Bilateral hypopyon in syphilitic uveitis

To report an atypical bilateral hypopyon presentation of syphilitic uveitis. A 38-year-old male presented with a 2-day history of bilateral progressive visual loss, conjunctival hyperemia, and photophobia. Initial ophthalmologic examination revealed bilateral hypopyon and vitritis that limited the e...

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Published inAmerican journal of ophthalmology case reports Vol. 21; p. 101007
Main Authors Gonzalez Collazo, Monica P., Rebollo Rodriguez, Nicole P., Santiago-Vazquez, Marely, Crespo-Ramos, Susanne M., Marcos-Martinez, Maria J., Villegas, Víctor M., Oliver, Armando L.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2021
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Abstract To report an atypical bilateral hypopyon presentation of syphilitic uveitis. A 38-year-old male presented with a 2-day history of bilateral progressive visual loss, conjunctival hyperemia, and photophobia. Initial ophthalmologic examination revealed bilateral hypopyon and vitritis that limited the examination of the posterior segment. The physical exam revealed cervical lymphadenopathy, glossal leukoplakia, erythematous maculae on the hard palate, erythematous macular lesions on both palms, onychodystrophy, onycholysis, and psoriasiform plaques on both plantar surfaces, testicular tenderness, and hypopigmented patches on the scrotal and perianal skin. A therapeutic and diagnostic vitrectomy was performed on the right eye, and the intraoperative findings were consistent with severe vitritis and pre-retinal precipitates. The cytopathologic analysis of the right vitreous revealed a mixed inflammatory process composed of lymphocytes, histiocytes, and neutrophils in a proteinaceous background. Laboratory testing revealed positive serum RPR, CSF FTA-Abs and VDRL, and HIV serology. Treatment with a 2-week course of intravenous penicillin G 4 million units every 4 hours and topical corticosteroids resulted in complete resolution of the uveitis. Bilateral hypopyon uveitis may be a rare presentation of syphilitic uveitis. As with most forms of uveitis, syphilis should be considered in the differential diagnosis of patients presenting with bilateral hypopyon.
AbstractList Purpose: To report an atypical bilateral hypopyon presentation of syphilitic uveitis. Observations: A 38-year-old male presented with a 2-day history of bilateral progressive visual loss, conjunctival hyperemia, and photophobia. Initial ophthalmologic examination revealed bilateral hypopyon and vitritis that limited the examination of the posterior segment. The physical exam revealed cervical lymphadenopathy, glossal leukoplakia, erythematous maculae on the hard palate, erythematous macular lesions on both palms, onychodystrophy, onycholysis, and psoriasiform plaques on both plantar surfaces, testicular tenderness, and hypopigmented patches on the scrotal and perianal skin. A therapeutic and diagnostic vitrectomy was performed on the right eye, and the intraoperative findings were consistent with severe vitritis and pre-retinal precipitates. The cytopathologic analysis of the right vitreous revealed a mixed inflammatory process composed of lymphocytes, histiocytes, and neutrophils in a proteinaceous background. Laboratory testing revealed positive serum RPR, CSF FTA-Abs and VDRL, and HIV serology. Treatment with a 2-week course of intravenous penicillin G 4 million units every 4 hours and topical corticosteroids resulted in complete resolution of the uveitis. Conclusions and Importance: Bilateral hypopyon uveitis may be a rare presentation of syphilitic uveitis. As with most forms of uveitis, syphilis should be considered in the differential diagnosis of patients presenting with bilateral hypopyon.
To report an atypical bilateral hypopyon presentation of syphilitic uveitis. A 38-year-old male presented with a 2-day history of bilateral progressive visual loss, conjunctival hyperemia, and photophobia. Initial ophthalmologic examination revealed bilateral hypopyon and vitritis that limited the examination of the posterior segment. The physical exam revealed cervical lymphadenopathy, glossal leukoplakia, erythematous maculae on the hard palate, erythematous macular lesions on both palms, onychodystrophy, onycholysis, and psoriasiform plaques on both plantar surfaces, testicular tenderness, and hypopigmented patches on the scrotal and perianal skin. A therapeutic and diagnostic vitrectomy was performed on the right eye, and the intraoperative findings were consistent with severe vitritis and pre-retinal precipitates. The cytopathologic analysis of the right vitreous revealed a mixed inflammatory process composed of lymphocytes, histiocytes, and neutrophils in a proteinaceous background. Laboratory testing revealed positive serum RPR, CSF FTA-Abs and VDRL, and HIV serology. Treatment with a 2-week course of intravenous penicillin G 4 million units every 4 hours and topical corticosteroids resulted in complete resolution of the uveitis. Bilateral hypopyon uveitis may be a rare presentation of syphilitic uveitis. As with most forms of uveitis, syphilis should be considered in the differential diagnosis of patients presenting with bilateral hypopyon.
ArticleNumber 101007
Author Gonzalez Collazo, Monica P.
Crespo-Ramos, Susanne M.
Santiago-Vazquez, Marely
Rebollo Rodriguez, Nicole P.
Marcos-Martinez, Maria J.
Villegas, Víctor M.
Oliver, Armando L.
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  surname: Oliver
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Keywords Infectious uveitis
Vitrectomy
Syphilis
Hypopyon
Uveitis
Language English
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2021 The Authors.
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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Snippet To report an atypical bilateral hypopyon presentation of syphilitic uveitis. A 38-year-old male presented with a 2-day history of bilateral progressive visual...
Purpose: To report an atypical bilateral hypopyon presentation of syphilitic uveitis. Observations: A 38-year-old male presented with a 2-day history of...
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StartPage 101007
SubjectTerms Case Report
Hypopyon
Infectious uveitis
Syphilis
Uveitis
Vitrectomy
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Title Bilateral hypopyon in syphilitic uveitis
URI https://dx.doi.org/10.1016/j.ajoc.2020.101007
https://www.ncbi.nlm.nih.gov/pubmed/33437894
https://pubmed.ncbi.nlm.nih.gov/PMC7788489
https://doaj.org/article/df7c26cea1da49e8a4b7d907495f6d8c
Volume 21
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