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1.
J Fr Ophtalmol ; 32(2): 98-103, 2009 Feb.
Article in French | MEDLINE | ID: mdl-19515322

ABSTRACT

INTRODUCTION: Vitreous hemorrhage is a frequent complication of proliferated diabetic retinopathy. Vitrectomy has vastly improved its prognosis. The purpose of this study was to evaluate the use of silicone oil in vitreal surgery in this indication. METHODS: We present a retrospective study of 15 eyes that underwent vitrectomy and silicone oil injection for vitreal hemorrhage complicating proliferative diabetic retinopathy. For each patient, we noted the clinical and echographic features, the surgical procedure, and the postoperative outcome after a mean period of 20 months. RESULTS: The indications for silicone injection were recurrent vitreal hemorrhage (seven eyes), aggressive fibrovascular proliferations (five eyes), and iatrogenic retinal breaks (three eyes). Anatomic success was noted in ten cases. Four patients had a hemorrhage reoccurrence after silicone oil removal and one patient developed neovascular glaucoma. Silicone cataract (seven eyes) and emulsification of silicone (one eye) were noted. DISCUSSION: The use of silicone oil in vitreal surgery for complicated proliferated diabetic retinopathy contributes a hemostatic and plugging effect, but it still has a number of disadvantages such as the need to remove it and its own side effects. It can be beneficial in cases of rubeosis or recurrent hemorrhage. However, it is essentially indicated in recurrent hemorrhage in monophthalmos patients.


Subject(s)
Diabetic Retinopathy/complications , Hemostatic Techniques , Silicone Oils/administration & dosage , Vitreous Hemorrhage/etiology , Vitreous Hemorrhage/therapy , Adult , Female , Humans , Male , Middle Aged , Retrospective Studies
2.
Bull Soc Belge Ophtalmol ; (303): 51-4, 2007.
Article in French | MEDLINE | ID: mdl-17894288

ABSTRACT

INTRODUCTION: Peters anomaly is a primitive congenital glaucoma characterised by a central corneal leukoma. Therefore, keratoplasty is essential in addition to the specific treatment of the glaucoma. We aim to study the particularities and the evolutional ways of penetrating keratoplasty in Peters anomaly by presenting a clinical case treated in our service. CLINICAL CASE: Female baby aged 1 month, addressed for bilateral corneal leukoma. On examination he presented no ocular pursuit, a nystagmus and a megalocornea. Clinical features concluded to congenital glaucoma associated to Peters anomaly. The patient underwent trabeculectomy with Mitomycine C application. At the age of 2 1/2 years, and with an equilibrated eye pressure, she underwent penetrating keratoplasty using a 8,5mm diameter corneal graft. After 2 months the nystagmus decreased, and the vision improved, permitting an easier walk for the child. CONCLUSION: Peters anomaly is a frequent cause of congenital glaucoma, where penetrating keratoplasty is essential for corneal transparency. It necessitates a good eye pressure control.


Subject(s)
Cornea/abnormalities , Cornea/surgery , Corneal Opacity/surgery , Corneal Transplantation/methods , Glaucoma/congenital , Glaucoma/surgery , Corneal Opacity/etiology , Female , Glaucoma/etiology , Humans , Infant, Newborn
4.
J Fr Ophtalmol ; 29(4): 413-7, 2006 Apr.
Article in French | MEDLINE | ID: mdl-16885809

ABSTRACT

INTRODUCTION: Iris mammillations are congenital abnormalities characterized by vitiliform protuberances regularly spaced on the surface of a velvety iris. They can be either isolated or associated with melanocytosis involving iris, sclera or periocular tissues, resulting in a risk for uveal melanoma. They can be complicated by ocular hypertension. We report three cases of iris mammillations in three children. CASES REPORT: For each patient, age, circumstances of revelation, anterior and posterior segment examination, intraocular pressure, associated anomalies, and progression were noted. Patient no. 1: In a 13-month-old boy examined for a squint, bilateral iris mammillations were fortuitously discovered. Intraocular pressure remained normal over 22 months of follow-up. Patient no. 2: In an eight-year-old boy, bilateral iris mammillations with papillary excavation were fortuitously discovered. Intraocular pressure was normal and the excavation did not change over 20 months of follow-up. Patient no. 3: A five-year-old boy was examined for a scleral pigmentation in the right eye. The examination found unilateral iris mammillations and ipsilateral ocular melanocytosis. Intraocular pressure and fundus were normal and remained normal over 13 months of follow-up. DISCUSSION: and conclusion: Iris mammillations are congenital abnormalities, generally unilateral, sometimes hereditary. The differential diagnosis includes Lisch nodules of neurofibromatosis and iris melanoma. The etiology of iris mammillations is unknown; these lesions can be complicated by ocular hypertony and, in case of associated melanocytosis of the iris, sclera or periocular tissues, by uveal melanoma. These potential complications warrant a regular clinical follow-up.


Subject(s)
Iris Diseases/pathology , Child , Child, Preschool , Humans , Infant , Male , Melanosis/pathology , Retrospective Studies
5.
J Fr Ophtalmol ; 29(3): 302-6, 2006 Mar.
Article in French | MEDLINE | ID: mdl-16557175

ABSTRACT

AIM: To report two cases of Vogt-Koyanagi-Harada syndrome (VKH) complicated by subretinal neovascularization. CASE REPORTS: The first patient was a 12-year-old girl in whom choroidal neovascularization occurred after VKH had evolved for 9 months. Fundus examination of the left eye revealed a macular extrafoveolar superior serous retinal detachment (SRD) centered by a grey-white pseudo-tumoral zone. A crown of exudates lined the SRD. Pigment epithelium impairment was substantial. Fluorescein angiography showed an early intensive and diffuse staining in the left eye corresponding to a neovascular membrane associated with a late impregnation of the SRD. Green monochromatic laser photocoagulation was considered but refused by the parents. The second patient was an 18-year-old girl followed up for VKH for 2 years. Ophthalmoscopy showed a serous retinal detachment with hemorrhage and hard exudates in the right eye. Fluorescein angiography showed early staining in the juxtapapillary region corresponding to a juxtapapillary neovascular membrane. High-dose systemic corticotherapy was instituted. Photocoagulation was not indicated because of the juxtapapillary topography of the neovascular membrane. CONCLUSION: VKH is a bilateral panuveitis that can be complicated by subretinal neovascularization in 2.5%-10% of cases. This complication must be diagnosed early. We discuss angiogenic factors and therapeutic modalities.


Subject(s)
Retinal Neovascularization/etiology , Uveomeningoencephalitic Syndrome/complications , Adolescent , Child , Female , Humans
6.
J Fr Ophtalmol ; 28(7): 765-8, 2005 Sep.
Article in French | MEDLINE | ID: mdl-16208228

ABSTRACT

INTRODUCTION: Phtiriasis palperarum is an unusual cause of blepharitis. This ectoparasitic infestation of the lashes is more frequent in adult; a pubic attack is usually associated. It is however rare in children. The goal of our study is to bring back four observations of infantile phtiriasis palpebrarum. PATIENTS AND METHODS: Four children presented themselves for palpebral itching and ocular redness. Slit lamp examination revealed evidence of small parasites attached to the proximal extreme of the eyelashes. A survey within the family was carried out and parasitological examination was realized. RESULTS: Parasitological examination had identified adult forms and nits of phtirus pubis. The bed linen was the way of contamination. Mechanical extraction of the parasite was tried but was very painful. Two patients were treated with a regimen of 1% yellow oxide of mercury ointment four times daily for 14 days, the two others was treated by Vaseline pomade because of a very important palpebral irritation. Evolution was favorable among all patients. DISCUSSION: We discuss in this work the ways of contamination of phtiriasis palpebrarum in children. In fact, eyelashes contamination in children is secondary to a contact with an adult carrier of a pubic phtiriasis. The transmission can be done following sexual maltreatments or by the means of infected clothing or bed linen. The diagnosis of phtiriasis palpebrarum is clinical confirmed by parasitological examination. Different therapeutic were proposed, the mechanical treatment must be carried out but it is seldom sufficient and it is often necessary to associate a chemical treatment (malathion to 1%, mercury oxide with 1%, fluorescein with 20%...) or physical treatment (cryotherapy, laser argon). CONCLUSION: Diagnosis of phtiriasis palpebrarum is easy and requires the detection of the source of contamination in order to prevent reinfestations.


Subject(s)
Blepharitis/parasitology , Eyelashes , Lice Infestations/diagnosis , Lice Infestations/drug therapy , Phthirus , Animals , Child , Child, Preschool , Female , Humans , Male
7.
J Fr Ophtalmol ; 27(10): 1146-9, 2004 Dec.
Article in French | MEDLINE | ID: mdl-15687925

ABSTRACT

INTRODUCTION: Seborrheic keratosis is the most frequent palpebral tumor, observed for the most part in the second half of life. It may be confused clinically with a basal cell carcinoma or a melanoma. The histopathological study confirms the diagnosis. OBSERVATION: A 69-year-old man presented with a giant superior palpebral tumor leading to ptosis of the eyelid, which had evolved over 5 years. Examination found a pigmented cerebriform multilobed granulated mass, with a smooth surface and a more or less seborrheic aspect, pedicled in places, covering the entire eyelid but sparing the internal angle. This aspect suggested melanoma, basal cell carcinoma or seborrheic keratosis. Histological biopsy revealed basal cell carcinoma. Excision with palpebral reconstitution using palpebral flaps was performed. The histopathological analysis of the tumor concluded in seborrheic keratosis. DISCUSSION: Seborrheic keratosis is a frequent tumor of the face and eyelids. Its highly pigmented clinical aspect can be confounded with a nevus or a melanoma, whereas the histological aspect can suggest basal cell carcinoma or squamous cell carcinoma, but the basal membrane is always intact. Several treatments have been proposed, including electrocoagulation, cryotherapy, dermabrasion, as well as CO2 laser treatment. However, when there is doubt with regard to the histological nature, surgery is preferred. CONCLUSION: This was a case of seborrheic keratosis, atypical in that it covered the entire upper eyelid and produced a highly disfiguring aspect and functional problems, requiring surgical treatment with eyelid reconstruction.


Subject(s)
Eyelid Diseases , Keratosis, Seborrheic , Aged , Eyelid Diseases/pathology , Eyelid Diseases/surgery , Humans , Keratosis, Seborrheic/pathology , Keratosis, Seborrheic/surgery , Male
8.
Tunis Med ; 79(3): 157-60, 2001 Mar.
Article in French | MEDLINE | ID: mdl-11471444

ABSTRACT

UNLABELLED: To demonstrate advantages of using subconjunctival injections of clindamycin in the treatment of toxoplasmic retinchoroiditis. METHODS: A prospective study was conducted in 13 patients with unilateral toxoplasmic retinochoroiditis. All cases were treated with subconjunctival injections of clindamycin in association with general corticosteroïds. Mean follow-up was 7.6 months. RESULTS: Subjective improvement of the visual acuity was obtained in 67% during the first week. Cicatrization was obtained in 1.4 months on average. Recurrences were developed in 15% of cases. Clindamycin did not produce any general side effects, however a conjunctival inflammation and keratitis were observed in one case caused by an error in concentration of clindamycin. Subconjunctival injections of clindamycin provide an interesting alternative in the choice of antitoxoplasmic ocular therapy.


Subject(s)
Chorioretinitis/drug therapy , Chorioretinitis/etiology , Clindamycin/administration & dosage , Clindamycin/pharmacology , Toxoplasmosis, Ocular/complications , Toxoplasmosis, Ocular/drug therapy , Adolescent , Adult , Cicatrix , Conjunctiva , Female , Humans , Inflammation , Keratitis/etiology , Male , Middle Aged , Prospective Studies , Recurrence , Treatment Outcome
9.
J Fr Ophtalmol ; 24(8): 823-8, 2001 Oct.
Article in French | MEDLINE | ID: mdl-11894532

ABSTRACT

PURPOSE: The surgical management of pterygium is often complicated by recurrence of disease. The goal of this study was to compare three different surgical techniques used for the treatment of pterygium. METHOD: We propose a prospective and partly retrospective study on 167 cases of pterygium 151 were primary and 16 were recurrent, treated between 1 January, 1995 and 30 June, 1998. The surgical treatment used of 3 different techniques: pterygium excision for 111 eyes, pterygium excision with conjunctival autograft for 29 eyes, pterygium excision with application of mitomycin C for 27 eyes. RESULTS: Immediate results for the three kinds of treatment were good. No serious complications were noted. Long-term results show a recurrence rate of 10.3% for conjunctival autograft, 11.1% for mitomycin C application, while the pterygium excision alone had a recurrence rate of 55.9%. CONCLUSION: This study demonstrated that conjunctival autografting and the application of mitomycin C are safe surgical techniques that reduce the probability of recurrence after surgery for pterygium. They can be recommended for young people and patients exposed to sun. Mitomycin therapy is the most appropriate treatment for these cases, because of its simplicity, lower lost and the relative lack of complication.


Subject(s)
Pterygium/surgery , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Ophthalmologic Surgical Procedures/methods , Prospective Studies , Retrospective Studies
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