Kamal Saurabh, Goel Ruchi, Bodh Sonam Angmo
Guru Nanak Eye Centre, Ophthalmic Plastic Surgery Services, Maulana Azad Medical College, New Delhi, India.
Middle East Afr J Ophthalmol. 2012 Oct;19(4):426-8. doi: 10.4103/0974-9233.102767.
Amyloidosis and its ophthalmic manifestations are rare. The unusual presentation can result in diagnostic delay and increase ocular morbidity. Additionally, there are various predisposing conditions and systemic involvement can affect various organs. Hence, localized disease warrants a thorough clinical evaluation and laboratory investigation. We report two cases of primary localized amyloidosis presenting as a tarsal mass and ptosis. The diagnosis was established on histopathology. There were no predisposing conditions and no systemic involvement. The disease was probably related to the local immunocyte disorder.
淀粉样变性及其眼部表现较为罕见。这种不寻常的表现可能导致诊断延迟并增加眼部发病率。此外,存在多种诱发因素,且系统性受累可影响多个器官。因此,局限性疾病需要进行全面的临床评估和实验室检查。我们报告了两例表现为睑板肿块和上睑下垂的原发性局限性淀粉样变性病例。诊断通过组织病理学确定。不存在诱发因素且无系统性受累。该疾病可能与局部免疫细胞紊乱有关。