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CASE REPORT article

Front. Oncol.
Sec. Neuro-Oncology and Neurosurgical Oncology
Volume 14 - 2024 | doi: 10.3389/fonc.2024.1456960

Orbital Granular Cell Tumor Involving the Superior Rectus Muscle: A Case Report

Provisionally accepted
  • 1 Chongqing Aier Eye Hospital, Chongqing, Chongqing Municipality, China
  • 2 Central South University, Changsha, Hunan Province, China
  • 3 Chongqing Emergency Medical Center, Chongqing, China

The final, formatted version of the article will be published soon.

    Objective:To assess the clinicopathological characteristics and differential diagnosis of orbital granular cell tumor (GCT).Methods:Clinical and imaging data of a rare case of orbital granular cell tumor involving the superior rectus muscle were collected.Its clinical characteristics,imaging,and histopathological features were observed.Results:A 36-year-old female patient presented with a 2-year history of left eye proptosis.Magnetic resonance imaging (MRI) enhancement suggested a space-occupying lesion in the left superior rectus muscle region.On T1-weighted and T2-weighted MRI,the tumor was isointense to gray matter and significantly enhanced on the enhanced scan.Microscopic examination revealed that most tumor cells exhibited diffuse growth with unclear boundaries,and some cells were arranged in small nests.The tumor cells were large,with abundant,coarse eosinophilic granules in the cytoplasm.Occasional cells contained larger round eosinophilic droplets in the cytoplasm.Focal areas showed foamy cells,small and central round or oval nuclei with occasional nuclear enlargement and mild atypia,inconspicuous nucleoli,rare mitoses,and low proliferative activity.Immunohistochemistry results were:Vimentin (+),S-100 (+),CD68 (+),Ki67 (2%+),Inhibin-a (-),CK (-),SMA (-),Desmin (-).The pathological examination of a specimen harvested from the mass corresponded to a granular cell tumor.:Orbital granular cell tumor is rare and should be considered in the differential diagnosis of orbital tumors.It is essential to distinguish it from thyroid-associated ophthalmopathy,inflammatory pseudotumor,and myohemangioma.Definitive diagnosis requires a comprehensive analysis of clinical,histopathological,and immunohistochemical findings.Surgical excision is the primary treatment for orbital granular cell tumors.For patients with incomplete tumor resection,close follow-up is necessary.Proton beam radiation therapy can be considered to prevent recurrence or metastasis if needed.

    Keywords: Orbital tumor, Granular Cell Tumor, Superior rectus muscle, Immunohistochemistry, Clinicopathological characteristics

    Received: 24 Jul 2024; Accepted: 11 Oct 2024.

    Copyright: © 2024 Wang, Han, Peng, Li and Yuan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Hongfeng Yuan, Chongqing Aier Eye Hospital, Chongqing, 400020, Chongqing Municipality, China

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