International Journal of Science and Research (IJSR)

International Journal of Science and Research (IJSR)
Call for Papers | Fully Refereed | Open Access | Double Blind Peer Reviewed

ISSN: 2319-7064


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Case Studies | Paediatrics | India | Volume 11 Issue 6, June 2022 | Popularity: 4.6 / 10


     

Terson Syndrome - A Rare Presentation of Acute Lymphoblastic Leukaemia in Children

Tanveer Begum, Giridharan, Mohanchandran Chinnathambi Narayanan, B Anjaiah


Abstract: Acute lymphoblastic leukaemia arising from lymphoid precursor cells of the bone marrow, the lymphoreticular system, and the soft tissue can present with medullary and extramedullary involvement. Extramedullary involvement can affect any organ. Presentation with loss of vision secondary to bilateral vitreous haemorrhage along with intracerebral haemorrhage known as Terson syndrome is rare. There are case reports of such presentations in adults but, only a few in children. Here we are presenting a case of a 3year old male child who had bilateral visual loss secondary to vitreous haemorrhage along with intracerebral bleed, who was later diagnosed to have ALL and we want to give a brief overview of the literature about this unusual entity. Rapid investigation and timely initiation of treatment are needed to salvage the eye and the vision. Conclusion: Every child with acute lymphoblastic leukaemia with involvement of the brain should have at least one ophthalmologic examination.


Keywords: acute lymphoblastic leukaemia, extramedullary involvement, vitreous haemorrhage, intracerebral bleed, Terson syndrome


Edition: Volume 11 Issue 6, June 2022


Pages: 1595 - 1597


DOI: https://www.doi.org/10.21275/SR22623143819



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Tanveer Begum, Giridharan, Mohanchandran Chinnathambi Narayanan, B Anjaiah, "Terson Syndrome - A Rare Presentation of Acute Lymphoblastic Leukaemia in Children", International Journal of Science and Research (IJSR), Volume 11 Issue 6, June 2022, pp. 1595-1597, URL: https://www.ijsr.net/getabstract.php?paperid=SR22623143819, DOI: https://www.doi.org/10.21275/SR22623143819



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