Inflammatory myofibroblastic tumor from molecular diagnostics to current treatment

P Chmiel, A Słowikowska, Ł Banaszek… - Oncology …, 2024 - pmc.ncbi.nlm.nih.gov
Inflammatory myofibroblastic tumor (IMT) is a rare neoplasm with intermediate malignancy
characterized by a propensity for recurrence but a low metastatic rate. Diagnostic challenges …

Recurrent Inflammatory Myofibroblastic Tumor of Larynx Harboring a Novel THBS1:: ALK Fusion

N Ajmal, SM Gargano, U Gosavi… - International Journal of …, 2024 - Wiley Online Library
Inflammatory myofibroblastic tumor (IMT) is a rare soft tissue tumor primarily occurring in the
abdominopelvic region of young patients, and it is characterized by spindle‐shaped …

NTRK Fusions in 1113 Solid Tumors in a Single Institution

H Bang, MS Lee, M Sung, J Choi, S An, SH Kim… - Diagnostics, 2022 - mdpi.com
Simple Summary Recently, there has been increasing interest in identifying NTRK fusions in
various tumors, as they are therapeutically targetable driver mutations. In tumor types with …

Inflammatory myofibroblastic tumor 12 years after treatment for synovial sarcoma: a case report

A Shah, E Pey, JU Achonu, JDK Bai… - Orthopedic Research and …, 2021 - Taylor & Francis
Inflammatory myofibroblastic tumors (IMTs) are mesenchymal neoplasms most seen in the
abdominopelvic region, lung, and retroperitoneum; and less commonly seen in virtually any …

[HTML][HTML] Inflammatory Myofibroblastic Tumor: A Rare Case Report

ND Luke, S Gottlieb, J Brothers, S Winikoff - Cureus, 2023 - ncbi.nlm.nih.gov
Inflammatory myofibroblastic tumors (IMTs) are rare benign tumors that can occur anywhere
in the body, most commonly in the pediatric and young adult populations. The gold standard …

[HTML][HTML] Successful management of an unusual case of pediatric inflammatory myofibroblastic tumor: a case report and literature review

AM Amro, T Almassri, M Albandak… - Annals of Medicine …, 2025 - journals.lww.com
Conclusion: IMTs require individualized treatment approaches based on the location and
extent of the tumor. Long-term follow-up is essential for monitoring recurrence and …

A Rare Case of Inflammatory Myofibroblastic Tumor Mimicking Fibrous Adhesions Resulting in Bowel Obstruction

S Washburn, R Jessica Thomas… - Case Reports in …, 2024 - Wiley Online Library
Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal tumors of unknown etiology
composed of myofibroblastic cells admixed with inflammatory cells. Presented is a 72‐year …

肝脏炎性肌纤维母细胞瘤的临床特点及治疗策略

高远, 俞鹏, 曹李 - 肝胆胰外科杂志, 2023 - gdy.qk.wmu.edu.cn
目的探讨肝脏炎性肌纤维母细胞瘤(HIMT) 的临床特点及治疗方法. 方法回顾性分析中国人民
解放军总医院第五医学中心2011 年1 月到2022 年11 月诊治的15 例HIMT 患者的临床资料 …

[HTML][HTML] Urachal inflammatory myofibroblastic tumor with FN1:: ALK fusion: A case report and literature review

N Tara, S Mehta, PP Trivedi, K Patel, T Trivedi - Urology Case Reports, 2024 - Elsevier
Urachal tumors are rare and comprise of both benign and malignant neoplasms. Epithelial
origin tumors are more common than mesenchymal origin tumors. We report a case Urachal …

ALK-Negative Inflammatory Myofibroblastic Tumor: A Challenging Case in a Premature Newborn

C Regaieg, M Triki, T Cheikrouhou… - Journal of Neonatal …, 2023 - content.iospress.com
Inflammatory myofibroblastic tumors (IMT) are rare borderline tumors with a variable
histological appearance that may mimic multiple mesenchymal tumors. We present a rare …