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Journal Abstract Search

429 related items for PubMed ID: 19006426

  • 1. Morphologic Overlap between Infantile Myofibromatosis and Infantile Fibrosarcoma: A Pitfall in Diagnosis.
    Alaggio R, Barisani D, Ninfo V, Rosolen A, Coffin CM.
    Pediatr Dev Pathol; 2008; 11(5):355-62. PubMed ID: 19006426
    [Abstract] [Full Text] [Related]

  • 2. Congenital-infantile fibrosarcoma. A clinicopathologic study of 10 cases and molecular detection of the ETV6-NTRK3 fusion transcripts using paraffin-embedded tissues.
    Sheng WQ, Hisaoka M, Okamoto S, Tanaka A, Meis-Kindblom JM, Kindblom LG, Ishida T, Nojima T, Hashimoto H.
    Am J Clin Pathol; 2001 Mar; 115(3):348-55. PubMed ID: 11242790
    [Abstract] [Full Text] [Related]

  • 3. Primitive myxoid mesenchymal tumor of infancy: a clinicopathologic report of 6 cases.
    Alaggio R, Ninfo V, Rosolen A, Coffin CM.
    Am J Surg Pathol; 2006 Mar; 30(3):388-94. PubMed ID: 16538060
    [Abstract] [Full Text] [Related]

  • 4. Molecular detection of the ETV6-NTRK3 gene fusion differentiates congenital fibrosarcoma from other childhood spindle cell tumors.
    Bourgeois JM, Knezevich SR, Mathers JA, Sorensen PH.
    Am J Surg Pathol; 2000 Jul; 24(7):937-46. PubMed ID: 10895816
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  • 8. Are infantile myofibromatosis, congenital fibrosarcoma and congenital haemangiopericytoma histogenetically related?
    Variend S, Bax NM, van Gorp J.
    Histopathology; 1995 Jan; 26(1):57-62. PubMed ID: 7713484
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  • 9. A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma.
    Knezevich SR, McFadden DE, Tao W, Lim JF, Sorensen PH.
    Nat Genet; 1998 Feb; 18(2):184-7. PubMed ID: 9462753
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  • 10. Congenital/Infantile fibrosarcoma of the colon: morphologic, immunohistochemical, molecular, and ultrastructural features of a relatively rare tumor in an extraordinary localization.
    Buccoliero AM, Castiglione F, Rossi Degl'Innocenti D, Maio V, Taddei A, Sardi I, Noccioli B, Franchi A, Taddei GL.
    J Pediatr Hematol Oncol; 2008 Oct; 30(10):723-7. PubMed ID: 19011467
    [Abstract] [Full Text] [Related]

  • 11. Translocation-positive low-grade fibromyxoid sarcoma: clinicopathologic and molecular analysis of a series expanding the morphologic spectrum and suggesting potential relationship to sclerosing epithelioid fibrosarcoma: a study from the French Sarcoma Group.
    Guillou L, Benhattar J, Gengler C, Gallagher G, Ranchère-Vince D, Collin F, Terrier P, Terrier-Lacombe MJ, Leroux A, Marquès B, Aubain Somerhausen Nde S, Keslair F, Pedeutour F, Coindre JM.
    Am J Surg Pathol; 2007 Sep; 31(9):1387-402. PubMed ID: 17721195
    [Abstract] [Full Text] [Related]

  • 12. Generalized infantile myofibromatosis with a monophasic primitive pattern.
    Iwafuchi H, Tsuzuki T, Ito R, Miyake H, Okita H, Hamazaki M.
    Pathol Int; 2015 Aug; 65(8):432-7. PubMed ID: 25989870
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  • 13. Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma.
    Rubin BP, Chen CJ, Morgan TW, Xiao S, Grier HE, Kozakewich HP, Perez-Atayde AR, Fletcher JA.
    Am J Pathol; 1998 Nov; 153(5):1451-8. PubMed ID: 9811336
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  • 14. Anaplastic sarcoma of the kidney: a clinicopathologic study of 20 cases of a new entity with polyphenotypic features.
    Vujanić GM, Kelsey A, Perlman EJ, Sandstedt B, Beckwith JB.
    Am J Surg Pathol; 2007 Oct; 31(10):1459-68. PubMed ID: 17895746
    [Abstract] [Full Text] [Related]

  • 15. CD34-positive infantile myofibromatosis: Case report and review of hemangiopericytoma-like pattern tumors.
    Kiyohara T, Maruta N, Iino S, Ido H, Tokuriki A, Hasegawa M.
    J Dermatol; 2016 Sep; 43(9):1088-91. PubMed ID: 27074874
    [Abstract] [Full Text] [Related]

  • 16. Infantile NTRK-associated Mesenchymal Tumors.
    Davis JL, Lockwood CM, Albert CM, Tsuchiya K, Hawkins DS, Rudzinski ER.
    Pediatr Dev Pathol; 2018 Sep; 21(1):68-78. PubMed ID: 28683589
    [Abstract] [Full Text] [Related]

  • 17. Congenital myofibromatosis in two siblings.
    Arcangeli F, Calista D.
    Eur J Dermatol; 2006 Sep; 16(2):181-3. PubMed ID: 16581573
    [Abstract] [Full Text] [Related]

  • 18. Congenital fibrosarcoma with a novel complex 3-way translocation t(12;15;19) and unusual histologic features.
    Mariño-Enríquez A, Li P, Samuelson J, Rossi MR, Reyes-Múgica M.
    Hum Pathol; 2008 Dec; 39(12):1844-8. PubMed ID: 18657299
    [Abstract] [Full Text] [Related]

  • 19. ETV6-NTRK3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma.
    Knezevich SR, Garnett MJ, Pysher TJ, Beckwith JB, Grundy PE, Sorensen PH.
    Cancer Res; 1998 Nov 15; 58(22):5046-8. PubMed ID: 9823307
    [Abstract] [Full Text] [Related]

  • 20. Myofibromatosis in adults, glomangiopericytoma, and myopericytoma: a spectrum of tumors showing perivascular myoid differentiation.
    Granter SR, Badizadegan K, Fletcher CD.
    Am J Surg Pathol; 1998 May 15; 22(5):513-25. PubMed ID: 9591720
    [Abstract] [Full Text] [Related]

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