1.Surgical Correction of Hallermann-Streiff Syndrome: A Case Report of Esotropia, Entropion, and Blepharoptosis.
Won Kyung CHO ; Joo Wan PARK ; Mi Ra PARK
Korean Journal of Ophthalmology 2011;25(2):142-145
We report a case of surgical treatment for Hallermann-Streiff syndrome in a patient with ocular manifestations of esotropia, entropion, and blepharoptosis. A 54-year-old man visited Yeouido St. Mary's Hospital complaining of ocular discomfort due to cilia touching the corneas of both eyes for several years. He had a bird-like face, pinched nose, hypotrichosis of the scalp, mandibular hypoplasia with forward displacement of the temporomandibular joints, a small mouth, and proportional short stature. His ophthalmic features included sparse eyelashes and eyebrows, microphthalmia, nystagmus, lower lid entropion in the right eye, and upper lid entropion with blepharoptosis in both eyes. There was esodeviation of the eyeball of more than 100 prism diopters at near and distance, and there were limitations in ocular movement on lateral gaze. The capsulopalpebral fascia was repaired to treat the right lower lid entropion, but an additional Quickert suture was required to prevent recurrence. Blepharoplasty and levator palpebrae repair were performed for blepharoptosis and dermatochalasis. Three months after lid surgery, the right medial rectus muscle was recessed 7.5 mm, the left medial rectus was recessed 7.25 mm, and the left lateral rectus muscle was resected 8.0 mm.
Blepharoptosis/physiopathology/*surgery
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Entropion/physiopathology/*surgery
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Esotropia/physiopathology/*surgery
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Eye Movements
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Follow-Up Studies
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Hallermann's Syndrome/*surgery
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Humans
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Male
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Middle Aged
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Oculomotor Muscles/physiopathology/*surgery
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Ophthalmologic Surgical Procedures/*methods
2.Consecutive Esodeviation After Exotropia Surgery in Patients Older than 15 Years: Comparison with Younger Patients.
Hye Jin PARK ; Sang Mook KONG ; Seung Hee BAEK
Korean Journal of Ophthalmology 2008;22(3):178-182
PURPOSE: The purpose of this study was to investigate the clinical course of esodeviation after exotropia surgery in older patients (older than 15 years) and to compare it with that in younger patients (15 years or younger). METHODS: The medical records of all surgeries for exodeviation from December 2004 to February 2007 were reviewed and 82 patients were found with consecutive esodeviation. The patients were divided into two groups according to their age: Group A (patients older than 15 years) and Group B (patients age 15 or younger). The clinical course of esodeviation in Group A was compared to that in Group B by means of survival analysis. RESULTS: The median survival times of the esodeviation were 2.0+/-0.1 months in Group A and 1.0+/-0.1 months in Group B (p=0.40). The prevalence of consecutive esotropia at six months was 0% in Group A and 6.1% in Group B (p=0.32). The myopic refractive error, worse sensory condition, and a larger preoperative exodeviation in Group A did not affect the clinical course of the two groups differently. CONCLUSIONS: The postoperative esodeviation of patients older than 15 years after exotropia surgery tended to persist longer during the early postoperative period than that of patients 15 years or younger, however, the difference did not persist at postoperative six months.
Adult
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Age Factors
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Child
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Esotropia/*etiology/physiopathology
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Exotropia/*surgery
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Female
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Humans
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Kaplan-Meiers Estimate
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Male
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Oculomotor Muscles/*surgery
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*Postoperative Complications
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Vision, Binocular/physiology
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Visual Acuity/physiology
3.Antielevation Syndrome after Unilateral Anteriorization of the Inferior Oblique Muscle.
Yoonae A CHO ; Jun Heon KIM ; Seunghyun KIM
Korean Journal of Ophthalmology 2006;20(2):118-123
PURPOSE: To report antielevation syndrome with restriction of elevation on abduction in the operated eye and overaction (OA) of the inferior oblique muscle (IO) of the contralateral eye after unilateral IO anteriorization (AT). METHODS: Medical records were reviewed retrospectively in 8 of 24 patients who underwent unilateral IOAT. Four patients were referred from other hospitals after the same surgery. RESULTS: Four patients had infantile esotropes. The rest showed accommodative esotropia, superior oblique palsy, exotropia, and consecutive exotropia. The mean amount of hyperdeviation was 16.3 PD (10~30). The mean restriction of elevation on abduction in the operated eye was -1.6 (-1~-4) and IOOA of the contralateral eye was +2.7 (+2~+3). IOAT of nonoperated eyes in 4 patients, IO weakening procedure of anteriorized eyes in 2 patients, and IO myectomy on an eye with IOAT in 1 patient were performed. Ocular motility was improved after surgery in all patients. CONCLUSIONS: Unilateral IOAT may result in antielevation syndrome. Therefore bilateral IOAT is recommended to balance antielevation in both eyes. A meticulous caution is needed when performing unilateral IOAT.
Syndrome
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Retrospective Studies
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Reoperation
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Postoperative Complications
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*Ophthalmologic Surgical Procedures
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Oculomotor Muscles/physiopathology/*surgery
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Ocular Motility Disorders/*etiology/physiopathology/surgery
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Infant
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Humans
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Follow-Up Studies
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Female
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Eye Movements/*physiology
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Exotropia/surgery
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Esotropia/surgery
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Child, Preschool
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Child
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Adult
4.The Clinical Course of Consecutive Esotropia after Surgical Correction.
Korean Journal of Ophthalmology 2007;21(4):228-231
PURPOSE: To investigate the clinical course in patients who underwent surgical correction of consecutive esotropia. METHODS: The medical records of 13 patients who underwent surgical correction of consecutive esotropia were reviewed retrospectively. The authors investigated the deviation and surgical method at the time of exotropia surgery. During the follow up period, the authors also studied incidence of amblyopia development, the effect of occlusion therapy, surgical methods for consecutive esotropia, and postoperative change of deviation. RESULTS: The average exodeviation was 27.1 prism diopter (PD). Bilateral lateral rectus muscle recession was performed in all patients. In all patients, alternate occlusion was tried from 2 weeks after development of consecutive esotropia. However, there was no effect on 7 patients. None of the patients developed amblyopia. Surgery for consecutive esotropia was performed on the average 15.3 months after exotropia surgery. The average esodeviation was 21.1PD. Medial rectus muscle recession was performed in 10 patients and lateral rectus muscle advancement in 3 patients. The average deviation of the subject group immediately after surgery was 1.2PD esodeviation, 0.9PD esodeviation one month after surgery, 2.4PD exodeviation 6 months after surgery, and 4.7PD exodeviation at the last follow up, and it showed a tendency to progress to exodeviation as the follow up period increased. Ten patients (76.9%) showed deviation within 8PD at the last follow up. CONCLUSIONS: The success rate of surgical correction for consecutive esotropia was a favorable outcome. But, careful decisions of the surgical method and amount is needed because the conversion of exodeviation during long-term follow-up is possible.
Adolescent
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Child
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Child, Preschool
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Esotropia/epidemiology/*etiology/physiopathology
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Exotropia/physiopathology/*surgery
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Eye Movements/*physiology
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Female
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Follow-Up Studies
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Humans
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Incidence
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Male
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Oculomotor Muscles/physiopathology/*surgery
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Ophthalmologic Surgical Procedures/*methods
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Postoperative Complications
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Retrospective Studies
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Time Factors
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Treatment Outcome
5.Consecutive Esotropia in Intermittent Exotropia Patients with Immediate Postoperative Overcorrection More Than 17 Prism Diopters.
Hyoung Seok KIM ; Young Woo SUH ; Seung Hyun KIM ; Yoonae A CHO
Korean Journal of Ophthalmology 2007;21(3):155-158
PURPOSE: To report the incidence and the factors of consecutive esotropia (ET) in patients with immediate postoperative overcorrection of at least 17 prism diopters (PD) after surgery for intermittent exotropia (X(T)). METHODS: Four-hundred-five patients under the age of 18 were included in this study. They underwent bilateral lateral rectus recession (LROU-rec) or unilateral recession-resection (R&R) for X(T). On postoperative day one, the patients with at least 17 PD overcorrection were classified as group 1 and those with less than 17 PD as group 2. Age, refractive error, type of surgery, lateral incomitancy, and the incidence of consecutive ET were analyzed for each group. RESULTS: Group 1 consisted of 116 patients (28.6%) and group 2 consisted of 289 (71.4%). At the six-month follow-up visit, consecutive ET had developed in 16 patients (13.8%) in group 1, and in five patients (1.7%) in group 2 (p<0.001). The occurrence of consecutive ET was not related to age at the time of surgery (p=0.46 in group 1 ; p=0.54 in group 2), refractive error (p=0.18 in group 1 ; p=0.08 in group 2), or the type of surgery (p=0.69 in group 1 ; p=1.00 in group 2). The incidence in group 1 was 23.8% in patients with lateral incomitancy and 8.1% in patients without lateral incomitancy (p<0.05). In group 2, the incidence was 4.4% in patients with lateral incomitancy and 0.5% in patients without lateral incomitancy (p=0.04). CONCLUSIONS: Consecutive ET developed in 13.8% of patients with immediate overcorrection of at least 17 PD. Lateral incomitancy was the most important risk factor.
Adolescent
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Child
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Child, Preschool
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Esotropia/*epidemiology/etiology/*physiopathology
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Exotropia/physiopathology/*surgery
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Female
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Follow-Up Studies
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Humans
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Incidence
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Male
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Oculomotor Muscles/surgery
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Ophthalmologic Surgical Procedures/*adverse effects
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Severity of Illness Index
6.Acute Comitant Esotropia in a Child With a Cerebellar Tumor.
Jong Min LEE ; Sin Hoo KIM ; Jeong Il LEE ; Ji Yong RYOU ; Sook Young KIM
Korean Journal of Ophthalmology 2009;23(3):228-231
We report a case of acute comitant esotropia in a child with a cerebellar tumor. A 3-year-old boy was referred for management of a 9 month history of acute acquired comitant esotropia. On first presentation, the patient's angle of esodeviation was 50 prism-diopters (PD) at distance and near fixation without any lateral incomitance. The cycloplegic refraction revealed +0.75 diopters in both eyes. Very mild bilateral papilledema was found on the fundus examination, but the neurological examination did not reveal any other pathological findings. Brain MRI showed a 5 cm mass located in the midline of the cerebellum as well as hydrocephalus. The mass was completely excised and histological examination confirmed the diagnosis of pilocytic astrocytoma. Despite neurosurgery, the patient's strabismus remained unresolved. One year after neurosurgery, both medial rectus muscles were surgically recessed by 6 mm, resulting in esotropia of 8PD at distant and near fixation without restoration of bifoveal fusion at follow-up 2 years after the eye muscle surgery. Therefore, acute onset comitant esotropia in a child can be the first sign of a cerebellar tumor, even without any other neurological signs and symptoms.
Acute Disease
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Astrocytoma/*complications/surgery
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Brain/pathology
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Cerebellar Neoplasms/*complications/diagnosis/surgery
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Child, Preschool
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Esotropia/*etiology/pathology/physiopathology/surgery
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Humans
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Magnetic Resonance Imaging
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Male
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Neurosurgical Procedures
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Oculomotor Muscles/surgery
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Refraction, Ocular
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Time Factors