Subperiosteal Orbital Hematoma: A Rare Clinical Manifestation of Sickle Cell Disease - A Case Report.

التفاصيل البيبلوغرافية
العنوان: Subperiosteal Orbital Hematoma: A Rare Clinical Manifestation of Sickle Cell Disease - A Case Report.
المؤلفون: Hanna NG; Department of Surgery, Division of Ophthalmology, McMaster University, Hamilton, ON, Canada., Musleh A; Department of Surgery, Division of Ophthalmology, McMaster University, Hamilton, ON, Canada., Khan H; School of Medicine, St. George's University, True Blue, Grenada., Chaudry E; Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada., Lahoud C; Department of Ophthalmology, General Hospital in Villeneuve-Saint-Georges, Villeneuve-Saint-Georges, France.
المصدر: Case reports in ophthalmology [Case Rep Ophthalmol] 2023 Aug 18; Vol. 14 (1), pp. 388-393. Date of Electronic Publication: 2023 Aug 18 (Print Publication: 2023).
نوع المنشور: Case Reports
اللغة: English
بيانات الدورية: Publisher: Karger AG Country of Publication: Switzerland NLM ID: 101532006 Publication Model: eCollection Cited Medium: Print ISSN: 1663-2699 (Print) Linking ISSN: 16632699 NLM ISO Abbreviation: Case Rep Ophthalmol Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Basel : Karger AG
مستخلص: Sickle cell disease (SCD), an inherited vaso-occlusive disorder, results in recurrent painful episodes and a variety of serious systemic complications that can lead to severe disabilities and even death. Here, we report a case of a 19-year-old African American patient with homozygous sickle cell trait who presented with right upper lid edema and ptosis, 3 days after his admission to the hospital following a sickle cell crisis. Initially, mistaken as a superinfection in the context of his disease, a diagnosis of orbital abscess was made. Intravenous antibiotics and a proper treatment plan were set accordingly. Only after extensive clinical and radiological examinations, it turned out to be an acute subperiosteal orbital hematoma, a rare clinical manifestation of SCD. The aim of our case report was to highlight the difference in orbital presentation between osteomyelitis and subperiosteal hematoma, as well as spreading awareness among medical professionals and especially ophthalmologists for this rare presentation of orbital wall infarction, as the initial differential diagnosis of SCD patients with ocular involvement.
Competing Interests: No conflict of interest in applicable (e.g., employment, consultancies, honoraria, stock ownership and options, expert testimony, grants or patents received or pending, royalties) which took place in the previous 3 years. The authors have no conflicts of interest to declare.
(© 2023 The Author(s). Published by S. Karger AG, Basel.)
التعليقات: Erratum in: Case Rep Ophthalmol. 2024 May 28;15(1):451. doi: 10.1159/000539444. (PMID: 38840899)
References: Lancet. 1997 Sep 6;350(9079):725-30. (PMID: 9291916)
Eye (Lond). 2001 Dec;15(Pt 6):774-80. (PMID: 11827001)
Am J Ophthalmol. 2008 Oct;146(4):595-601. (PMID: 18662809)
J Am Acad Orthop Surg Glob Res Rev. 2020 Sep;4(9):e20.00002-10. (PMID: 32890008)
BMC Ophthalmol. 2018 Aug 28;18(1):211. (PMID: 30153804)
Am J Ophthalmol Case Rep. 2020 Oct 28;20:100986. (PMID: 33163693)
Can J Ophthalmol. 2020 Apr;55(2):e55-e56. (PMID: 31712015)
Paediatr Respir Rev. 2014 Mar;15(1):4-12. (PMID: 24361300)
Int J Ophthalmol. 2020 Oct 18;13(10):1675-1677. (PMID: 33078122)
Ophthalmic Plast Reconstr Surg. 2019 Nov/Dec;35(6):e134-e136. (PMID: 31593047)
Acta Clin Belg. 2015 Dec;70(6):451-2. (PMID: 26790559)
Annu Rev Pathol. 2019 Jan 24;14:263-292. (PMID: 30332562)
J Craniofac Surg. 2020 Jan/Feb;31(1):e60-e61. (PMID: 31609957)
Lancet. 2010 Dec 11;376(9757):2018-31. (PMID: 21131035)
J Clin Imaging Sci. 2020 Dec 20;10:85. (PMID: 33408960)
فهرسة مساهمة: Keywords: Orbit; Osteomyelitis; Sickle cell disease; Sphenoid bone; Subperiosteal hematoma
تواريخ الأحداث: Date Created: 20231030 Latest Revision: 20240606
رمز التحديث: 20240606
مُعرف محوري في PubMed: PMC10601770
DOI: 10.1159/000532016
PMID: 37901617
قاعدة البيانات: MEDLINE
الوصف
تدمد:1663-2699
DOI:10.1159/000532016