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1975 1
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1993 4
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2003 1
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Quoted phrase not found in phrase index: "Childhood Undifferentiated Pleomorphic Sarcoma"
Page 1
The proteomic landscape of soft tissue sarcomas.
Burns J, Wilding CP, Krasny L, Zhu X, Chadha M, Tam YB, Ps H, Mahalingam AH, Lee ATJ, Arthur A, Guljar N, Perkins E, Pankova V, Jenks A, Djabatey V, Szecsei C, McCarthy F, Ragulan C, Milighetti M, Roumeliotis TI, Crosier S, Finetti M, Choudhary JS, Judson I, Fisher C, Schuster EF, Sadanandam A, Chen TW, Williamson D, Thway K, Jones RL, Cheang MCU, Huang PH. Burns J, et al. Nat Commun. 2023 Jun 29;14(1):3834. doi: 10.1038/s41467-023-39486-2. Nat Commun. 2023. PMID: 37386008 Free PMC article.
Within leiomyosarcomas, we identify three proteomic subtypes with distinct myogenesis and immune features, anatomical site distribution and survival outcomes. Characterisation of undifferentiated pleomorphic sarcomas and dedifferentiated liposarcomas with low infilt …
Within leiomyosarcomas, we identify three proteomic subtypes with distinct myogenesis and immune features, anatomical site distribution and …
Primary histiocytic dermatoses.
Ringel E, Moschella S. Ringel E, et al. Arch Dermatol. 1985 Dec;121(12):1531-41. Arch Dermatol. 1985. PMID: 2998286 Review.
The malignant histiocytosis with erythrophagocytosis, the pseudomalignant histiocytic diseases (such as sinus histiocytosis with massive lymphadenopathy and regressing atypical histiocytosis), and the solitary lesions with histologic malignant and atypical storiform …
The malignant histiocytosis with erythrophagocytosis, the pseudomalignant histiocytic diseases (such as sinus histiocytosis with mass …
Etiopathogenic role of ERK5 signaling in sarcoma: prognostic and therapeutic implications.
Sánchez-Fdez A, Matilla-Almazán S, Del Carmen S, Abad M, Arconada-Luque E, Jiménez-Suárez J, Chinchilla-Tábora LM, Ruíz-Hidalgo MJ, Sánchez-Prieto R, Pandiella A, Esparís-Ogando A. Sánchez-Fdez A, et al. Exp Mol Med. 2023 Jun;55(6):1247-1257. doi: 10.1038/s12276-023-01008-x. Epub 2023 Jun 19. Exp Mol Med. 2023. PMID: 37332046 Free PMC article.
By developing a mouse model engineered to express a constitutively active form of MEK5, we demonstrate that the exclusive activation of the MEK5/ERK5 pathway can promote sarcomagenesis. Histopathological analyses identified these tumors as undifferentiated pleomorphic …
By developing a mouse model engineered to express a constitutively active form of MEK5, we demonstrate that the exclusive activation of the …
The role of radiology in paediatric soft tissue sarcomas.
Park K, van Rijn R, McHugh K. Park K, et al. Cancer Imaging. 2008 Apr 22;8(1):102-15. doi: 10.1102/1470-7330.2008.0014. Cancer Imaging. 2008. PMID: 18442956 Free PMC article. Review.
Paediatric soft tissue sarcomas (STS) are a group of malignant tumours that originate from primitive mesenchymal tissue and account for 7% of all childhood tumours. Rhabdomyosarcomas (RMS) and undifferentiated sarcomas account for approximately 50% of soft ti …
Paediatric soft tissue sarcomas (STS) are a group of malignant tumours that originate from primitive mesenchymal tissue and account f …
Rhabdomyosarcoma in childhood.
Bale PM, Reye RD. Bale PM, et al. Pathology. 1975 Apr;7(2):101-11. doi: 10.3109/00313027509092704. Pathology. 1975. PMID: 1153222
Rhabdomyosarcomas of the female genital tract occurred only in children under 2 years, and those in the lower eyelid presented in the first year of life. A leiomyosarcoma-like appearance, and an undifferentiated small cell sarcoma sometimes mimicking Ewing's tumour, …
Rhabdomyosarcomas of the female genital tract occurred only in children under 2 years, and those in the lower eyelid presented in the first …
The value of adjuvant chemotherapy in the management of sarcomas in children.
Donaldson SS. Donaldson SS. Cancer. 1985 May 1;55(9 Suppl):2184-97. doi: 10.1002/1097-0142(19850501)55:9+<2184::aid-cncr2820551422>3.0.co;2-n. Cancer. 1985. PMID: 3884137 Review.
Sarcomas of childhood rank fifth in incidence of malignant tumors in children younger than 15 years. ...The remainder represent a heterogeneous group of diverse sarcomas which are not unique to children and include fibrosarcoma, synoviosarcoma, malignant f …
Sarcomas of childhood rank fifth in incidence of malignant tumors in children younger than 15 years. ...The remainder represen …
Neurofibromatosis type 1 and malignancy in childhood.
Varan A, Şen H, Aydın B, Yalçın B, Kutluk T, Akyüz C. Varan A, et al. Clin Genet. 2016 Mar;89(3):341-5. doi: 10.1111/cge.12625. Epub 2015 Jul 14. Clin Genet. 2016. PMID: 26073032
Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary neurocutaneous syndrome characterized by multi-system involvement and an increased incidence of both benign and malignant tumors. In this study, we evaluated the clinical presentation and prognosis of NF1 a …
Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary neurocutaneous syndrome characterized by multi-system involvement and an …
Intracranial mesenchymal tumors with FET-CREB fusion are composed of at least two epigenetic subgroups distinct from meningioma and extracranial sarcomas.
Sloan EA, Gupta R, Koelsche C, Chiang J, Villanueva-Meyer JE, Alexandrescu S, Eschbacher JM, Wang W, Mafra M, Ud Din N, Carr-Boyd E, Watson M, Punsoni M, Oviedo A, Gilani A, Kleinschmidt-DeMasters BK, Coss DJ, Lopes MB, Reddy A, Mueller S, Cho SJ, Horvai AE, Lee JC, Pekmezci M, Tihan T, Bollen AW, Rodriguez FJ, Ellison DW, Perry A, von Deimling A, Chang SM, Berger MS, Solomon DA. Sloan EA, et al. Brain Pathol. 2022 Jul;32(4):e13037. doi: 10.1111/bpa.13037. Epub 2021 Nov 25. Brain Pathol. 2022. PMID: 34821426 Free PMC article.
'Intracranial mesenchymal tumor, FET-CREB fusion-positive' occurs primarily in children and young adults and has previously been termed intracranial angiomatoid fibrous histiocytoma (AFH) or intracranial myxoid mesenchymal tumor (IMMT). ...These tumors resolved into …
'Intracranial mesenchymal tumor, FET-CREB fusion-positive' occurs primarily in children and young adults and has previously been termed intr …
Soft tissue tumours in childhood.
Malone M. Malone M. Histopathology. 1993 Sep;23(3):203-16. doi: 10.1111/j.1365-2559.1993.tb01192.x. Histopathology. 1993. PMID: 8225238 Review.
Congenital soft tissue tumours constitute a special group in which the clinical outcome may be particularly difficult to predict from the histological appearances. This review focuses on those malignant soft tumours which are either peculiar to childhood or which ma …
Congenital soft tissue tumours constitute a special group in which the clinical outcome may be particularly difficult to predict from the hi …
Soft tissue sarcomas of childhood: the differential diagnostic dilemma of the small blue cell.
Dehner LP. Dehner LP. Natl Cancer Inst Monogr. 1981 Apr;(56):43-59. Natl Cancer Inst Monogr. 1981. PMID: 6272117 Review.
The recently described small cell tumor of thoracopulmonary origin is likely a malignant neuroepithelial neoplasm. Hematopoietic tumors, such as non-Hodgkin's malignant lymphomas, granulocytic sarcoma, and malignant histiocytosis, may appear in the sof …
The recently described small cell tumor of thoracopulmonary origin is likely a malignant neuroepithelial neoplasm. Hematopoietic tumo …
27 results