Fine needle aspiration cytology of the primitive myxoid mesenchymal tumor of infancy
Sign Up to like & getrecommendations! Published in 2022 at "Diagnostic Cytopathology"
DOI: 10.1002/dc.25046
Abstract: Primitive myxoid mesenchymal tumor of infancy (PMMTI) is a recently described entity, previously included under the umbrella of undifferentiated sarcomas. These tumors are notorious for recurrence, chemoresistance and may even metastasize. We describe here, for… read more here.
Keywords: primitive myxoid; cytology; tumor infancy; mesenchymal tumor ... See more keywords
Phosphaturic Mesenchymal Tumor in the Maxillofacial Region: A Diagnostic Dilemma
Sign Up to like & getrecommendations! Published in 2021 at "Journal of Maxillofacial and Oral Surgery"
DOI: 10.1007/s12663-020-01496-8
Abstract: Oncogenic osteomalacia is a rare paraneoplastic syndrome and is associated with the presence of phosphaturic mesenchymal tumor (PMT) which results in renal phosphate wasting with hypophosphatemia. In total, 95% of cases reported in upper and… read more here.
Keywords: maxillofacial region; region diagnostic; phosphaturic mesenchymal; tumor ... See more keywords
PHOSPHATURIC MESENCHYMAL TUMOR IN THE MANDIBLE WITH ASSOCIATED ONCOGENIC OSTEOMALACIA: A CASE REPORT
Sign Up to like & getrecommendations! Published in 2019 at "Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology"
DOI: 10.1016/j.oooo.2019.02.154
Abstract: Phosphaturic mesenchymal tumor (PMT) is a rare neoplasm that has been associated with oncogenic osteomalacia. This tumor secretes fibroblast growth factor-23 (FGF-23). Although other mesenchymal tumors can cause oncogenic osteomalacia, PMT is the most common… read more here.
Keywords: phosphaturic mesenchymal; tumor; oncogenic osteomalacia; mesenchymal tumor ... See more keywords
Phosphaturic mesenchymal tumor with an admixture of epithelial and mesenchymal elements in the jaws: clinicopathological and immunohistochemical analysis of 22 cases with literature review
Sign Up to like & getrecommendations! Published in 2018 at "Modern Pathology"
DOI: 10.1038/s41379-018-0100-0
Abstract: Information on the heterogeneity of phosphaturic mesenchymal tumor, a rare entity associated with tumor-induced osteomalacia, is limited. In this retrospective analysis of 222 phosphaturic mesenchymal tumors, 22 cases exhibited mixed mesenchymal and epithelial elements, which… read more here.
Keywords: tumor mixed; connective tissue; phosphaturic mesenchymal; mesenchymal tumor ... See more keywords
Malignant phosphaturic mesenchymal tumor with pulmonary metastasis
Sign Up to like & getrecommendations! Published in 2017 at "Medicine"
DOI: 10.1097/md.0000000000006750
Abstract: Rationale: Phosphaturic mesenchymal tumor (PMT) is a new tumor entity of soft tissue and bone tumor recently accepted by the World Health Organization, which typically causes the paraneoplastic syndrome of tumor-induced osteomalacia (TIO). The majority… read more here.
Keywords: recurrence; metastasis; pulmonary metastasis; phosphaturic mesenchymal ... See more keywords
Primitive Myxoid Mesenchymal Tumor of Infancy With Fatal Hemorrhage In Utero: A Case Report and Literature Review.
Sign Up to like & getrecommendations! Published in 2022 at "Journal of pediatric hematology/oncology"
DOI: 10.1097/mph.0000000000002474
Abstract: Primitive myxoid mesenchymal tumor of infancy (PMMTI) is a rare soft tissue sarcoma in childhood. We present the case of a newborn male who experienced a severe hemorrhage in utero from the tumor on the… read more here.
Keywords: hemorrhage; mesenchymal tumor; primitive myxoid; case ... See more keywords
Brain parenchymal angiomatoid fibrous histiocytoma and spinal myxoid mesenchymal tumor with FET: CREB fusion, a spectrum of the same tumor type
Sign Up to like & getrecommendations! Published in 2022 at "Neuropathology"
DOI: 10.1111/neup.12814
Abstract: Angiomatoid fibrous histiocytomas (AFH) is a rare soft tissue tumor of intermediate malignant potential, and its histology is diverse. It can occur in several organs including intracranial and soft tissues. Here, we report two cases… read more here.
Keywords: myxoid; brain parenchymal; mesenchymal tumor; fet creb ... See more keywords
Peptide Receptor Radionuclide Therapy for a Phosphaturic Mesenchymal Tumor
Sign Up to like & getrecommendations! Published in 2020 at "Case Reports in Oncology"
DOI: 10.1159/000510334
Abstract: Tumor-induced osteomalacia is a very rare paraneoplastic syndrome. It can be caused by phosphaturic mesenchymal tumor (PMT), a generally benign tumor that produces fibroblast growth factor 23 (FGF-23), which can cause a severe renal phosphate… read more here.
Keywords: phosphaturic mesenchymal; receptor radionuclide; radionuclide therapy; peptide receptor ... See more keywords
Mesenchymal tumor organoid models recapitulate rhabdomyosarcoma subtypes
Sign Up to like & getrecommendations! Published in 2022 at "EMBO Molecular Medicine"
DOI: 10.15252/emmm.202216001
Abstract: Rhabdomyosarcomas (RMS) are mesenchyme-derived tumors and the most common childhood soft tissue sarcomas. Treatment is intense, with a nevertheless poor prognosis for high-risk patients. Discovery of new therapies would benefit from additional preclinical models. Here… read more here.
Keywords: organoid models; models recapitulate; recapitulate rhabdomyosarcoma; tumor organoid ... See more keywords
Phosphaturic Mesenchymal Tumor
Sign Up to like & getrecommendations! Published in 2022 at "American Journal of Neuroradiology"
DOI: 10.32388/kmb14z
Abstract: Phosphaturic mesenchymal tumors (PMTs) are neoplasms associated with tumor-induced osteomalacia. Patients typically present with pathologic fractures in the setting of chronic hypophosphatemic hyperphosphaturic osteomalacia, as well as gradual muscle weakness, bone pain, and difficulty walking.… read more here.
Keywords: symptomatology; phosphaturic mesenchymal; tumor; mesenchymal tumors ... See more keywords
Fibroblast Growth Factor 23-Producing Phosphaturic Mesenchymal Tumor with Extraordinary Morphology Causing Oncogenic Osteomalacia
Sign Up to like & getrecommendations! Published in 2020 at "Medicina"
DOI: 10.3390/medicina56010034
Abstract: A possible cause of hypophosphatemia is paraneoplastic secretion of fibroblast growth factor 23 (FGF-23). Tumors secreting FGF-23 are rare, mostly of mesenchymal origin, usually benign, and may be located anywhere in the body, including hands… read more here.
Keywords: fgf; fibroblast growth; growth factor; phosphaturic mesenchymal ... See more keywords