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BRIEF COMMUNICATION
Year : 2010  |  Volume : 58  |  Issue : 3  |  Page : 234-236

Spontaneous bilateral peripapillary, subhyaloid and vitreous hemorrhage with severe anemia secondary to idiopathic thrombocytopenic purpura


Smt. Kanuri Shanthamma Center for Retina Vitreous Diseases, L V Prasad Eye Institute, Kallam Anji Reddy Campus, Banjara Hills, Hyderabad-500 034, India

Correspondence Address:
Kapil Bhatia
Room no. 401, Smt. Kanuri Shanthamma Center for Retina Vitreous Diseases, L V Prasad Eye Institute, Kallam Anji Reddy Campus, Banjara Hills, Hyderabad-500034
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0301-4738.62651

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A 42-year-old female presented to us with a complaint of sudden painless loss of vision in both eyes of three days duration. Visual acuity was 20/100 for distance in both eyes. Fundus examination showed bilateral peripapillary hemorrhages, with subhyaloid and vitreous hemorrhage in both eyes. Hematological investigations revealed hemoglobin (HB 7 gm %) and severe thrombocytopenia (12,000/ ul). She was referred to a hematologist where a diagnosis of idiopathic thrombocytopenic purpura (ITP) was made. She was treated for systemic condition with regular ophthalmic follow-up. Over the next nine months, retinal hemorrhages completely resolved and the patient regained her visual acuity. The purpose of this case report is to highlight the clinical presentation of severe anemia, which is different from previous reports and the role of an ophthalmologist in first detecting the Idiopathic thrombocytopenic purpura (ITP), which led to successful recovery.


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