Clinical features and prognosis of orbital inflammatory myofibroblastic tumor
Orbital IMT is a locally invasive disease that may recur or lead to sarcomatoid degeneration, primarily affecting young and middle-aged patients. The presence of lymphadenopathy and a Ki-67 index of 10% or higher may signify a poor prognosis.
Authors
- Ting-Ting Ren (ORCID: https://orcid.org/0000-0002-1108-7450)
- Hongwei Yan (ORCID: https://orcid.org/0000-0002-4412-6217)
- Sha Zhao (ORCID: https://orcid.org/0000-0002-4298-228X)
- Jing Li (ORCID: https://orcid.org/0000-0003-4602-3227)
- Bin Zhang (ORCID: https://orcid.org/0000-0002-2970-746X)
- Rui Liu (ORCID: https://orcid.org/0000-0003-2610-1144)
- Jianmin Ma (ORCID: https://orcid.org/0000-0003-2081-2877)
- Hong Zhang (ORCID: https://orcid.org/0000-0002-5866-4235)
- Qi-Han Guo
- Nan Wang (ORCID: https://orcid.org/0000-0002-8842-3424)
- Yufei Zhang (ORCID: https://orcid.org/0009-0009-3863-204X)
Institutions
- Beijing Tongren Hospital (CN)
- Jinan Maternity And Care Hospital (CN)
- Shandong Maternal and Child Health Hospital (CN)
Publication Details
- Journal
- International Journal of Ophthalmology
- Published
- 2025-12-17
- DOI
- https://doi.org/10.18240/ijo.2026.01.14
- Citations
- 1
- Primary Topic
- IgG4-Related and Inflammatory Diseases
- Type
- article
- Field-Weighted Citation Impact
- 1.67