Fibromatosis agresiva en hueco popliteo: A propósito de un caso [PDF]
, 1999 Se presenta un caso de una masa indolora en región posterior de la pierna en un varón de 35 años de crecimiento rápido, consistencia firme y mal delimitada.
Cima Suárez, M. de +2 more
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Contemporary Clinical Dentistry, 2018 Syndromes, especially if they occur early in the growth phase can be very debilitating and cause severe restriction of function. Juvenile hyaline fibromatosis is one such disorder. Our case report presents a girl child who was diagnosed with this debilitating condition.
Vikram Karande, Neelam Noel Andrade
openaire +3 more sources
Nodular Fasciitis of Neck in Childhood. [PDF]
, 2013 Nodular fasciitis, is a benign, pseudo sarcomatous proliferative lesion of the soft tissue, which is frequently misinterpreted as sarcoma, both clinically and microscopically.
Agarwal, N +6 more
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Pseudotumoural soft tissue lesions of the hand and wrist: a pictorial review [PDF]
, 2011 : Mimickers of soft tissue tumours in the hand and wrist are more frequent than true neoplastic lesions. Pseudotumours belong to a large and heterogeneous group of disorders, varying from normal anatomical variants, cystic lesions, post-traumatic lesions,
Filip M. Vanhoenacker +4 more
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Indian Journal of Dermatology, 2011 Juvenile hyaline fibromatosis is a rare, autosomal-recessive disease characterized by papular and nodular skin lesions, gingival hyperplasia, joint contractures and bone involvement in variable degrees. It is a connective tissue disorder with aberrant synthesis of glycosaminoglycans by fibroblasts.
Jayashree Krishnamurthy +3 more
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Fibromatosis extraabdominal agresiva: descripción de un caso y revisión de la literatura [PDF]
, 2009 El tumor desmoide es un raro tumor benigno de partes blandas, con gran capacidad invasiva local y sin potencial metastático. Se han descrito diversas variedades según su localización; siendo la variedad extraabdominal ó fibromatosis extraabdominal ...
Fernández Gabarda, Rafael +2 more
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Identification of heterogeneity among soft tissue sarcomas by gene expression profiles from different tumors [PDF]
, 2008 The heterogeneity that soft tissue sarcomas (STS) exhibit in their clinical behavior, even within histological subtypes, complicates patient care. Histological appearance is determined by gene expression.
Skubitz Amy PN +3 more
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Hyaline fibromatosis syndrome inducing mutations in the ectodomain of anthrax toxin receptor 2 can be rescued by proteasome inhibitors. [PDF]
, 2011 Hyaline Fibromatosis Syndrome (HFS) is a human genetic disease caused by mutations in the anthrax toxin receptor 2 (or cmg2) gene, which encodes a membrane protein thought to be involved in the homeostasis of the extracellular matrix.
Andrea Superti‐Furga +13 more
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Familial Infiltrative Fibromatosis (Desmoid Tumours) (MIM135290) Caused by a Recurrent 3′ APC Gene Mutation [PDF]
, 2017 Desmoid tumours are generally very rare but occur about 100 times more frequently in the colorectal cancer predisposition syndrome familial adenomatous polyposis (MIM 175100), being represented in about 10% of patients.
Evans, D. Gareth R. +5 more
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Aggressive fibromatosis of the head and neck: a new classification based on a literature review over 40 years (1968-2008) [PDF]
, 2010 BACKGROUND: Fibromatosis is an aggressive fibrous tumor of unknown etiology that is, in some cases, lethal. Until now, there has been no particular classification for the head and neck.
A Azzarelli +42 more
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