中胚葉腎腫、中胚葉性腎腫、間葉芽腎腫、腎間葉芽腫
- 関
- congenital mesoblastic nephroma
WordNet
- relating to or derived from the mesoderm (同)mesodermal
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/05/24 17:51:54」(JST)
[Wiki en表示]
Mesoblastic nephroma |
Classification and external resources |
ICD-O: |
8960/1 |
MeSH |
D018201 |
Congenital mesoblastic nephroma is a type of kidney tumor that is usually found before birth by ultrasound or within the first 3 months of life. It contains fibroblastic cells (connective tissue cells), and may spread to the other kidney or to nearby tissue. Congenital mesoblastic nephroma is more common in males.
Differential diagnosis [edit]
A common differential diagnosis includes the following tumors:
- Mesoblastic nephroma (congenital): from birth to 1 year
- Rhabdoid tumor: from 1 to 2 years of age
- Clear cell sarcoma of kidney: from 2 to 3 years of age.
- Wilm's tumor: over 3 years of age.
The age breakdown is far from exact, but provides a useful age range and approximate order. Wilm's is most common, accounting for 80-85% of all pediatric kidney tumors. Congenital mesoblastic nephroma accounts for about 10-15%; rhabdoid and CCSK split the remained 5-10%.
External links [edit]
- Congenital mesoblastic nephroma entry in the public domain NCI Dictionary of Cancer Terms
This article incorporates public domain material from the U.S. National Cancer Institute document "Dictionary of Cancer Terms".
Connective/soft tissue tumors and sarcomas (ICD-O 8800–9059) (C45–C49/D17–D21, 171/214–215)
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Not otherwise specified (8800–8809) |
Soft tissue sarcoma · Desmoplastic small round cell tumor
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Connective tissue neoplasm |
Fibromatous (8810–8839)
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Fibroma/fibrosarcoma: Dermatofibrosarcoma · Dermatofibrosarcoma protuberans · Desmoplastic fibroma
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
Histiocytoma/histiocytic sarcoma: Benign fibrous histiocytoma · Malignant fibrous histiocytoma · Atypical fibroxanthoma
Solitary fibrous tumor
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Myxomatous (8840–8849)
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Myxoma/myxosarcoma (Cutaneous myxoma, Superficial acral fibromyxoma) · Angiomyxoma · Ossifying fibromyxoid tumour
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Fibroepithelial (9000–9039)
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Brenner tumour · Fibroadenoma · Phyllodes tumor
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Synovial-like (9040–9049)
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Synovial sarcoma · Clear-cell sarcoma
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Lipomatous (8850–8889) |
Lipoma/liposarcoma (Myelolipoma, Myxoid liposarcoma) · PEComa (Angiomyolipoma)
Chondroid lipoma · Intradermal spindle cell lipoma · Pleomorphic lipoma · Benign lipoblastomatosis · Spindle cell lipoma · Hibernoma
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Myomatous (8890–8929) |
general: Myoma/myosarcoma
smooth muscle: Leiomyoma/leiomyosarcoma
skeletal muscle: Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma (Sarcoma botryoides) · Alveolar rhabdomyosarcoma
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 (8930–8999) |
Adenomyoma · Pleomorphic adenoma · Mixed Müllerian tumor · Mesoblastic nephroma · Wilms' tumor · Rhabdoid tumour · Clear-cell sarcoma of the kidney · Hepatoblastoma · Pancreatoblastoma · Carcinosarcoma
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Mesothelial (9050–9059) |
Mesothelioma · Adenomatoid tumor
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see also Template:Connective tissue
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anat (h/n, u, t/d, a/p, l)/phys/devp/hist
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noco (m, s, c)/cong (d)/tumr, sysi/epon, injr
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Tumors: urogenital neoplasia: urinary organs (C64–C68/D30, 188–189/223)
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Abdominal |
Kidney
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Glandular and epithelial neoplasm: Renal cell carcinoma · Renal oncocytoma
Complex and mixed tumor: Wilms' tumor · Mesoblastic nephroma · Clear-cell sarcoma of the kidney · Angiomyolipoma · Cystic nephroma · Metanephric adenoma
by location: Renal medullary carcinoma · Juxtaglomerular cell tumor · Renal medullary fibroma
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Ureter
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Ureteral neoplasm
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Pelvic |
Bladder
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Transitional cell carcinoma · Inverted papilloma · Squamous cell carcinoma
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Urethra
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Transitional cell carcinoma · Squamous cell carcinoma · Adenocarcinoma · Melanoma
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Retroperitoneum |
Malignant fibrous histiocytoma
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noco/acba/cong/tumr, sysi/epon, urte
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proc/itvp, drug (G4B), blte, urte
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UpToDate Contents
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English Journal
- Intestinal congenital/infantile fibrosarcoma: a new clinico-pathological entity?
- Berrebi D1, Fournet JC, Boman F, Fabre M, Philippe-Chomette P, Branchereau S, Fréneaux P, Bouron-Dal Soglio D, Michon J, Peuchmaur M.
- Pediatric surgery international.Pediatr Surg Int.2015 Apr;31(4):375-9. doi: 10.1007/s00383-015-3670-7. Epub 2015 Feb 5.
- Congenital/infantile fibrosarcoma (IFS) is a relatively rare form of fibrosarcoma diagnosed at birth or during early years of life and that differs from its adult counterpart because of a more favorable behavior. IFS is also known as cellular congenital mesoblastic nephroma, when it affects the kidn
- PMID 25652760
- Congenital mesoblastic nephroma with focal anaplastic lesion.
- Yoshida M1, Okita H, Tanimoto T, Bitoh Y, Fukuzawa H, Yokoi A, Kozaki A, Kawasaki K, Akasaka Y.
- Pathology international.Pathol Int.2015 Mar 27. doi: 10.1111/pin.12293. [Epub ahead of print]
- PMID 25818639
- In vivo imaging of Aminopeptidase N (CD13) receptors in experimental renal tumors using the novel radiotracer (68)Ga-NOTA-c(NGR).
- Máté G1, Kertész I1, Enyedi KN2, Mező G2, Angyal J3, Vasas N4, Kis A1, Szabó É3, Emri M1, Bíró T4, Galuska L1, Trencsényi G5.
- European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.Eur J Pharm Sci.2015 Mar 10;69:61-71. doi: 10.1016/j.ejps.2015.01.002. Epub 2015 Jan 13.
- PURPOSE: Aminopeptidase N (APN/CD13) plays an important role in tumor neoangiogenic process and the development of metastases. Furthermore, it may serve as a potential target for cancer diagnosis and therapy. Previous studies have already shown that asparagine-glycine-arginine (NGR) peptides specifi
- PMID 25592229
Japanese Journal
- 過去25年間に経験した小児腎腫瘍20例の管理および長期予後に関する検討
- 長 祐子,飯塚 進,畑江 芳郎,武田 武夫,内藤 春彦,山城 勝重,有賀 正
- 小児がん : 小児悪性腫瘍研究会記録 47(1), 73-78, 2010-02-25
- 1984年から2008年3月に北海道がんセンター小児科が閉鎖するまでの約25年間に当施設で新規診断,治療が行われた15歳未満の腎腫瘍20例を対象とし,その臨床像,治療法,治療合併症,晩期障害,転帰に関して検討を行った.手術,NWTSに準じた化学療法,放射線療法を行ない,17例が長期生存を得た.しかし診断後10年近く経過したのちに放射線治療や単腎に関連すると思われる様々な晩期障害が観察された.
- NAID 110007575320
- 堀米 史子,藤原 利男,土岡 丘,岡本 健太郎,金子 恵,加藤 広行
- 日本小児外科学会雑誌 46(1), 48-52, 2010-02-20
- … 症例は生後3か月男児.富細胞型間葉芽腎腫cellular type mesoblastic nephroma (MN)の1例を報告する.哺乳不良を契機とし,長径約12cmの巨大な腹部腫瘤を認めた.腫瘍は乳白色充実性腫瘍でWilms腫瘍,腎明細胞肉腫との鑑別に難渋した.組織学的には,細胞密度の高い紡錘形細胞を主体とする腫瘍細胞が錯綜し,遺伝子検索にてETV6-NTRK3融合遺伝子RNAが検出され,臨床像と合わせ本疾患と診断した. …
- NAID 110007644567
Related Links
- 27 May 2011 ... Mesoblastic Nephroma Imaging. Neonatal tumors occur every 12500 to 27500 live births and account for 2% of childhood malignancies.
Related Pictures
★リンクテーブル★
[★]
- 英
- mesoblastic nephroma
- 関
- 中胚葉腎腫、間葉芽腎腫、腎間葉芽腫、先天性中胚葉腎腫
[★]
- 英
- mesoblastic nephroma
- 関
- 中胚葉性腎腫、間葉芽腎腫、腎間葉芽腫
[★]
- 英
- mesoblastic nephroma
- 関
- 中胚葉性腎腫、中胚葉腎腫、間葉芽腎腫
[★]
- 英
- mesoblastic nephroma
- 関
- 中胚葉性腎腫、中胚葉腎腫、腎間葉芽腫
[★]
- 関
- mesoblast、mesoderm、mesodermal
[★]
中胚葉
- 関
- mesoblastic、mesoderm、mesodermal
[★]
腎腫瘍、腎腫
- 関
- renal neoplasm