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Primary orbital rhabdoid tumour masquerading as atypical persistent foetal vasculature.
Douch, Catherine; Merve, Ashirwad; Mankad, Kshitij; Jorgensen, Mette.
Affiliation
  • Douch C; Neonatal Unit, Chelsea and Westminster Healthcare NHS Trust, London, UK c.douch@nhs.net.
  • Merve A; Neuropathology, Great Ormond Street Hospital for Children, London, UK.
  • Mankad K; Neuroradiology, Great Ormond Street Hospital for Children, London, UK.
  • Jorgensen M; Oncology, Great Ormond Street Hospital for Children, London, UK.
BMJ Case Rep ; 17(1)2024 Jan 09.
Article in En | MEDLINE | ID: mdl-38195193
ABSTRACT
We present a case of primary rhabdoid tumour of the orbit. Presenting features at birth included congenital ptosis, conjunctival injection, hyphaema and microphthalmia. The unique presentation caused a late diagnosis following the development of rapid proptosis 6 months later. We suggest that orbital rhabdoid tumour be considered in the differential diagnoses of patients presenting with atypical persistent foetal vasculature features.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Orbital Neoplasms / Exophthalmos / Microphthalmos / Rhabdoid Tumor / Persistent Hyperplastic Primary Vitreous Type of study: Diagnostic_studies / Etiology_studies Limits: Humans / Infant Language: En Journal: BMJ Case Rep Year: 2024 Document type: Article Affiliation country: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Orbital Neoplasms / Exophthalmos / Microphthalmos / Rhabdoid Tumor / Persistent Hyperplastic Primary Vitreous Type of study: Diagnostic_studies / Etiology_studies Limits: Humans / Infant Language: En Journal: BMJ Case Rep Year: 2024 Document type: Article Affiliation country: Reino Unido