Displaying all 6 publications

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  1. Kah TA, Annuar FH
    N Engl J Med, 2012 Jul 19;367(3):258.
    PMID: 22808961 DOI: 10.1056/NEJMicm1112964
    Matched MeSH terms: Eye Neoplasms/diagnosis*
  2. Sukumaran DO
    Med J Malaysia, 1991 Jun;46(2):129-35.
    PMID: 1839416
    Retinoblastoma was clinically diagnosed in 38 patients in the University Hospital between 1968 to 1988. White pupil or cat's eye reflex, found in 25 patients, was the most common symptom. Four patients refused any form of treatment. Of the 27 histopathologically confirmed cases, 16 were males and 11 were females. There was no ethnic group predominance, although a male preponderance was observed among Malay patients (M:F 3:1, p less than 0.05). Treatment in cases with unilateral disease, without extra ocular extension consisted of enucleation of the involved eye, with close examination of the contralateral eye in follow-up. In cases presenting with bilateral tumour the worse eye was removed. Of 20 cases of histopathologically proven unilateral retinoblastoma treated surgically, 12 patients survived for a mean period of 4.5 years (Range: 1-19 years). The defaulter rate for this group of patients was 55%. None of the 7 cases of bilateral retinoblastoma survived beyond 5 years (Mean survival 2.5 years).
    Matched MeSH terms: Eye Neoplasms/diagnosis*
  3. Ramlee N, Ramli N, Tajudin LS
    Orbit, 2007 Jun;26(2):137-9.
    PMID: 17613864
    We reported a case of pleomorphic adenoma of the lacrimal gland involving the palpebral lobe in young teenage girl of Asian origin. The presentation at young age group is rare, which initially misdiagnosed as a large chalazion. The benign tumor with its intact pseudocapsule was removed through lateral orbitotomy together with the suspicious looking orbital lobe.
    Matched MeSH terms: Eye Neoplasms/diagnosis*
  4. Wahab NA, Ramasamy U, George J, Madhavan M, Arif AR, Abdullah J
    Med J Malaysia, 2006 Dec;61(5):641-3.
    PMID: 17623971 MyJurnal
    We report a case of an adult who presented with progressive swelling in the right eye with suggestive of intracranial lesion on imaging. Histopathological revealed a lacrimal gland malignant mixed tumour.
    Matched MeSH terms: Eye Neoplasms/diagnosis
  5. Maharajah KR, Hussein A, Mohamad H, Khan SA, At LS
    Orbit, 2009;28(5):306-8.
    PMID: 19874126 DOI: 10.3109/01676830903044346
    We report a case of primary non-Hodgkins lymphoma of the lacrimal sac in a 60-year-old Asian lady, who presented with persistent epiphora and recurrent medial canthal swelling. Primary lymphoma of the lacrimal sac is rare and it can be easily misdiagnosed. Delayed in diagnosis may be related to mortality. To minimize the risk of overlooking specific pathology it is important to assess the appearance of the lacrimal sac and its surrounding structures intraoperatively. Biopsy of the lacrimal sac is required in cases where specific pathology is suspected.
    Matched MeSH terms: Eye Neoplasms/diagnosis*
  6. Tengku-Fatishah A, Abdullah B, Sanjeevan N, Nurul-Shuhada AH, Sharifah-Emilia TS, Haron J, et al.
    Can J Ophthalmol, 2019 08;54(4):e196-e199.
    PMID: 31358169 DOI: 10.1016/j.jcjo.2018.10.006
    Matched MeSH terms: Eye Neoplasms/diagnosis*
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