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All Journal Medicina E-Jurnal Medika Udayana Jurnal Administrasi Bisnis Jurnal Kesehatan Prima ISM (Intisari Sains Medis) : Jurnal Kedokteran Ophthalmologica Indonesiana
Ni Made Laksmi Utari
Bagian Ilmu Kesehatan Mata Fakultas Kedokteran, Universitas Udayana, Bali, Indonesia
Biochemistry, Genetics & Molecular Biology Economics, Econometrics & Finance Health Professions Medicine & Pharmacology Nursing Public Health

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Myoepithelial carcinoma of lacrimal gland in HIV patient: A rare case L.P. Suryantini Septia Dewi; Putu Yuliawati; made laksmiNi Made Laksmi Utari; sukartiniA.A.A. Sukartini Djelantik
Intisari Sains Medis Vol. 13 No. 2 (2022): (In Press : 1 August 2022)
Publisher : DiscoverSys Inc.

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (757.343 KB) | DOI: 10.15562/ism.v13i2.1367

Abstract

Introduction: Lacrimal gland tumors have 1: 1,000,000 cases per year, accounting for one-fourth of lesions that occupy the orbital space. The rarity of lacrimal gland tumors and the many types of tumors with various types of lesions make determining optimal treatment difficult. A myoepithelial tumor is a rare epithelial neoplasm of the lacrimal gland. This paper aims to report a good outcome case of myoepithelial carcinoma. Case Report: A 30-year-old male complained of protruding his left eye since 2014, accompanied by pain and clear white discharge. The vision was getting blurry and also double vision. Patients with Human Immunodeficiency Virus (HIV) disease since 2013 on Anti Retro Viral (ARV) therapy. Right eye visual acuity was 6 / 7.5, and good eyeball examination. The left eye was 6/10 with no pinhole improvement, non-axial proptosis, and superolateral mass. The movement of his left eye was restricted. Other anterior and posterior segments were promising. The patient was diagnosed with pseudotumor and was given oral methylprednisolone. The eye condition is said to be getting better. The patient complained that the left eye was more prominent and protruding three years later, with blurred vision accompanied by infection. Left eye visual acuity becomes Light Perception Bad Projection with non-axial proptosis, retraction of palpebra and pus. Orbital exenteration was performed, and anatomical pathology examination revealed myoepithelial carcinoma of the lacrimal gland. The patient was planned for radiotherapy. Conclusion: These rare cases have made setting up a regimen in randomized controlled trials difficult. The rapid development of therapy gives more hope to treating patients with lacrimal gland tumors.
Exploring the Intricacies of Carotid Cavernous Fistula: A Case Series: Poster Presentation - Case Series - Resident SAPHIRA EVANI; PUTU YULIAWATI; NI MADE LAKSMI UTARI
Majalah Oftalmologi Indonesia Vol 49 No S2 (2023): Supplement Edition
Publisher : The Indonesian Ophthalmologists Association (IOA, Perhimpunan Dokter Spesialis Mata Indonesia (Perdami))

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35749/876jnv84

Abstract

Introduction : Carotid cavernous fistula (CCF) is caused by an abnormal connection between the carotid artery and the cavernous sinus, which can lead to eye-related problems. It is crucial to recognize its signs, as they can resemble other conditions. Case Illustration : First patient is a male 3-month-old baby, with unilateral right eye proptosis that was observed soon after birth and history of hypothyroid. Proptosis is more prominent while the baby is crying. Orbital ultrasonography revealed ophthalmica vein dilatation with S configuration, complex flow, and velocity of 10 cm/s. Second case is a 50-year-old male also with unilateral proptosis and orbital bruit with history of head trauma 2 months prior to admission. Patient came with complain of sudden blurry vision for 1 week. The results of the magnetic resonance venogram revealed tortuos dilated superior ophthalmica (SOV), cavernous sinus bulging, and dilated superior petrosal, sigmoid, transverse sinus, and internal jugular vein. Discussion : CCFs can occur at any age, but are more common between 40-60. Risk factors like head trauma, hypertension, connective tissue disorders increase the likelihood of developing CCF. They are often misdiagnosed as other conditions such as thyroid ophthalmopathy or conjunctivitis. Ocular doppler ultrasound can detect SOV dilation and arterial flow, while magnetic resonance imaging can show superior ophthalmic vein engorgement, muscle hypertrophy, and cavernous sinus dilatation. Treatment for symptomatic CCFs involves endovascular obliteration using balloons, embolic agents, or metallic coils, while asymptomatic and mildly symptomatic patients can be treated conservatively. Conclusion : Awareness of CCF symptoms, varied workup, prompt treatment is important to prevent severe complications.
Management of Lateral Canthal Coloboma in Goldenhar Syndrome: A Rare Case Report: Poster Presentation - Case Report - Resident KETUT PRAMANA ADIPUTRA; PUTU YULIAWATI; NI MADE LAKSMI UTARI
Majalah Oftalmologi Indonesia Vol 49 No S2 (2023): Supplement Edition
Publisher : The Indonesian Ophthalmologists Association (IOA, Perhimpunan Dokter Spesialis Mata Indonesia (Perdami))

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35749/nkkfz643

Abstract

Introduction : Goldenhar syndrome is a rare congenital disorder characterized by a wide range of physical anomalies affecting the face, ears, eyes, and spine. Case Illustration : Patient, female 19-year-old, complained of growing mass and blurry vision on right eye since childhood. The patient also has an asymetric face with the right side being smaller then left. She also has hearing disorder on her right ear. Ophthalmology examination revealed right eye's visual acuity is 6/120, lateral canthus coloboma , trichiasis and mass on the inferior palpebral, and conjunctiva attached to the cornea. Left eye is within normal limit. The right ear appears deformed, with no ear canal and preauricular skin tags. Patient underwent conjungtiva tumor excision and given labia mucosa graft with canthoplasty. Histology examination revealed benign lipomatous tumor. Patient feels more confident after oculoplasty surgery. Discussion : Goldenhar syndrome is a rare condition caused by abnormal development of the first and second branchial arches. It is characterized by a wide range of ocular features, including eyelid and iris coloboma, conjungtiva dermoid or dermolipoma, and more. Beside ocular features, other features are ear malformations, facial asymmetry, cleft lip or palate, and vertebral anomalies. It was unique case because an unformed canthus was found due to a large of conjunctival fornix mass. Appropriate management is necessary for a fulfilling life, though the disorder can have significant psychosocial effects. Conclusion : Goldenhar syndrome is a rare disease with numerous symptoms and its management is crucial for individuals to have a fulfilling life despite its potentially significant psychosocial impacts.
Management of Post Tumor Resection in Inferolateral Eyelid using Periosteal Flap and Canthoplasty Technique – A Case Report: Poster Presentation - Case Report - Resident CLARA VALENTINA; Putu Yuliawati; Ni Made Laksmi Utari
Majalah Oftalmologi Indonesia Vol 49 No S2 (2023): Supplement Edition
Publisher : The Indonesian Ophthalmologists Association (IOA, Perhimpunan Dokter Spesialis Mata Indonesia (Perdami))

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35749/vw8zen64

Abstract

Introduction : Eyelid defect repair goals are providing supportive connecting tissue and functional mucosal epithelium. Posterior lamellar reconstruction for tumor resection defect is still challenging. In this case, lower eyelid reconstruction can be accomplished by elevation and rotation of periosteal flap as posterior lamella. Case Illustration : A 68-years-old male came with inferolateral eyelid mass of Left Eye (LE) that was increasing in last 3 months. On LE examination found solitary cystic cutaneous lesion in inferior palpebra near lateral canthal, sized7x5mm, fixated, regular, and chewy consistency. Anterior of mass has same color as adjacent skin with hyperpigmentation lesion and posterior side was translucent with telangiectasia. He was suspected with LE ductal dd epidermoid cyst. Discussion : Periosteal flap and canthoplasty is procedure to repair inferolateral eyelid defect that are large to be closed primarily, however it requires adequate lateral canthal skin and tarsal plate. Posterior lamellais restored to create connective tissue framework, proper contour, and vertical canthal height. Tumor was removed and preperiosteal plan inferior to inferior orbital rim was dissected. The anterior lamella then transposed superiorly to make sure it will cover posterior lamellar reconstruction. Periosteal flap from lateral canthal tendon of infraorbital margin was harvested, flap was crossed to form sharp canthal angle and sutured to tarsal edges of lower eyelids as posterior lamella. A week later, LE showed natural contour and good function without eyelid malposition. Conclusion : Periosteal flap as posterior lamella reconstruction of eyelid defects is effective and efficient to repair eyelid defect due to its simplicity, reliability, and low risk complication.
GAMBARAN KELELAHAN MATA (ASTHENOPIA) PADA MAHASISWA PROGRAM STUDI SARJANA KEDOKTERAN FAKULTAS KEDOKTERAN UNIVERSITAS UDAYANA ANGKATAN 2018 SETELAH BERLAKUNYA KULIAH ONLINE REFAYANTI, NI MADE ERNITA; Laksmi Utari, Ni Made; Ayu Surasmiati, Ni Made; Eka Sutyawan, I Wayan; Sudarmaja, I Made
E-Jurnal Medika Udayana Vol 11 No 5 (2022): E-Jurnal Medika Udayana
Publisher : Universitas Udayana

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24843/MU.2022.V11.i05.P08

Abstract

Asthenopia tergolong kejadian yang sering terjadi yang dapat menyebabkan masalah kesehatan mata. Penelitian ini bertujuan untuk mengetahui angka prevalensi dan gambaran kelelahan mata (asthenopia) pada mahasiswa Program Studi Sarjana Kedokteran Fakultas Kedokteran Universitas Udayana angkatan 2018 setelah berlakunya kuliah online. Metode yang digunakan pada penelitian ini adalah penelitian berjenis deskriptif analitik dengan rancangan cross-sectional, sebanyak 220 sampel. Pengambilan data pada penelitian ini dilakukan dengan cara menyebarkan kuisioner melalui google form. Dari 220 sampel didapatkan prevalensi kejadian asthenopia 98.18% dengan kejadian terbanyak adalah asthenopia ringan. Didapatkan perbedaan bermakna pada distribusi asthenopia berdasarkan jenis kelamin, penggunaan laptop atau komputer (p<0,05) dan tidak ditemukan perbedaan yang bermakna pada distribusi asthenopia berdasarkan penggunaan handphone (p?0,05). Penggunaan laptop atau komputer yang lebih dari 8 jam paling banyak ditemukan pada kejadian asthenopia sedang dan berat.
Co-Authors AA Mas Putrawati T, AA Mas Anak Agung Ayu Sukartini Djelantik Anak Agung Surya Nirmala Dewi Ari Andayani Ayu Surasmiati, Ni Made Christine Natalia Gunawan CLARA VALENTINA Dendy Pranata Purba Eka Sutyawan, I Wayan I Gusti Ayu Ratna Suryaningrum I Made Sudarmaja I Wayan Eka Sutyawan Ida Ayu Pertami Dewi, Ida Ayu KETUT PRAMANA ADIPUTRA L.P. Suryantini Septia Dewi Made Agus Kusumadjaja Made Ayu Hapsari Dwi Ambarini Ni Luh Putu Nurindah Sukmawati Ni Made Ayu Surasmiati Ni wayan Sedani, Ni wayan Putu Aryani Putu Yuliawati REFAYANTI, NI MADE ERNITA Rima Febry Lesmana SAPHIRA EVANI