Clinical features of 10 cases of eyelid sporotrichosis in Jilin Province (Northeast China)
Abstract Objective Sporotrichosis is a common subcutaneous mycosis caused by an infection with dimorphic fungus Sporothrix schenckii . We present a series of patients with eyelid sporotrichosis and study the clinical and histopathological presentation, microbiology, treatment options, and outcome. M...
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Published in | Canadian journal of ophthalmology Vol. 51; no. 4; pp. 297 - 301 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Inc
01.08.2016
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Subjects | |
Online Access | Get full text |
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Summary: | Abstract Objective Sporotrichosis is a common subcutaneous mycosis caused by an infection with dimorphic fungus Sporothrix schenckii . We present a series of patients with eyelid sporotrichosis and study the clinical and histopathological presentation, microbiology, treatment options, and outcome. Methods A retrospective case-series study of patients with a clinical diagnosis of eyelid sporotrichosis. Records were examined to obtain information regarding patient demographics, presenting symptoms and signs, histopathological examination, microbiology, management, and outcomes. Results Ten patients (4 men, 6 women; mean age 46.5 years, range 3–81 years) were included. Based on their clinical manifestations, eyelid sporotrichosis was classified into 3 major forms: ( i ) fixed cutaneous (6/10 cases), ( ii ) lymphocutaneous (3/10 cases), and ( iii ) eyelid abscess (1/10 cases). All the cases were treated with a terbinafine 12-week regimen. Nodules, papules, and abscesses regressed after treatment. No recurrence was discovered after a 12-week follow-up. Conclusions Eyelid sporotrichosis has typical features of clinical manifestations. Histopathological examination and tissue culture are helpful for diagnosis. Confirmed cases normally require long-term systematic treatment with antifungal agents, but surgical removal is normally unnecessary. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0008-4182 1715-3360 |
DOI: | 10.1016/j.jcjo.2016.02.018 |