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JAAD Case Reports, ISSN 2352-5126, 03/2018, Volume 4, Issue 2, pp. 185 - 188
A 14-month-old boy presented with a slow-growing, asymptomatic back plaque, which was biopsied and found to have S100 positivity, sparse CD34 staining, and no... 
lipofibromatosis-like neural tumor | infantile mesenchymal tumor | pediatric skin tumor
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 10/2019, Volume 43, Issue 10, pp. 1384 - 1391
A major breakthrough in the classification of soft tissue tumors has been the recent identification of NTRK-fusion related neoplasms which are amenable to... 
RET | fusion | SURGERY | lipofibromatosis-like neural tumor | CARCINOMAS | NTRK | PATHOLOGY | REARRANGEMENTS | infantile fibrosarcoma | SUBSET | Sarcoma | Physiological aspects | Protein tyrosine kinase | Genetic aspects | Health aspects | Gene fusion | Proto-oncogenes
Journal Article
Philippine Journal of Otolaryngology Head and Neck Surgery, ISSN 1908-4889, 06/2011, Volume 26, Issue 1
Objective: To describe a rare case of lipofibromatosis presenting as a head and neck mass in a 6-year-old child.   Method: Design: Case Report Setting:... 
lipofibromatosis
Journal Article
Annales de Dermatologie et de Venereologie, ISSN 0151-9638, 05/2011, Volume 138, Issue 5, pp. 391 - 394
Background: Lipofibromatosis is a recently classified form of benign tumor in children; it is of non-specific clinical presentation and is seen mainly on the... 
Lipofibromatosis | Tumor | Child | Hand | Fibromatosis
Journal Article
Seminars in Diagnostic Pathology, ISSN 0740-2570, 03/2019, Volume 36, Issue 2, pp. 95 - 104
Journal Article
Journal of Pediatric Surgery, ISSN 0022-3468, 2012, Volume 47, Issue 5, pp. 1028 - 1031
Abstract Lipofibromatosis is a rare benign fibrofatty tumor of childhood. The typical presentation of this tumor is as a poorly demarcated and slow-growing... 
Pediatrics | Surgery | MRI | Lipofibromatosis | SURGERY | PEDIATRICS | TISSUE | Fibroma - diagnosis | Knee | Soft Tissue Neoplasms - diagnosis | Humans | Infant | Male | Lipoma - diagnosis
Journal Article
Case Reports in Oncology, ISSN 1662-6575, 03/2018, Volume 11, Issue 1, pp. 179 - 184
A 5-year-old girl presented with a big painless mass, sized 24 × 37 × 35 cm, in her lower left limb. MRI revealed a huge heterogeneous mass splaying from the... 
Case Report | Lipofibromatosis | Limb salvage | Amputation | Musculoskeletal system | Pediatrics | Histopathology | Nuclear magnetic resonance--NMR | Gait | Anemia | Surgery | Bones | Tumors
Journal Article
F1000Research, ISSN 2046-1402, 2018, Volume 7, p. 1963
Fibroblastic and myofibroblastic tumors comprise a morphologically diverse and biologically variable group of neoplasms that affect a wide age range. Specific... 
Lipofibromatosis | Fibrous hamartoma of infancy | Infantile fibrosarcoma | Infantile myofibromatosis | Primitive myxoid mesenchymal tumor of infancy | Spindle cell rhabdomyosarcoma | Pathology | Mesenchyme | Morphology | Rhabdomyosarcoma | Fibrosarcoma | Infants | Differential diagnosis | Dermatofibrosarcoma protuberans | Children | Mutation | Neoplasia | Tumors
Journal Article
AMERICAN JOURNAL OF DERMATOPATHOLOGY, ISSN 0193-1091, 04/2010, Volume 32, Issue 2, pp. 198 - 199
Journal Article
AMERICAN JOURNAL OF DERMATOPATHOLOGY, ISSN 0193-1091, 04/2010, Volume 32, Issue 2, pp. 170 - 170
Journal Article
Journal Article
Bone Reports, ISSN 2352-1872, 12/2016, Volume 5, pp. 292 - 298
Neurofibromatosis type 1 (NF1) is a commonly occurring genetic disorder in children. Mutation in the NF1 gene has its implication in poor osteoblastic... 
Lipofibromatosis | Pamidronate | Bone formation | Congenital pseudarthrosis tibia | Differentiation | Mesenchymal stem cells
Journal Article
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