Evidence map›Paper›PMID 42540718›Full record

ArticleInternational medical case reports journal2026

Orbital Compression Syndrome Mimicking Severe Malaria in a Child with Sickle Cell Disease in a Ugandan Refugee Settlement: A Case Report.

James Nelson Okema, Stephenson Ocen Oryem, Lydia Joyce Atto, Jude Ocen Okello, Jael Mary Nalukenge, Grace Acomo, Ronald Obal, Joel Atim Abong

Abstract readCase Reports
In one paragraph

Article in International medical case reports journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

James Nelson OkemaDepartment of Medicine, Faculty of Medicine, Gulu University, Gulu, Uganda.ORCID 0009-0001-6365-5018
Stephenson Ocen OryemDepartment of Medicine, Faculty of Medicine, Gulu University, Gulu, Uganda.
Lydia Joyce AttoDepartment of Medicine, Faculty of Medicine, Gulu University, Gulu, Uganda.
Jude Ocen OkelloDepartment of Medicine, Faculty of Medicine, Gulu University, Gulu, Uganda.
Jael Mary NalukengeDepartment of Medicine, Faculty of Medicine, Gulu University, Gulu, Uganda.
Grace AcomoDepartment of Paediatrics, St. Mary's Hospital Lacor, Gulu, Uganda.
Ronald ObalDepartment of Internal Medicine, St Mary's Hospital Lacor, Gulu, Uganda.ORCID 0009-0006-3772-7221
Joel Atim AbongDepartment of Clinical Services, Palabek Kal Health Centre IV, Lamwo District Local Government, Lamwo, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Orbital compression syndrome (OCS) is a rare, sight-threatening complication of sickle cell disease (SCD), caused by vaso-occlusive infarction of orbital bone marrow with subperiosteal hematoma formation. Its presentation overlaps with orbital cellulitis and severe malaria, creating diagnostic uncertainty in resource-limited humanitarian settings. Case Presentation: A 9-year-old boy with homozygous SCD (HbSS) presented to a primary health facility in Palabek Kal refugee settlement, Lamwo District, northern Uganda, with a 1-day history of sudden severe bilateral frontal headache radiating to the eyes, high-grade fever, and rapidly progressive bilateral periorbital edema, epiphora, and photophobia, without altered consciousness, seizures, vomiting, or respiratory distress. He was febrile (39.3°C) and unwell, with bilateral periorbital swelling, mild scleral icterus, and hepatomegaly (approximately 6 cm below the right costal margin); visual acuity, pupillary responses, extraocular movements, and proptosis assessment were normal. Laboratory evaluation showed severe anemia (hemoglobin 6.5 g/dL), leukocytosis (14.81 × 10 Management and Outcome: The child received intravenous artesunate, empirical broad-spectrum antibiotics, intravenous fluids, analgesics, and one unit of blood transfusion for severe anemia, with close ophthalmic monitoring. Fever resolved, periorbital swelling subsided, and visual function was preserved without surgical intervention. Conclusion: This case illustrates the diagnostic challenge of OCS in a child with SCD in a malaria-endemic humanitarian setting. OCS should be considered in any child with SCD presenting with acute bilateral periorbital swelling, headache, and fever, even when malaria is confirmed and orbital imaging is unavailable. Early recognition, parallel management of competing diagnoses, close clinical monitoring, and expanded access to orbital imaging in humanitarian settings are critical to prevent avoidable visual morbidity.

Indexed as

differential diagnosishumanitarian settingmalariaorbital compression syndromepediatricperiorbital swellingrefugee settlementsickle cell diseaseUganda

Identifiers

PMID42540718
PMCPMC13426365

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