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1. Full Text Smooth muscle tumors of soft tissue and non-uterine viscera: Biology and prognosis
by Miettinen, Markku
Modern Pathology, ISSN 0893-3952, 01/2014, Volume 27, Issue 1, pp. S17 - S19
Smooth muscle tumors are here considered an essentially dichotomous group composed of benign leiomyomas and malignant leiomyosarcomas. Soft tissue smooth... 
leiomyosarcoma | bone and soft tissue | leiomyoma | COL4A6 GENES | BENIGN METASTASIZING LEIOMYOMA | H-CALDESMON | PATHOLOGY | MESENCHYMAL TUMORS | EPITHELIAL MEMBRANE ANTIGEN | INFERIOR VENA-CAVA | LEIOMYOMATOSIS PERITONEALIS DISSEMINATA | GASTROINTESTINAL STROMAL TUMORS | CLINICOPATHOLOGICAL ANALYSIS | EPSTEIN-BARR-VIRUS | Neoplasms, Muscle Tissue - chemistry | Prognosis | Biomarkers, Tumor - analysis | Humans | Terminology as Topic | Leiomyoma - classification | Leiomyosarcoma - classification | Neoplasms, Muscle Tissue - genetics | Herpesvirus 4, Human - isolation & purification | Soft Tissue Neoplasms - virology | Soft Tissue Neoplasms - chemistry | Neoplasms, Muscle Tissue - classification | Hamartoma - classification | Soft Tissue Neoplasms - classification | Soft Tissue Neoplasms - pathology | Neoplasms, Muscle Tissue - virology | Biomarkers, Tumor - genetics | Cell Differentiation | Angiomyoma - classification | Soft Tissue Neoplasms - genetics | Neoplasms, Muscle Tissue - pathology
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2. Full Text Cellular angiofibroma: analysis of 25 cases emphasizing its relationship to spindle cell lipoma and mammary-type myofibroblastoma
by Flucke, U.E and Krieken, J.H. van and Mentzel, T
Modern Pathology, ISSN 0893-3952, 2011, Volume 24, Issue 1, pp. 82 - 89
Cellular angiofibroma represents a rare benign mesenchymal tumor, occurring mainly in the superficial soft tissue of the genital region. The involvement of... 
genital mesenchymal tumors | soft tissue | spindle cell lipoma | mammary-type myofibroblastoma | cellular angiofibroma | MESENCHYMAL TUMOR | ANGIOMYOFIBROBLASTOMA | FEMALE GENITAL-TRACT | SARCOMATOUS TRANSFORMATION | PATHOLOGY | SOFT-TISSUE | BENIGN NEOPLASM DISTINCT | SOLITARY FIBROUS TUMOR | AGGRESSIVE ANGIOMYXOMA | CLINICOPATHOLOGICAL ANALYSIS | SUPERFICIAL ANGIOMYXOMA | Antigens, CD34 - metabolism | Humans | Middle Aged | Lipoma - genetics | Angiofibroma - metabolism | Male | Lipoma - pathology | Breast Neoplasms - metabolism | Angiofibroma - genetics | Urogenital Neoplasms - metabolism | Vulvar Neoplasms - pathology | Neoplasms, Muscle Tissue - metabolism | Gene Deletion | Vulvar Neoplasms - metabolism | Aged, 80 and over | Biomarkers, Tumor - metabolism | Adult | Female | Lipoma - metabolism | DNA, Neoplasm - analysis | Soft Tissue Neoplasms - genetics | Neoplasms, Muscle Tissue - pathology | Retinoblastoma Protein - metabolism | Soft Tissue Neoplasms - metabolism | Urogenital Neoplasms - pathology | In Situ Hybridization, Fluorescence | Neoplasms, Muscle Tissue - genetics | Breast Neoplasms - genetics | Vulvar Neoplasms - genetics | Breast Neoplasms - pathology | Retinoblastoma Protein - genetics | Urogenital Neoplasms - genetics | Angiofibroma - pathology | Soft Tissue Neoplasms - pathology | Aged
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3. Full Text Mammary-type Myofibroblastoma: Clinicopathologic Characterization in a Series of 143 Cases
by Howitt, Brooke E and Fletcher, Christopher D.M
The American Journal of Surgical Pathology, ISSN 0147-5185, 03/2016, Volume 40, Issue 3, pp. 361 - 367
Mammary-type myofibroblastoma (MTMF) is a benign mesenchymal neoplasm initially described to occur in the breast. MTMF is typically CD34 and desmin positive... 
Mammary-type | Tumor | Soft tissue | Myofibroblastoma | SURGERY | MESENCHYMAL TUMOR | soft tissue | mammary-type | PROGNOSTIC NOMOGRAM | PATHOLOGY | BETA-CATENIN MUTATIONS | SOFT-TISSUE | SPINDLE-CELL LIPOMA | tumor | DESMOID-TYPE FIBROMATOSIS | GENE-EXPRESSION | myofibroblastoma | SOLITARY FIBROUS TUMOR | MALE BREAST | MORPHOLOGIC-SPECTRUM | Immunohistochemistry | Breast Neoplasms - surgery | Predictive Value of Tests | Neoplasms, Muscle Tissue - chemistry | Humans | Middle Aged | Child, Preschool | Male | Neoplasm, Residual | Young Adult | Breast Neoplasms - chemistry | Aged, 80 and over | Adult | Female | Child | Neoplasms, Muscle Tissue - pathology | Diagnosis, Differential | Biomarkers, Tumor - analysis | Neoplasm Recurrence, Local | Treatment Outcome | Tumor Burden | Biopsy | Breast Neoplasms - pathology | Neoplasms, Muscle Tissue - surgery | Adolescent | Aged
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4. Full Text Inflammatory myofibroblastic tumors harbor multiple potentially actionable Kinase fusions
by Lovly, Christine M and Gupta, Abha and Lipson, Doron and Otto, Geoff and Brennan, Tina and Chung, Catherine T and Borinstein, Scott C and Ross, Jeffrey S and Stephens, Philip J and Miller, Vincent A and Coffin, Cheryl M
Cancer Discovery, ISSN 2159-8274, 2014, Volume 4, Issue 8, pp. 889 - 895
Inflammatory myofibroblastic tumor (IMT) is a neoplasm that typically occurs in children. The genetic landscape of this tumor is incompletely understood and... 
ANAPLASTIC LYMPHOMA KINASE | CELL LUNG-CANCER | ALK | MYELOPROLIFERATIVE DISORDERS | ONCOLOGY | CRIZOTINIB | IDENTIFICATION | EXPRESSION | Inflammation - pathology | Proto-Oncogene Proteins - antagonists & inhibitors | Pyridines - administration & dosage | Humans | Neoplasms, Muscle Tissue - drug therapy | Male | Proto-Oncogene Proteins - genetics | Receptor, Platelet-Derived Growth Factor beta - genetics | Neoplasms, Muscle Tissue - genetics | Protein-Tyrosine Kinases - genetics | Pyrazoles - administration & dosage | Receptor Protein-Tyrosine Kinases - genetics | Inflammation - drug therapy | Oncogene Proteins, Fusion - genetics | Oncogene Proteins, Fusion - antagonists & inhibitors | Biomarkers, Tumor - genetics | Child | Neoplasms, Muscle Tissue - pathology | Protein-Tyrosine Kinases - antagonists & inhibitors | sarcoma | next generation sequencing | tyrosine kinase | Inflammatory myofibroblastic tumor | PDGFRβ | crizotinib | gene fusion | cancer | tyrosine kinase inhibitor | gene rearrangement | ROS1 | targeted therapeutics
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5. Full Text Mammary and vaginal myofibroblastomas are genetically related lesions: fluorescence in situ hybridization analysis shows deletion of 13q14 region
by Magro, Gaetano, MD, PhD and Righi, Alberto, MD and Casorzo, Laura, MD and Antonietta, Torrisi, MD and Salvatorelli, Lucia, MD and Kacerovská, Denisa, MD and Kazakov, Dmitry, MD and Michal, Michal, MD
Human Pathology, ISSN 0046-8177, 2012, Volume 43, Issue 11, pp. 1887 - 1893
Summary Partial monosomy 13q, a chromosomal alteration originally reported in spindle cell lipoma, has also been documented in a few cases of mammary... 
Pathology | Breast | FISH | Vagina | Myofibroblastoma | 13q14 deletion | MESENCHYMAL TUMOR | FEMALE GENITAL-TRACT | POTENTIAL DIAGNOSTIC PITFALL | ANGIOFIBROMA | PATHOLOGY | SOFT-TISSUE | SPINDLE-CELL LIPOMA | STROMA | SPECTRUM | SUPERFICIAL CERVICOVAGINAL MYOFIBROBLASTOMA | Chromosomes, Human, Pair 13 - genetics | Humans | Middle Aged | Lipoma - genetics | Angiofibroma - metabolism | Male | Lipoma - pathology | Genetic Loci | Breast Neoplasms - metabolism | Vaginal Neoplasms - genetics | Angiofibroma - genetics | Cell Nucleus - metabolism | Neoplasms, Muscle Tissue - metabolism | Cell Nucleus - pathology | Forkhead Transcription Factors - metabolism | Aged, 80 and over | Biomarkers, Tumor - metabolism | Female | Lipoma - metabolism | Neoplasms, Muscle Tissue - pathology | Vaginal Neoplasms - metabolism | Chromosome Deletion | Vaginal Neoplasms - pathology | In Situ Hybridization, Fluorescence | Forkhead Transcription Factors - genetics | Neoplasms, Muscle Tissue - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Angiofibroma - pathology | Aged | Forkhead Box Protein O1 | Fluorescence | Analysis | Smooth muscle | Genetic engineering | Reproductive system | Hybridization | Chromosomes
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6. Full Text Novel PAX3-NCOA1 Fusions in Biphenotypic Sinonasal Sarcoma With Focal Rhabdomyoblastic Differentiation
by Huang, Shih-Chiang and Ghossein, Ronald A and Bishop, Justin A and Zhang, Lei and Chen, Tse-Ching and Huang, Hsuan-Ying and Antonescu, Cristina R
The American Journal of Surgical Pathology, ISSN 0147-5185, 01/2016, Volume 40, Issue 1, pp. 51 - 59
Sarcomas arising in the sinonasal region are uncommon and encompass a wide variety of tumor types, including the newly described biphenotypic sinonasal sarcoma... 
low-grade sinonasal sarcoma with neural and myogenic features | NCOA1 | PAX3 | biphenotypic sinonasal sarcoma | MAML3 | SURGERY | MALIGNANT TRITON TUMOR | DIAGNOSIS | HEAD | PAX GENES | SPINDLE-CELL RHABDOMYOSARCOMA | PROGNOSTIC-FACTORS | NERVE SHEATH TUMOR | PATHOLOGY | SOFT-TISSUE | SOX10 | MYOGENIC FEATURES | Immunohistochemistry | Paired Box Transcription Factors - genetics | Paranasal Sinus Neoplasms - genetics | Predictive Value of Tests | Neoplasms, Muscle Tissue - chemistry | Cell Proliferation | Humans | Middle Aged | Male | SOXE Transcription Factors - analysis | Paranasal Sinus Neoplasms - chemistry | New York City | Nuclear Receptor Coactivator 1 - genetics | Adult | Female | Cell Differentiation | Sarcoma - genetics | Neoplasms, Muscle Tissue - pathology | Diagnosis, Differential | PAX3 Transcription Factor | Biomarkers, Tumor - analysis | Gene Fusion | In Situ Hybridization, Fluorescence | Reverse Transcriptase Polymerase Chain Reaction | Sarcoma - pathology | Neoplasms, Muscle Tissue - genetics | Sarcoma - chemistry | Paranasal Sinus Neoplasms - pathology | Phenotype | Taiwan | Aged | Biomarkers, Tumor - genetics
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7. Full Text Expression of ALK1 and p80 in inflammatory myofibroblastic tumor and its mesenchymal mimics: A study of 135 cases
by Cessna, Melissa H and Cessna, Melissa H and Zhou, Holly and Zhou, Holly and Sanger, Warren G and Sanger, Warren G and Perkins, Sherrie L and Perkins, Sherrie L and Tripp, Sheryl and Tripp, Sheryl and Pickering, Diane and Pickering, Diane and Daines, Clark and Daines, Clark and Coffin, Cheryl M and Coffin, Cheryl M
Modern Pathology, ISSN 0893-3952, 09/2002, Volume 15, Issue 9, pp. 931 - 938
Abnormalities of chromosome 2p23 with expression of ALK1 and p80 occur in both inflammatory myofibroblastic tumor (IMT) and anaplastic large cell lymphoma.... 
ALK gene rearrangements | Anaplastic large cell lymphoma | ALK immunohistochemistry | Inflammatory myofibroblastic tumor | DIAGNOSIS | P80(NPM/ALK) | inflammatory myofibroblastic tumor | INVOLVEMENT | 2P23 | PSEUDOTUMOR | LARGE-CELL LYMPHOMA | TPM3-ALK | PATHOLOGY | GENE | SARCOMAS | anaplastic large cell lymphoma | Immunohistochemistry | Humans | Rhabdomyosarcoma - metabolism | Leiomyosarcoma - metabolism | Rhabdomyosarcoma - pathology | Fibrosarcoma - metabolism | Activin Receptors, Type I - biosynthesis | Chromosomes, Human, Pair 2 - genetics | Protein-Tyrosine Kinases - genetics | Fibrosarcoma - pathology | Neoplasms, Muscle Tissue - metabolism | Nerve Sheath Neoplasms - pathology | Histiocytoma, Benign Fibrous - pathology | Leiomyosarcoma - genetics | Child | Soft Tissue Neoplasms - genetics | Neoplasms, Muscle Tissue - pathology | Histiocytoma, Benign Fibrous - genetics | Diagnosis, Differential | Nerve Sheath Neoplasms - genetics | Leiomyosarcoma - pathology | Histiocytoma, Benign Fibrous - metabolism | Carrier Proteins - biosynthesis | Soft Tissue Neoplasms - metabolism | In Situ Hybridization, Fluorescence | Myofibromatosis - metabolism | Nerve Sheath Neoplasms - metabolism | Fibroma - genetics | Myofibromatosis - genetics | Receptor Protein-Tyrosine Kinases | Fibroma - pathology | Bacterial Proteins | Neoplasms, Muscle Tissue - genetics | Fibrosarcoma - genetics | Membrane Proteins - biosynthesis | Activin Receptors, Type II | Fibroma - metabolism | Chromosome Aberrations | Soft Tissue Neoplasms - pathology | Mesoderm - metabolism | Rhabdomyosarcoma - genetics | Mesoderm - pathology | Myofibromatosis - pathology
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8. Full Text Inflammatory Myofibroblastic Tumor of the Uterus: Clinical and Pathologic Review of 10 Cases Including a Subset With Aggressive Clinical Course
by Parra-Herran, Carlos and Quick, Charles M and Howitt, Brooke E and Dal Cin, Paola and Quade, Bradley J and Nucci, Marisa R
The American Journal of Surgical Pathology, ISSN 0147-5185, 02/2015, Volume 39, Issue 2, pp. 157 - 168
Inflammatory myofibroblastic tumor is currently regarded as a neoplasm with intermediate biological potential and a wide anatomic distribution. Inflammatory... 
myxoid uterine tumors | inflammatory myofibroblastic tumor | anaplastic lymphoma kinase 1 | SURGERY | ALK-1 PROTEIN EXPRESSION | P80 | PSEUDOTUMOR | PATHOLOGY | REARRANGEMENTS | ANAPLASTIC LYMPHOMA KINASE | IMMUNOHISTOCHEMICAL FEATURES | GENE | SARCOMA | CRIZOTINIB | BLADDER | Immunohistochemistry | Uterine Neoplasms - genetics | Biomarkers, Tumor - analysis | Uterine Neoplasms - pathology | Humans | Middle Aged | In Situ Hybridization, Fluorescence | Neoplasms, Muscle Tissue - genetics | Receptor Protein-Tyrosine Kinases - genetics | Adult | Female | Aged | Retrospective Studies | Neoplasms, Muscle Tissue - pathology
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9. Full Text Nonepithelial Tumors and Tumor-like Lesions of the Skin and Subcutis in Children
by Dehner, Louis P and Gru, Alejandro A
Pediatric and Developmental Pathology, ISSN 1093-5266, 4/2018, Volume 21, Issue 2, pp. 150 - 207
This overview of mesenchymal tumors presenting in the skin and/or subcutis in children brings together the range of neoplasms and hamartomas which are seen in... 
giant cell fibroblastoma | neurofibroma | sarcoma | infantile hemangioma | myofibroma | GRANULAR-CELL TUMORS | NEUROFIBROMATOSIS TYPE-2 NF2 | VIRUS-ASSOCIATED LEIOMYOSARCOMA | PATHOLOGY | SOLITARY CIRCUMSCRIBED NEUROMA | SOFT-TISSUE TUMORS | ENDOVASCULAR PAPILLARY ANGIOENDOTHELIOMA | PALISADED ENCAPSULATED NEUROMA | PLEXIFORM FIBROHISTIOCYTIC TUMOR | PEDIATRICS | NERVE SHEATH TUMORS | DERMAL DENDROCYTE HAMARTOMA | Fibroma - diagnosis | Skin Neoplasms - pathology | Diagnosis, Differential | Soft Tissue Neoplasms - diagnosis | Humans | Nerve Sheath Neoplasms - diagnosis | Lipoma - pathology | Sarcoma - pathology | Vascular Neoplasms - diagnosis | Fibroma - pathology | Neoplasms, Muscle Tissue - diagnosis | Vascular Malformations - pathology | Nerve Sheath Neoplasms - pathology | Skin Neoplasms - diagnosis | Soft Tissue Neoplasms - pathology | Vascular Malformations - diagnosis | Vascular Neoplasms - pathology | Sarcoma - diagnosis | Lipoma - diagnosis | Child | Neoplasms, Muscle Tissue - pathology | Subcutaneous Tissue - pathology
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