胎児性横紋筋腫型腎芽腫
WordNet
- of or relating to a fetus; "fetal development" (同)foetal
UpToDate Contents
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English Journal
- Supraorbital cutaneous fetal rhabdomyoma of intermediate type: a case report.
- Yang SH1, McCalmont TH, Ahn GG, Yeh I.
- The American Journal of dermatopathology.Am J Dermatopathol.2014 May;36(5):e93-6. doi: 10.1097/01.dad.0000441941.83273.c5.
- A 7-year-old boy was presented with a long-standing slowly growing mass of the left supraorbital area. A biopsy specimen revealed a bland spindle cell proliferation with scattered polygonal cells with acidophilic cytoplasm and cross-striations. Our differential diagnosis included rhabdomyoma of feta
- PMID 24803069
- Fine needle aspiration cytology of fetal rhabdomyomatous and teratoid Wilms tumor.
- Nayak A1, Iyer VK, Agarwal S, Agarwala S.
- Acta cytologica.Acta Cytol.2010 Jul-Aug;54(4):563-8.
- OBJECTIVE: To review nephrectomy specimens for pediatric renal tumors seen over a period of 9 years (1995-2003).STUDY DESIGN: Specimens categorized as fetal rhabdomyomatous Wilms tumors (WTs) or teratoid WTs were selected. Corresponding fine needle aspiration cytology slides were subjected to cytomo
- PMID 20715657
- Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome.
- Uccini S1, Perotti D, Colarossi C, Stoppacciaro A, Sardella M, Mannarino O, Collini P, Casieri P, Cozzi D, Amoroso L, Spreafico F, Radice P, Dominici C.
- Pediatric blood & cancer.Pediatr Blood Cancer.2008 Sep;51(3):344-8. doi: 10.1002/pbc.21507.
- BACKGROUND: This study investigated the genetic events leading to tumorigenesis in a patient affected with WAGR syndrome who developed multiple distinct Wilms tumors (WTs).PROCEDURE AND RESULTS: At 1 year of age, the child developed two synchronous bilateral WTs that were resected by partial nephrec
- PMID 18293378
Japanese Journal
- Responsiveness of chemotherapy based on the histological type and Wilms' tumor suppressor gene mutation in bilateral Wilms' tumor
- Fetal rhabdomyomatous nephroblastoma : a tumour of good prognosis but resistant to chemotherapy
Related Links
- Fetal rhabdomyomatous nephroblastoma is a very rare variant of Wilms' tumor. The special clinical and histologic features of this variant are presented on the basis of a case seen in a boy who was 13
- [Show abstract] [Hide abstract] ABSTRACT: The present report describes the case of a 21-mo-old boy with a fetal rhabdomyomatous nephroblastoma (FRN) diagnosed by fine-needle aspiration cytology (FNAC). The smears contained ...
★リンクテーブル★
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- 英
- fetal rhabdomyomatous nephroblastoma
- 同
- 類奇形腎芽腫 teratoid nephroblastoma、類奇形ウィルムス腫瘍 teratoid Wilms tumor
[★]
- 胎生期の、胎性の、(人間)胎児の、胎児性の、(動物)胎仔の、胎仔型の
- 関
- embryo、embryonal、embryonic、embryonic day、embryonic form、embryonic stage、fetal stage、feto、fetus、foetal、foetus