Panophthalmitis in a case of Glanzmann thrombasthenia – The dilemma in diagnosis

We present a rare case of a middle-aged female diagnosed with Glanzmann Thrombasthenia who developed panophthalmitis following platelet transfusion. The patient presented with acute vision loss, proptosis, and ocular pain in the right eye following a platelet transfusion. Imaging confirmed panophthalmitis, while cultures were inconclusive. The patient was treated with intravenous and fortified topical antibiotics along with platelet transfusions. Despite aggressive management, the right eye progressed to phthisis bulbi. Systemic infection was controlled, and ocular pain and swelling significantly reduced. The patient was managed with systemic and fortified topical antibiotics under the care of a multidisciplinary team, including ophthalmologists, hematologists, and infectious disease specialists. This report highlights the diagnostic challenges, management dilemmas, and the importance of an interdisciplinary approach in managing infectious complications in patients with inherited platelet function disorders.

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Publication Details

Journal
Romanian Journal of Ophthalmology
Published
2025-09-15
DOI
https://doi.org/10.22336/rjo.2025.65
Primary Topic
Ocular Diseases and Behçet’s Syndrome
Type
article
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article

Panophthalmitis in a case of Glanzmann thrombasthenia – The dilemma in diagnosis

Thanuja Gopal Pradeep, Sandeep Sreerama Reddy, Lahari Velivelli, Rashmi Palassery
Romanian Journal of Ophthalmology
Ocular Diseases and Behçet’s Syndrome
article

Panophthalmitis in a case of Glanzmann thrombasthenia – The dilemma in diagnosis

Thanuja Gopal Pradeep, Sandeep Sreerama Reddy, Lahari Velivelli, Rashmi Palassery
article en

Abstract

We present a rare case of a middle-aged female diagnosed with Glanzmann Thrombasthenia who developed panophthalmitis following platelet transfusion. The patient presented with acute vision loss, proptosis, and ocular pain in the right eye following a platelet transfusion. Imaging confirmed panophthalmitis, while cultures were inconclusive. The patient was treated with intravenous and fortified topical antibiotics along with platelet transfusions. Despite aggressive management, the right eye progressed to phthisis bulbi. Systemic infection was controlled, and ocular pain and swelling significantly reduced. The patient was managed with systemic and fortified topical antibiotics under the care of a multidisciplinary team, including ophthalmologists, hematologists, and infectious disease specialists. This report highlights the diagnostic challenges, management dilemmas, and the importance of an interdisciplinary approach in managing infectious complications in patients with inherited platelet function disorders.

Romanian Journal of OphthalmologyVol. 69(3)
M S Ramaiah University of Applied Sciences (IN), M.S. Ramaiah Medical College (IN)
Openalex Percentile: Top 57%
Ocular Diseases and Behçet’s Syndrome
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Panophthalmitis in a case of Glanzmann thrombasthenia – The dilemma in diagnosis — Thanuja Gopal Pradeep, Sandeep Sreerama Reddy, et al. · Romanian Journal of Ophthalmology (2025) | TGRS Research Map | TGRS