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Metanephric adenoma

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tubular structures of mature and bland appearance with scanty interposed stroma. Cells are small with dark staining nuclei and inconspicuous nucleoli. Blastema is absent whereas calcospherites may be present. Glomeruloid figures are a striking finding, reminiscent of early fetal metenephric tissue. The lumen of the acini may contain otherwise epithelial infoldings or fibrillary material but it is quite often empty. Mitoses are conspicuously absent. In the series reported by Jones
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found that intense and diffuse immunoreactivity for alpha-methylacyl-CoA racemase (AMACR) is useful in differentiating renal cell carcinoma from MA but a panel including AMACR, CK7 and CD57 is better in this differential diagnosis. Differential diagnosis may be quite difficult indeed as exemplified
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Metanephric adenoma is diagnosed histologically. The tumours can be located at upper pole, lower pole and mid-hilar region of the kidney; they are well circumscribed but unencapsulated, tan pink, with possible cystic and hemorrhagic foci. They show a uniform architecture of closely packed acinar or
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MA has been described in the past under other names such as néphrome néphronogène, metanephroider Nierentumor and nephroblastomartiges Nierenadenom (5) but the term metanephric adenoma was suggested by Brisigotti, Cozzutto et al. in 1992 and then widely accepted. Prior to this report, Nagashima et
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stated that genetic analysis of chromosome 7, 17, and Y may facilitate discrimination of MA from papillary renal cell carcinoma in difficult cases. Their study showed that MA lacks the frequent gain of chromosomes 7 and 17 and losses of the Y chromosome that are typical of papillary renal cell
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and a palpable mass. Mean age at onset is around 40 years with a range of 5 to 83 years and the mean size of the tumour is 5.5 cm with a range 0.3 to 15 cm (1). Polycythemia is more frequent in MA than in any other type of renal tumour. Of further relevance is that this tumour is more
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Jones EC, Pins M, Dickersin GR, Young RH (June 1995). "Metanephric adenoma of the kidney. A clinicopathological, immunohistochemical, flow cytometric, cytogenetic, and electron microscopic study of seven cases".
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tumour cells were reactive for Leu7 in 3 cases of 5, to vimentine in 4 of 6, to cytocheratin in 2 of 6, to epithelial membrane antigen in 1 of 6 cases and muscle specific antigen in 1 of 6. Olgac
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al. in 1991 had not offered a nosological innovation for their two cases whereas the denomination of néphrome néphronogène proposed by Pages and Granier in 1980 had gone largely undetected.
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Pins MR, Jones EC, Martul EV, Kamat BR, Umlas J, Renshaw AA (May 1999). "Metanephric adenoma-like tumors of the kidney: report of 3 malignancies with emphasis on discriminating features".
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commonly calcified than any other kidney neoplasm. Surgery is curative and no other treatment is recommended. There is so far no evidence of metastases or local recurrence.
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Nagashima Y, Arai N, Tanaka Y, Yoshida S, Sumino K, Ohaki Y, Matsushita K, Morita T, Misugi K (1991). "Two cases of a renal epithelial tumour resembling immature nephron".
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Bastos Netto JM, Esteves TC, Mattos R, Tibiriçá SH, Costa SM, Vieira LJ (August 2007). "Metanephric adenoma: a rare differential diagnosis of renal tumor in children".
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Olgac S, Hutchinson B, Tickoo SK, Reuter VE (February 2006). "Alpha-methylacyl-CoA racemase as a marker in the differential diagnosis of metanephric adenoma".
791: 570:"Metanephric adenoma lacks the gains of chromosomes 7 and 17 and loss of Y that are typical of papillary renal cell carcinoma and papillary adenoma" 1004: 340: 323: 284:
Davis CJ, Barton JH, Sesterhenn IA, Mostofi FK (October 1995). "Metanephric adenoma. Clinicopathological study of fifty patients".
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by the three malignancies initially diagnosed as MA that later metastasized, in the report by Pins et al.
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As metanephric adenomas are considered benign, they can be left in place, i.e. no treatment is needed.
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Brisigotti M, Cozzutto C, Fabbretti G, Sergi C, Callea F (October 1992). "Metanephric adenoma".
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Kovacs G, Akhtar M, Beckwith BJ, Bugert P, Cooper CS, Delahunt B, et al. (October 1997).
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neoplasms, suggesting that MA is not related to renal cell carcinoma and papillary adenoma.
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Grignon DJ, Eble JN (February 1998). "Papillary and metanephric adenomas of the kidney".
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Galmiche L, Vasiliu V, Poirée S, Hélénon O, Casanova JM, Brousse N (October 2007). "".
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It should not be confused with the pathologically unrelated, yet similar sounding,
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10.1002/(SICI)1096-9896(199710)183:2<131::AID-PATH931>3.0.CO;2-G
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Brunelli M, Eble JN, Zhang S, Martignoni G, Cheng L (October 2003).
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The symptoms may be similar to those classically associated with
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Pages A, Granier M (1980). "Le néphrome néphronogène".
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with structures reminiscent of those seen in papillary
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St Louis: Mosby. p. 118. 1005:Malignant fibrous histiocytoma 93:nephroblastoma (Wilms tumours) 1: 631:10.1016/s0242-6498(07)78275-5 445:Bostwick DG, Eble JN (2008). 547:10.5858/1999-123-0415-MALTOT 376:Histology and Histopathology 263:10.1016/j.jpurol.2006.10.003 251:Journal of Pediatric Urology 974:Transitional cell carcinoma 946:Transitional cell carcinoma 447:Urologic Surgical Pathology 206:Cytogenetic characteristics 1042: 901:Juxtaglomerular cell tumor 896:Renal medullary carcinoma 504:10.1038/modpathol.3800520 35: 26: 328:The Journal of Pathology 979:Squamous-cell carcinoma 951:Squamous-cell carcinoma 906:Renal medullary fibroma 1026:Benign renal neoplasms 697:Arch Anat Cytol Pathol 189: 166: 619:Annales de Pathologie 172: 149: 860:Mesoblastic nephroma 832:Renal cell carcinoma 118:renal cell carcinoma 97:renal cell carcinoma 45:renal cell carcinoma 880:Metanephric adenoma 178:metanephric adenoma 155:metanephric adenoma 105:mesonephric adenoma 78:Metanephric adenoma 41:metanephric adenoma 22:Metanephric adenoma 956:Inverted papilloma 666:10.1007/BF01600247 190: 167: 120:, and may include 1013: 1012: 928:Ureteral neoplasm 914: 913: 767: 766: 654:Virchows Archiv A 95:, or a papillary 75: 74: 16:Medical condition 1033: 837:Renal oncocytoma 822: 794: 787: 780: 771: 717: 705: 704: 692: 686: 685: 649: 643: 642: 614: 608: 607: 589: 574:Modern Pathology 565: 559: 558: 530: 524: 523: 492:Modern Pathology 487: 481: 480: 460: 451: 450: 442: 433: 432: 403: 392: 391: 371: 362: 361: 343: 319: 310: 309: 281: 275: 274: 246: 80:(MA) is a rare, 71: 70: 31: 19: 1041: 1040: 1036: 1035: 1034: 1032: 1031: 1030: 1016: 1015: 1014: 1009: 993: 960: 932: 910: 884: 875:Cystic nephroma 841: 811: 809:genital systems 798: 768: 763: 762: 728: 714: 709: 708: 694: 693: 689: 651: 650: 646: 616: 615: 611: 567: 566: 562: 532: 531: 527: 489: 488: 484: 462: 461: 454: 444: 443: 436: 405: 404: 395: 373: 372: 365: 321: 320: 313: 292:(10): 1101–14. 283: 282: 278: 248: 247: 243: 238: 229: 221: 208: 144: 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Index


Micrograph
renal cell carcinoma
H&E stain
Specialty
Oncology
Edit this on Wikidata
benign
tumour
kidney
nephroblastoma (Wilms tumours)
renal cell carcinoma
mesonephric adenoma
renal cell carcinoma
polycythemia
abdominal pain
hematuria

Micrograph
biopsy
PAS stain

Micrograph
biopsy
PAS stain
doi
10.1016/j.jpurol.2006.10.003
PMID
18947770
doi

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