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Quoted phrase not found in phrase index: "Myofibromatosis, infantile, 2"
Page 1
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. Kiyohara T, et al. J Dermatol. 2016 Sep;43(9):1088-91. doi: 10.1111/1346-8138.13400. Epub 2016 Apr 14. J Dermatol. 2016. PMID: 27074874 Review.
We describe a case of CD34-positive infantile myofibromatosis with hemangiopericytoma-like pattern. A 2-day-old Japanese boy presented with multiple hemispherical nodules on the extremities and back. ...
We describe a case of CD34-positive infantile myofibromatosis with hemangiopericytoma-like pattern. A 2-day-old Japanese boy presente …
Prenatal diagnosis of infantile myofibromatosis of the lung: a case report and review of the literature.
Yeniel AO, Ergenoglu AM, Zeybek B, Kazandi M, Akercan F, Ozcan C, Veral A. Yeniel AO, et al. J Clin Ultrasound. 2013 Nov-Dec;41 Suppl 1:38-41. doi: 10.1002/jcu.22059. Epub 2013 May 20. J Clin Ultrasound. 2013. PMID: 23686518 Review.
The fetus was monitored with weekly ultrasound examinations measuring the mass size and amniotic fluid index. On day 2 after delivery, due to respiratory distress, an exploratory thoracotomy was undertaken and the mass was resected....
The fetus was monitored with weekly ultrasound examinations measuring the mass size and amniotic fluid index. On day 2 after delivery …
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis.
Arts FA, Sciot R, Brichard B, Renard M, de Rocca Serra A, Dachy G, Noël LA, Velghe AI, Galant C, Debiec-Rychter M, Van Damme A, Vikkula M, Helaers R, Limaye N, Poirel HA, Demoulin JB. Arts FA, et al. Hum Mol Genet. 2017 May 15;26(10):1801-1810. doi: 10.1093/hmg/ddx081. Hum Mol Genet. 2017. PMID: 28334876
Novel PDGFRB rearrangement in multifocal infantile myofibromatosis is tumorigenic and sensitive to imatinib.
Hassan M, Butler E, Wilson R, Roy A, Zheng Y, Liem P, Rakheja D, Pavlick D, Young LL, Rosenzweig M, Erlich R, Ali SM, Leavey PJ, Parsons DW, Skapek SX, Laetsch TW. Hassan M, et al. Cold Spring Harb Mol Case Stud. 2019 Oct 23;5(5):a004440. doi: 10.1101/mcs.a004440. Print 2019 Oct. Cold Spring Harb Mol Case Stud. 2019. PMID: 31645346 Free PMC article.
Ectopic expression of cDNA encoding the mutant form of PDGFRB markedly enhanced cell proliferation of mouse embryo fibroblasts (MEFs) compared to wild-type PDGFRB and conferred tumor-forming capacity on nontumorigenic 10T1/2 fibroblasts. The mutated protein enhanced MAPK a …
Ectopic expression of cDNA encoding the mutant form of PDGFRB markedly enhanced cell proliferation of mouse embryo fibroblasts (MEFs) compar …
Infantile myofibromatosis: a series of 28 cases.
Mashiah J, Hadj-Rabia S, Dompmartin A, Harroche A, Laloum-Grynberg E, Wolter M, Amoric JC, Hamel-Teillac D, Guero S, Fraitag S, Bodemer C. Mashiah J, et al. J Am Acad Dermatol. 2014 Aug;71(2):264-70. doi: 10.1016/j.jaad.2014.03.035. Epub 2014 Jun 2. J Am Acad Dermatol. 2014. PMID: 24894456
Paediatric and adult soft tissue sarcomas with NTRK1 gene fusions: a subset of spindle cell sarcomas unified by a prominent myopericytic/haemangiopericytic pattern.
Haller F, Knopf J, Ackermann A, Bieg M, Kleinheinz K, Schlesner M, Moskalev EA, Will R, Satir AA, Abdelmagid IE, Giedl J, Carbon R, Rompel O, Hartmann A, Wiemann S, Metzler M, Agaimy A. Haller F, et al. J Pathol. 2016 Apr;238(5):700-10. doi: 10.1002/path.4701. J Pathol. 2016. PMID: 26863915
Neoplasms with a myopericytomatous pattern represent a morphological spectrum of lesions encompassing myopericytoma of the skin and soft tissue, angioleiomyoma, myofibromatosis/infantile haemangiopericytoma and putative neoplasms reported as malignant myopericytoma. …
Neoplasms with a myopericytomatous pattern represent a morphological spectrum of lesions encompassing myopericytoma of the skin and soft tis …
Expression of ALK1 and p80 in inflammatory myofibroblastic tumor and its mesenchymal mimics: a study of 135 cases.
Cessna MH, Zhou H, Sanger WG, Perkins SL, Tripp S, Pickering D, Daines C, Coffin CM. Cessna MH, et al. Mod Pathol. 2002 Sep;15(9):931-8. doi: 10.1097/01.MP.0000026615.04130.1F. Mod Pathol. 2002. PMID: 12218210
No staining was observed in nodular fasciitis, desmoid, infantile myofibromatosis, infantile fibrosarcoma, synovial sarcoma, leiomyoma, or myofibrosarcoma. ...
No staining was observed in nodular fasciitis, desmoid, infantile myofibromatosis, infantile fibrosarcoma, synovial sarcoma, l …
A Rare Case of Infantile Myofibromatosis Presenting to the Emergency Department as Undiagnosed Long Bone Fractures.
McGuire MA, Hendry PL, Hong N. McGuire MA, et al. Pediatr Emerg Care. 2017 Nov;33(11):e134-e136. doi: 10.1097/PEC.0000000000001325. Pediatr Emerg Care. 2017. PMID: 29095782
Infantile myofibromatosis is a disorder of mesenchymal tumors that usually presents within the first 2 years of life. Most patients initially present because of the presence of visible or palpable subcutaneous tumors. ...
Infantile myofibromatosis is a disorder of mesenchymal tumors that usually presents within the first 2 years of life. Most patients i …
A patient with germ-line gain-of-function PDGFRB p.N666H mutation and marked clinical response to imatinib.
Pond D, Arts FA, Mendelsohn NJ, Demoulin JB, Scharer G, Messinger Y. Pond D, et al. Genet Med. 2018 Jan;20(1):142-150. doi: 10.1038/gim.2017.104. Epub 2017 Jul 20. Genet Med. 2018. PMID: 28726812 Free article.
Patient fibroblasts showed constitutive receptor tyrosine phosphorylation that was also abrogated by imatinib with reduced proliferation of treated cells.This led to patient treatment with imatinib at 400 mg daily (340 mg/m(2)) for a year with objective improvement of debi …
Patient fibroblasts showed constitutive receptor tyrosine phosphorylation that was also abrogated by imatinib with reduced proliferation of …
Congenital infantile myofibroma causing intrauterine death in a twin.
Aye CY, Gould S, Akinsola SA. Aye CY, et al. BMJ Case Rep. 2011 Dec 1;2011:bcr0920114851. doi: 10.1136/bcr.09.2011.4851. BMJ Case Rep. 2011. PMID: 22674951 Free PMC article.
The authors report a 33-year-old para 1 with an uncomplicated, dichorionic diamniotic twin pregnancy who was diagnosed with an intrauterine death of one twin at 36+5 weeks gestation. At caesarean section, a macerated male stillborn weighing 2.72 kg was delivered. Postmorte …
The authors report a 33-year-old para 1 with an uncomplicated, dichorionic diamniotic twin pregnancy who was diagnosed with an intrauterine …