Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA, USA.
National and Kapodistrian University of Athens, Athens, Greece.
Ocul Immunol Inflamm. 2022 May 19;30(4):978-980. doi: 10.1080/09273948.2020.1828491. Epub 2020 Oct 13.
To describe a case of paraneoplastic pemphigus (PNP) presenting as spontaneous bilateral corneal perforations in a patient with follicular dendritic cell sarcoma.
Retrospective chart reviewResults: A 73-year-old Greek woman with a history of follicular dendritic cell sarcoma (FDCS) presented with bilateral corneal perforations and a cicatrizing conjunctivitis. Her diagnosis was consistent with PNP with corneal and conjunctival involvement after a change in her chemotherapy regimen from intravenous cyclophosphamide to gemcitabine. She was treated with a multilayered amniotic membrane in the right eye and cyanoacrylate glue in the left eye. Systemic intravenous cyclophosphamide and oral prednisone were re-started. Both perforations healed but the patient passed away soon after precluding further follow-up.
Ocular manifestations of PNP can rarely present with spontaneous corneal perforations. This is the first case of FDCS-associated PNP with corneal involvement. Such cases should be diagnosed expediently and managed with aggressive systemic immunosuppressive therapy.
描述一例副肿瘤天疱疮(PNP)病例,患者患有滤泡树突状细胞肉瘤,表现为自发性双侧角膜穿孔。
回顾性病历分析
一名 73 岁的希腊女性,患有滤泡树突状细胞肉瘤(FDCS)病史,出现双侧角膜穿孔和瘢痕性结膜炎。在化疗方案从静脉注射环磷酰胺改为吉西他滨后,她被诊断为 PNP,伴角膜和结膜受累。在右眼行多层羊膜移植,左眼行氰基丙烯酸酯胶封闭。重新开始全身静脉注射环磷酰胺和口服泼尼松龙。两个穿孔均愈合,但患者在随访前不久去世,无法进一步随访。
PNP 的眼部表现罕见地表现为自发性角膜穿孔。这是首例 FDCS 相关 PNP 伴角膜受累的病例。此类病例应迅速诊断,并采用积极的全身免疫抑制治疗。