Wan-Wei Loo, Tengku-Norina Tuan-Jaffar, Azma-Azalina Ahmad-Alwi, Zulkifli Abdul-Ghani, Zunaina Embong
Department of Ophthalmology, Hospital Raja Perempuan Zainab II, Kota Bharu ; Department of Ophthalmology, School of Medical Sciences, Health Campus, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
Department of Ophthalmology, Hospital Raja Perempuan Zainab II, Kota Bharu.
Int Med Case Rep J. 2014 Jan 24;7:15-7. doi: 10.2147/IMCRJ.S55017. eCollection 2014.
A 45-year-old female with underlying idiopathic thrombocytopenic purpura (ITP) complained of acute onset of reduced vision and floaters, in both eyes, for 3 weeks. Visual acuity was 6/36 and 6/60 in the right eye and left eye, respectively. Ophthalmoscopy showed bilateral peripapillary, subhyaloid and vitreous hemorrhage. Hematological evaluation revealed moderate anemia (hemoglobin: 93 g/L) and mild thrombocytopenia (platelets: 120×10(9)/L). She was co-managed by a hematologist and ophthalmologists; she was treated medically. Follow-up care during the next 6 weeks revealed spontaneous, partially resolving hemorrhage, with improvement of visual acuity. The purpose of this case report is to highlight ophthalmic involvement of ITP in this patient, despite her only-mild thrombocytopenia, and her spontaneous recovery, despite her receiving only medical treatment.
一名45岁患有特发性血小板减少性紫癜(ITP)的女性,主诉双眼视力下降和出现飞蚊症3周,起病急。右眼视力为6/36,左眼视力为6/60。眼底镜检查显示双侧视乳头周围、玻璃膜下和玻璃体出血。血液学评估显示中度贫血(血红蛋白:93 g/L)和轻度血小板减少(血小板:120×10⁹/L)。她由血液科医生和眼科医生共同管理;接受了药物治疗。在接下来6周的随访中,出血自发部分吸收,视力有所改善。本病例报告的目的是强调该患者尽管仅有轻度血小板减少,但仍出现了ITP的眼部受累情况,并且尽管仅接受了药物治疗,仍实现了自发恢复。