-inflammatory
- muscle relaxants
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UpToDate Contents
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English Journal
- Histopathological, immunohistochemical and molecular cytogenetic analysis of 21 spindle cell/sclerosing rhabdomyosarcomas.
- Rekhi B1, Singhvi T.
- APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.APMIS.2014 Nov;122(11):1144-52. doi: 10.1111/apm.12272. Epub 2014 Apr 14.
- Recently, spindle cell/sclerosing rhabdomyosarcoma (RMS) has been recognized as another distinct variant of a RMS. We evaluated clinicopathological features of 21 cases of spindle cell and sclerosing RMS and performed fluorescent in situ hybridization (FISH) testing in 10 (47.6%) tumours. Twenty-one
- PMID 24730567
- Preliminary Results of a Phase II Trial of Proton Radiotherapy for Pediatric Rhabdomyosarcoma.
- Ladra MM1, Szymonifka JD1, Mahajan A1, Friedmann AM1, Yong Yeap B1, Goebel CP1, MacDonald SM1, Grosshans DR1, Rodriguez-Galindo C1, Marcus KJ1, Tarbell NJ1, Yock TI2.
- Journal of clinical oncology : official journal of the American Society of Clinical Oncology.J Clin Oncol.2014 Oct 20. pii: JCO.2014.56.1548. [Epub ahead of print]
- PURPOSE: This prospective phase II study was designed to assess disease control and to describe acute and late adverse effects of treatment with proton radiotherapy in children with rhabdomyosarcoma (RMS).PATIENTS AND METHODS: Fifty-seven patients with localized RMS (age 21 years or younger) or meta
- PMID 25332253
Japanese Journal
- 筋発生分化と横紋筋肉腫の発生病態 (特集 個体発生と細胞分化の医学)
- 膀胱全摘出術によって長期生存を認めた犬の横紋筋肉腫の1例
- 志賀 大輔,三品 美夏,青木 大 [他],石井 宏志,渡邊 俊文
- 日本獣医師会雑誌 = Journal of the Japan Veterinary Medical Association 65(7), 525-529, 2012-07-20
- 1歳3カ月齢,未去勢のラブラドール・レトリバーが,血尿,頻尿を主訴に来院した。身体検査にて,下腹部に腫瘤を認め,超音波検査,X線膀胱造影検査を実施したところ,膀胱三角部全域にわたる膀胱腫瘤が確認されたため,膀胱全摘出術が実施された。摘出した膀胱は病理組織学的検査により胎児型横紋筋肉腫と診断された。手術後は,化学療法を1回実施したが,その後は飼い主の希望により経過観察とした。現在,術後約6年が経過し …
- NAID 10030800987
Related Pictures
★リンクテーブル★
[★]
- 英
- embryonal rhabdomyosarcoma
- 関
- 胎児性横紋筋肉腫
[★]
- 関
- embryonic、embryonic day、embryonic stage、embryonically、fetal、fetal stage