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A Case of Primary Neurofibroma of Lacrimal Sac
Article in Korean | WPRIM (Western Pacific) | ID: wpr-101548
Responsible library: WPRO
ABSTRACT
Lacrimal sac tumors are relatively rare and epithelial origin, mostly. The clinical menifestations of lacrimal sac tumors include epiphora, chronic dacrtocystitis, or lacrimal mass. Primary neurofibroma of lacrimal sac is benign nature and malignant transformation is rare. But malignant lacrimal sac tumors can be life-threatening; Therefore, the early diagnosis and treatment are important. We reported an experience of a 37-year-old female who had epiphora, pruritis, lacrimal mass, and facial asymmetry. The patient was finally diagnosed with pigmented neurofibroma of lacrimal sac that was proven by dacryocystogram, CT scan, and histophthologic finding.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Pruritus / Tomography, X-Ray Computed / Early Diagnosis / Facial Asymmetry / Lacrimal Apparatus Diseases / Neurofibroma Type of study: Diagnostic study / Screening study Limits: Adult / Female / Humans Language: Korean Journal: Journal of the Korean Ophthalmological Society Year: 1998 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Pruritus / Tomography, X-Ray Computed / Early Diagnosis / Facial Asymmetry / Lacrimal Apparatus Diseases / Neurofibroma Type of study: Diagnostic study / Screening study Limits: Adult / Female / Humans Language: Korean Journal: Journal of the Korean Ophthalmological Society Year: 1998 Document type: Article
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