WordNet
- present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
- relating to or derived from the mesoderm (同)mesodermal
PrepTutorEJDIC
- (病気・身体的欠陥など)生まれつきの,先天的な
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2013/02/25 09:30:23」(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
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
- 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)
|
|
| Not otherwise specified (8800–8809) |
Soft tissue sarcoma · Desmoplastic small round cell tumor
|
|
| Connective tissue neoplasm |
|
Fibromatous (8810–8839)
|
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
|
|
|
Myxomatous (8840–8849)
|
Myxoma/myxosarcoma (Cutaneous myxoma, Superficial acral fibromyxoma) · Angiomyxoma · Ossifying fibromyxoid tumour
|
|
|
Fibroepithelial (9000–9039)
|
Brenner tumour · Fibroadenoma · Phyllodes tumor
|
|
|
Synovial-like (9040–9049)
|
Synovial sarcoma · Clear-cell sarcoma
|
|
|
| Lipomatous (8850–8889) |
Lipoma/liposarcoma (Myelolipoma, Myxoid liposarcoma) · PEComa (Angiomyolipoma)
Chondroid lipoma · Intradermal spindle cell lipoma · Pleomorphic lipoma · Benign lipoblastomatosis · Spindle cell lipoma · Hibernoma
|
|
| 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
|
|
| 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
|
|
| Mesothelial (9050–9059) |
Mesothelioma · Adenomatoid tumor
|
|
|
see also Template:Connective tissue
|
|
anat (h/n, u, t/d, a/p, l)/phys/devp/hist
|
noco (m, s, c)/cong (d)/tumr, sysi/epon, injr
|
|
|
|
|
|
Tumors: urogenital neoplasia: urinary organs (C64–C68/D30, 188–189/223)
|
|
| Abdominal |
|
Kidney
|
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
|
|
|
Ureter
|
Ureteral neoplasm
|
|
|
| Pelvic |
|
Bladder
|
Transitional cell carcinoma · Inverted papilloma · Squamous cell carcinoma
|
|
|
Urethra
|
Transitional cell carcinoma · Squamous cell carcinoma · Adenocarcinoma · Melanoma
|
|
|
| Retroperitoneum |
Malignant fibrous histiocytoma
|
|
|
|
|
noco/acba/cong/tumr, sysi/epon, urte
|
proc/itvp, drug (G4B), blte, urte
|
|
|
|
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Congenital mesoblastic nephroma in a premature neonate: A case report and review of literature.
- Anunobi CC1, Badmos KB, Onyekwelu VI, Ikeri NZ.Author information 1Department of Anatomic and Molecular Pathology, College of Medicine, University of Lagos and Lagos University Teaching Hospital, Lagos, Nigeria.AbstractCongenital mesoblastic nephroma (CMN) is a renal stromal neoplasm of infancy. It comprises 3-10% of all pediatric renal tumors. We report a case of CMN in a 30 week old premature female neonate seen at autopsy who was born to a 26-year-old woman by emergency cesarean section on account of polyhydramnios.
- Nigerian journal of clinical practice.Niger J Clin Pract.2014 Mar-Apr;17(2):255-9. doi: 10.4103/1119-3077.127573.
- Congenital mesoblastic nephroma (CMN) is a renal stromal neoplasm of infancy. It comprises 3-10% of all pediatric renal tumors. We report a case of CMN in a 30 week old premature female neonate seen at autopsy who was born to a 26-year-old woman by emergency cesarean section on account of polyhydram
- PMID 24553043
- Maternal manifestation of Ballantyne's syndrome occurring concomitantly with the development of fetal congenital mesoblastic nephroma.
- Takahashi H1, Matsubara S, Kuwata T, Ohkuchi A, Mukoda Y, Saito K, Usui R, Suzuki M.Author information 1Department of Obstetrics and Gynecology, Jichi Medical University, Tochigi, Japan.AbstractVarious fetal or placental disorders cause Ballantyne's (mirror) syndrome. For the first time, we report a maternal manifestation of Ballantyne's syndrome occurring concomitantly with the development of fetal congenital mesoblastic nephroma (CMN). In a pregnant woman with a CMN fetus, lung edema, hypertension, hyperthyroidism, and high serum human chorionic gonadotrophin level occurred, all of which characterize maternal manifestation of Ballantyne's syndrome. The fetus and placenta were devoid of 'edema', lacking 'triple edema', and thus this condition was not diagnosed as Ballantyne's syndrome; however, we considered this condition as the maternal manifestation of Ballantyne's syndrome. We performed emergent cesarean section at 28 weeks. Delivery acutely ameliorated maternal symptoms. Tumor was resected and was confirmed as CMN. Maternal manifestations of Ballantyne's syndrome, such as lung edema and hypertension, can occur in a mother with fetal CMN even without fetal and/or placental edema. The clinical course of this patient may suggest an etiology of Ballantyne's syndrome.
- The journal of obstetrics and gynaecology research.J Obstet Gynaecol Res.2014 Jan 15. doi: 10.1111/jog.12286. [Epub ahead of print]
- Various fetal or placental disorders cause Ballantyne's (mirror) syndrome. For the first time, we report a maternal manifestation of Ballantyne's syndrome occurring concomitantly with the development of fetal congenital mesoblastic nephroma (CMN). In a pregnant woman with a CMN fetus, lung edema, hy
- PMID 24428571
- Prenatal sonographic diagnosis of multicystic congenital mesoblastic nephroma.
- Esmer AC1, Kalelioglu I, Kilicaslan I, Gun F, Ziylan O.Author information 1Department of Obstetrics and Gynecology, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey.AbstractThe authors report an unusual presentation of congenital mesoblastic nephroma as a multilocular cystic renal lesion. Prenatal sonography revealed a unilateral, encapsulated, multilocular cystic mass with solid components measuring 5.7 × 5.4 × 4.3 cm in the left renal fossa. There was no increase in vascularity and no signs of hydrops fetalis. On the forth postnatal day left-sided radical nephrectomy was performed and histopathological examination revealed cellular type congenital mesoblastic nephroma. A multicystic appearance is rare as the vast majority of prenatally diagnosed congenital mesoblastic nephroma cases presented in the literature are of the classic type with solid homogenous or heterogenous appearence.
- Journal of clinical ultrasound : JCU.J Clin Ultrasound.2013 Nov-Dec;41 Suppl 1:59-61. doi: 10.1002/jcu.22032. Epub 2012 Dec 27.
- The authors report an unusual presentation of congenital mesoblastic nephroma as a multilocular cystic renal lesion. Prenatal sonography revealed a unilateral, encapsulated, multilocular cystic mass with solid components measuring 5.7 × 5.4 × 4.3 cm in the left renal fossa. There was no increase i
- PMID 23280386
Japanese Journal
- Pathology : Histopathological, Immunohistochemical and Ultrastructural Studies of a Renal Mesenchymal Tumor in a Young Beagle Dog
- SUZUKI Yui,TAKABA Katsumi,YAMAGUCHI Itaru [他]
- The journal of veterinary medical science 74(1), 89-92, 2012-01-00
- NAID 40019170821
- Histopathological, Immunohistochemical and Ultrastructural Studies of a Renal Mesenchymal Tumor in a Young Beagle Dog
- SUZUKI Yui,TAKABA Katsumi,YAMAGUCHI Itaru,MYOUJOU Kensuke,KIMOTO Naoya,IKEGAMI Hisashi,SAEKI Koji,IMAIZUMI Minami,TAKADA Chie
- Journal of Veterinary Medical Science 74(1), 89-92, 2012
- … Based on the microscopic findings, interstitial characteristics and immunohistochemical features, the present case was classified as a congenital mesoblastic tumor.<br> …
- NAID 130001032841
Related Links
- Sir, Congenital mesoblastic nephroma (CMN) tumor is most common benign renal neoplasm in neonates and infants less than 3 months of age, and overall comprises about 3-10% of all childhood renal tumors.[1] Mesoblastic ...
- Congenital Mesoblastic Nephroma Pages with reference to book, From 238 To 240 Zafar Zaidi, Pierre Mouriquand (Department of Paediatric Urology, Great Ormond Street Hospital for Children, London, United Kingdom. )
★リンクテーブル★
[★]
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
[★]
- 英
- congenital mesoblastic nephroma
- 関
- 中胚葉性腎腫
[★]
- 関
- congenital、congenitally
[★]
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
[★]
- 関
- mesoblast、mesoderm、mesodermal
[★]
中胚葉
- 関
- mesoblastic、mesoderm、mesodermal
[★]