Primary pulmonary epithelioid inflammatory myofibroblastic sarcoma: a rare entity and a literature review
Journal of Pathology and Translational Medicine. 2022;56(4):231-237 
Pulmonary epithelioid inflammatory myofibroblastic sarcoma with multiple bone metastases: case report and review of literature
Diagnostic Pathology. 2015;10(1):
Misdiagnosis of inflammatory myofibroblastic tumor as primary pulmonary myxoid sarcoma: A case report
. 2022;
A Case Report of RRBP1-ALK Fusion Gene-Positive Epithelioid Inflammatory Myofibroblastic Sarcoma With Collagenous Stroma
. 2021;
Primary epithelioid sarcoma of the oral cavity: Review of literature and presentation of a rare entity
Oral Surgery. 2021;
‘ALK oncoproteins in atypical inflammatory myofibroblastic tumours: novel RRBP1-ALK fusions in epithelioid inflammatory myofibroblastic sarcoma’
The Journal of Pathology. 2017;242(2):260-260
Primary, Dural-Based, Ewing Sarcoma in a Pediatric Patient: Presentation of a Rare Tumor Entity with Literature Review
. 2022;
Epithelioid inflammatory myofibroblastic sarcoma with VCL–ALK fusion of central nervous system: case report and brief review of the literature
Brain Tumor Pathology. 2021;39(1):35-42
Correction to: Epithelioid inflammatory myofibroblastic sarcoma with VCL–ALK fusion of central nervous system: case report and brief review of the literature
Brain Tumor Pathology. 2022;39(1):43-43
RARE-23. PRIMARY INTRA-AXIAL CENTRAL NERVOUS SYSTEM INFLAMMATORY MYOFIBROBLASTIC TUMOR, ALK NEGATIVE: A RARE ENTITY
Neuro-Oncology. 2018;20(suppl_6):vi241-vi241