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  1. Article ; Online: Venous malformation of the conjunctiva and orbit.

    Devaraj, Athira / Gera, Pratik / Swathi, S / Kasturi, Nirupama

    Indian journal of pathology & microbiology

    2023  Volume 66, Issue 2, Page(s) 379–381

    Abstract: A 28-year-old male presented with a large conjunctival lobulated, nonpulsatile, red vascular lesion involving a large part of the temporal quadrant of the left globe. There was no proptosis or globe displacement, but the left eye abduction was limited. ... ...

    Abstract A 28-year-old male presented with a large conjunctival lobulated, nonpulsatile, red vascular lesion involving a large part of the temporal quadrant of the left globe. There was no proptosis or globe displacement, but the left eye abduction was limited. T2-weighted magnetic resonance imaging scan of the brain and orbit revealed an extensive contrast-enhancing lobulated lesion in the left half of the face involving the upper lip, cheek, oral cavity, extraconal space of left orbit, and nasal cavity. He underwent surgical excision of the conjunctival lesion with amniotic membrane reconstruction.
    MeSH term(s) Male ; Humans ; Adult ; Orbit/diagnostic imaging ; Orbit/surgery ; Orbit/pathology ; Exophthalmos/etiology ; Exophthalmos/pathology ; Conjunctiva/surgery ; Cheek
    Language English
    Publishing date 2023-04-18
    Publishing country India
    Document type Case Reports
    ZDB-ID 197621-7
    ISSN 0974-5130 ; 0377-4929
    ISSN (online) 0974-5130
    ISSN 0377-4929
    DOI 10.4103/ijpm.ijpm_490_21
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: An uncommon presentation of WAGR syndrome with persistent fetal vasculature.

    Devaraj, Athira / Shetty, Shashikant / Patnaik, Nisheeta / Parida, Haemoglobin / Pandurangan, Sneha

    Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

    2023  Volume 27, Issue 6, Page(s) 357–359

    Abstract: Aniridia is an autosomal dominant congenital malformation associated with mutations in the PAX6 gene. It can be associated with deletion in the contiguous WT1 gene, leading to WAGR syndrome, characterized by Wilm tumor, aniridia, genitourinary anomalies, ...

    Abstract Aniridia is an autosomal dominant congenital malformation associated with mutations in the PAX6 gene. It can be associated with deletion in the contiguous WT1 gene, leading to WAGR syndrome, characterized by Wilm tumor, aniridia, genitourinary anomalies, and mental retardation. Persistent fetal vasculature is a developmental malformation caused by incomplete regression of hyaloid vasculature. Most cases of persistent fetal vasculature occur sporadically; however, some inherited forms are described. We report a case of genetically confirmed WAGR associated with congenital cataract and persistent fetal vasculature.
    MeSH term(s) Humans ; WAGR Syndrome/diagnosis ; WAGR Syndrome/genetics ; WAGR Syndrome/pathology ; Chromosome Deletion ; Aniridia/diagnosis ; Aniridia/genetics ; Aniridia/pathology ; Intellectual Disability/genetics ; Mutation
    Language English
    Publishing date 2023-09-23
    Publishing country United States
    Document type Case Reports
    ZDB-ID 1412476-2
    ISSN 1528-3933 ; 1091-8531
    ISSN (online) 1528-3933
    ISSN 1091-8531
    DOI 10.1016/j.jaapos.2023.07.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Wetlab training during COVID-19 era; an ophthalmology resident's perspective.

    Devaraj, Athira / Satheesh, Aswathi Neena / Panicker, Gayathri J / Kaliyaperumal, Subashini

    Indian journal of ophthalmology

    2020  Volume 69, Issue 1, Page(s) 158–159

    MeSH term(s) COVID-19/epidemiology ; Education, Medical/methods ; Humans ; Internship and Residency/methods ; Ophthalmology/education ; Pandemics
    Language English
    Publishing date 2020-12-15
    Publishing country India
    Document type Letter
    ZDB-ID 187392-1
    ISSN 1998-3689 ; 0301-4738
    ISSN (online) 1998-3689
    ISSN 0301-4738
    DOI 10.4103/ijo.IJO_3496_20
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Conjunctival Trichodiscoma of the Lower Eyelid.

    Kasturi, Nirupama / Chavhan, Pratima / Ramakant, Ghag Gaurav / Devaraj, Athira / Babu K, Ramesh / N G, Rajesh

    Ophthalmic plastic and reconstructive surgery

    2019  Volume 35, Issue 6, Page(s) e145–e147

    Abstract: Trichodiscomas are benign tumors of the skin which develop around a hair follicle. They usually present on the face, neck, or trunk region. The authors report a rare case of a 63-year-old man who presented with a tumor on the left lower eyelid that was ... ...

    Abstract Trichodiscomas are benign tumors of the skin which develop around a hair follicle. They usually present on the face, neck, or trunk region. The authors report a rare case of a 63-year-old man who presented with a tumor on the left lower eyelid that was histologically proven to be a trichodiscoma of conjunctival origin.Trichodiscomas are benign tumors of the skin appendage which develop around a hair follicle. Although conjunctival hair follicles are rudimentary and do not give rise to hair, rarely a benign proliferation of these cells can result in trichodiscoma of the conjunctiva.
    MeSH term(s) Conjunctiva/pathology ; Eyelid Neoplasms/pathology ; Hamartoma/pathology ; Humans ; Male ; Middle Aged ; Skin Neoplasms/pathology
    Language English
    Publishing date 2019-09-30
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 632830-1
    ISSN 1537-2677 ; 0740-9303
    ISSN (online) 1537-2677
    ISSN 0740-9303
    DOI 10.1097/IOP.0000000000001470
    Database MEDical Literature Analysis and Retrieval System OnLINE

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