Sabol Rachel A, Bubenzer Virginia, Moroz Krzysztof, Halat Shams, Dang Audrey, Ferdinand Keith, Traylor Angela, Boyd Carol, Harris Kendra
Tulane University School of Medicine, New Orleans, LA, USA.
Department of Radiation Oncology, Tulane University School of Medicine, New Orleans, LA, USA.
Case Rep Ophthalmol Med. 2020 Sep 5;2020:8873078. doi: 10.1155/2020/8873078. eCollection 2020.
IgG4-related ophthalmic disease is a rare, newly recognized entity with high failure rates on first-line therapy of systemic corticosteroids and no other proven management options. Here, we present the clinical course of a patient with IgG4 ophthalmic disease who achieved a favorable response from radiotherapy. Our patient initially presented with a history of recurrent painful flares of orbital inflammation, a pathologic diagnosis follicular lymphoid hyperplasia from a right lacrimal gland biopsy, and MRI imaging noting expansion of the lateral rectus muscle of the right eye. Initial treatment with dacryoadenectomy and multiple courses of corticosteroids failed to keep his symptoms at bay. Further evaluation revealed florid IgG4 staining. In this context, he was evaluated for image-guided intensity-modulated radiotherapy (IG-IMRT) to the orbit to 20 Gy in 10 fractions. His ophthalmic symptoms resolved.
This treatment experience suggests radiotherapy may be a favorable option for symptom relief in patients with IgG4-related ophthalmic disease not controlled by corticosteroids.
IgG4相关性眼病是一种罕见的、新认识的疾病实体,一线全身糖皮质激素治疗失败率高,且没有其他经证实的治疗选择。在此,我们报告1例IgG4眼病患者的临床病程,该患者接受放射治疗后取得了良好疗效。我们的患者最初表现为眼眶炎症反复疼痛发作史,右侧泪腺活检病理诊断为滤泡性淋巴组织增生,MRI成像显示右眼外直肌增粗。泪腺切除术及多疗程糖皮质激素初始治疗未能控制其症状。进一步评估显示IgG4染色呈阳性。在此情况下,对其进行了眼眶图像引导调强放射治疗(IG-IMRT),分10次给予20 Gy剂量。其眼部症状得以缓解。
该治疗经验表明,对于糖皮质激素治疗无法控制的IgG4相关性眼病患者,放射治疗可能是缓解症状的良好选择。