1.Poliosis of Eyelashes as an Unusual Sign of a Halo Nevus.
Kyu Mee KAY ; Joong Hun KIM ; Tae Soo LEE
Korean Journal of Ophthalmology 2010;24(4):237-239
A 39-year-old man with poliosis of his lower eyelid lashes visited our clinic. He reported that his symptoms began with a few central lashes and then spread along the adjacent lashes during the ensuing 2 weeks. A pigmented nevus, approximately 4 mm in diameter, was identified just above the white lashes without surrounding skin depigmentation. No specific findings were identified with regard to the patient's general health or serologic and radiologic testing. Excisional biopsy of the pigmented nevus was performed. On histopathologic examination, infiltration of the dermis by numerous lymphocytes and melanophages was observed. The poliosis was ultimately diagnosed as a presenting sign of the halo phenomenon in the regressive stage of a melanocytic nevus.
Adult
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Biopsy
;
Diagnosis, Differential
;
Eyelashes/*pathology
;
Eyelid Neoplasms/*diagnosis
;
Hair Diseases/*diagnosis
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Humans
;
Hypopigmentation
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Male
;
Nevus, Halo/*diagnosis
2.The Effect of Epiblepharon Surgery on Visual Acuity and With-the-Rule Astigmatism in Children.
Na Mi KIM ; Jae Ho JUNG ; Hee Young CHOI
Korean Journal of Ophthalmology 2010;24(6):325-330
PURPOSE: To evaluate the effect of epiblepharon surgery on visual acuity and with-the-rule astigmatism in children compared to patients without surgical treatment. METHODS: We undertook a retrospective case control study and reviewed the charts of 202 eyes treated with epiblepharon surgery and of 142 eyes without surgery. The surgical procedure for epiblepharon correction used rotating suture techniques. Data regarding age, best corrected visual acuity, and degree of astigmatism were recorded. Baseline and 1-, 3-, 6-, and 12-month postoperative data were collected. The chi-square test, Student's t-test and general linear model analysis for repeated measures were applied. RESULTS: The mean astigmatism in the surgical group decreased from 1.10 +/- 1.02 diopter (D) preoperatively to 0.84 +/- 1.05 D at 3 months after surgery (p < 0.05). However, there was no statistically significant difference compared to the non-surgical group during the first year. The general linear model analysis comparing the mean astigmatism between the two groups over time showed a significant group-time interaction (p < 0.05). Within the surgical group, the higher baseline astigmatic subgroup and the 5- to 8-year-old group demonstrated greater cylinder reduction over time. The change in mean visual acuity was not significant in either group. CONCLUSIONS: Significant astigmatic reduction was found after surgical correction in epiblepharon patients. Patients with higher baseline astigmatism exhibited greater astigmatic reduction after epiblepharon surgery. These results suggest that, in order to reduce astigmatism, an epiblepharon operation should be considered in patients with a high level of astigmatism.
Astigmatism/*etiology/*physiopathology
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Case-Control Studies
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Child
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Child, Preschool
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Eye Abnormalities/*complications/*surgery
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Eyelashes/pathology
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Eyelids/*abnormalities/pathology/surgery
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Female
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Humans
;
Male
;
Retrospective Studies
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Treatment Outcome
;
*Visual Acuity
3.Genetic analysis and clinical phenotype of a family with lymphedema-distichiasis syndrome.
Gang HU ; Bei LIU ; Min CHEN ; Yeqing QIAN ; Minyue DONG
Journal of Zhejiang University. Medical sciences 2020;49(5):581-585
OBJECTIVE:
To identify the genetic causes of a family with lymphedema-distichiasis syndrome (LDS).
METHODS:
The whole exome sequencing was performed in a aborted fetus as the proband, and a candidate gene was identified. Peripheral blood of 8 family members were collected. Genotypic-phenotypic analysis were carried out through PCR amplification and Sanger sequencing.
RESULTS:
The proband, and the mother, grandmother, uncle, granduncle of the proband all had distichiasis or varix of lower limb carried a
CONCLUSIONS
The
Aborted Fetus/physiopathology*
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Adult
;
Eyelashes/pathology*
;
Female
;
Forkhead Transcription Factors/genetics*
;
Frameshift Mutation
;
Humans
;
Lymphedema/pathology*
;
Male
;
Phenotype
;
Pregnancy
;
Whole Exome Sequencing