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Search Results: 1 - 10 of 20966 matches for " Kim Usha "
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Arora Vipul,Usha Kim,Khazei Hadi
Indian Journal of Ophthalmology , 2010,
Abstract:
Congenital unilateral ocular fibrosis syndrome secondary to benign congenital tumor
Vijayalakshmi P,Jethani Jitendra,Kim Usha
Indian Journal of Ophthalmology , 2006,
Abstract: Congenital unilateral fibrosis, blepharoptosis and enophthalmos syndrome is one of the rare forms of congenital fibrosis of extraocular muscles. The nature and cause of such unilateral inflammation leading to fibrosis is unknown. Prenatal orbital penetration has been proposed as a cause of this syndrome. We report a case of this rare syndrome associated with an adjacent sinus tumor.
Delleman Oorthuys syndrome: ′Oculocerebrocutaneous syndrome′
Arora Vipul,Kim Usha,Khazei Hadi
Indian Journal of Ophthalmology , 2009,
Abstract: Delleman Oorthuys syndrome (oculocerebrocutaneous syndrome) is a rare, congenital sporadic disorder affecting the skin and central nervous system. We present the case of a one-month-old male who presented with an orbital cyst in the left eye since birth along with other manifestations of this syndrome. The manifestations of this syndrome resemble other developmental disorders like Goldenhar and Goltz syndrome. Conservative management of the orbital cyst in these cases have been described. The need to diagnose this rare congenital anomaly with cerebral malformations as a separate entity is crucial in the management of these children.
Ophthalmic complications including retinal detachment in hyperimmunoglobulinemia E (Job′s) syndrome: Case report and review of literature
Arora Vipul,Kim Usha,Khazei Hadi,Kusagur Shivayogi
Indian Journal of Ophthalmology , 2009,
Abstract: Hyperimmunoglobulinemia E (Job′s) syndrome is characterized by markedly increased levels of immunoglobulin E, recurrent cutaneous and systemic pyogenic infections, atopic dermatitis, and peripheral eosinophilia. Although ocular involvement in Job′s syndrome is rare, there are reports of keratoconus, staphylococcal chalazia with blepharitis, and endophthalmitis by various authors. We present the first case report of retinal detachment with complicated cataract in Job′s syndrome.
Clinical features and management of posttraumatic subperiosteal hematoma of the orbit
Kim Usha,Arora Vipul,Shah Akash,Solanki Urvashi
Indian Journal of Ophthalmology , 2011,
Abstract: Traumatic subperiosteal hematoma (SpH) usually presents late, after the initial trauma. It is generally seen in young males. Computed tomography is the best mode of imaging and helps to rule out orbital fracture or associated subdural hematoma. We present the clinical features and management of four patients seen at the orbit clinic with SpH. Management is based on time of presentation, visual acuity and any communicating bleed. The prognosis of traumatic SpH is excellent if treated with an individualized patient approach.
Atypical presentation of an unusual foreign body
Arora Vipul,Kim Usha,Shetty Shashikant,Shah Akash
Indian Journal of Ophthalmology , 2010,
Abstract: A 14-year-old boy presented with intractable diplopia for 10 days following an assault. A thorough history revealed that he was unaware of any penetrating injury. However, imaging demonstrated a radiolucent foreign body between the globe and the orbital floor. On surgical exploration, it was found to be the proximal part of a ball point pen. Its removal resulted in complete resolution of diplopia. Thorough clinical and radiological examination is recommended when a foreign body is suspected in pediatric patients. Prompt diagnosis will aid in early intervention and prevention of long-term complications.
Authors′ reply
Arora Vipul,Usha Kim,Khazei Hadi,Kusagur Shivayogi
Indian Journal of Ophthalmology , 2010,
Abstract:
Case report: Ocular malformation with a ′double globe′ appearance
Kim Usha,Arora Vipul,Shah Akash,Srinivasan K
Indian Journal of Radiology and Imaging , 2009,
Abstract: Colobomatous cyst of the orbit is a rare congenital cystic malformation associated with ocular maldevelopment. Usually, the cyst is associated with a microphthalmic globe. We present a rare case of a unilateral large colobomatous cyst associated with a normal-sized globe, giving the appearance of a double globe on imaging.
Multimodality treatment approach in management of primary peripheral primitive neuroectodermal tumor of the orbit
Kim Usha,Arora Vipul,Devanand J,Khazei Hadi
Indian Journal of Ophthalmology , 2009,
Abstract: Primitive neuroectodermal tumor is a small round cell malignancy which rarely involves the orbit. We report a case of a two-year old male child presenting as unilateral eccentric proptosis with extraconal and intraconal mass, diagnosed as primary peripheral primitive neuroectodermal tumor (pPPNET) on histopathology and immunohistochemistry. There is no defined consensus in the management of these tumors due to its rare presentation. We describe its distinguishing features with emphasis on multimodal and aggressive treatment approach which ensures appropriate management of these cases.
RPE Adenocarcinoma as the Presenting Sign of Bronchogenic Carcinoma: Diagnostic Dilemma in the Management of a Case
Namrata Adulkar,Santhi Radhakrishnan,N. Vidhya,Usha Kim
Case Reports in Ophthalmological Medicine , 2013, DOI: 10.1155/2013/786378
Abstract:
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