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Orbital leiomyoma presenting as inverse globe retraction syndrome: a unique presentation of a rare disease.
Panicker, Gayathri J; Nair A K, Preeta; Agarkar, Sumita; Nisar, Sonam Poonam; Joseph, Leena Dennis.
Afiliação
  • Panicker GJ; Pediatric Ophthalmology and Strabismus Services, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India.
  • Nair A K P; Orbit, Oculoplasty, Reconstructive and Aesthetic Services, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India.
  • Agarkar S; Pediatric Ophthalmology and Strabismus Services, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India. Electronic address: drsar@snmail.org.
  • Nisar SP; Orbit, Oculoplasty, Reconstructive and Aesthetic Services, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India.
  • Joseph LD; Department of Pathology, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India.
J AAPOS ; 27(2): 105-107, 2023 04.
Article em En | MEDLINE | ID: mdl-36739941
ABSTRACT
Inverse globe retraction syndrome is a rare ocular motility disorder characterized by limited abduction, with globe retraction and up- or downshoots on attempted abduction, differentiating it from globe retraction due to Duane retraction syndrome, seen on attempted adduction. It can be congenital or acquired. We report the case of a 3-year-old girl who presented with classical features of inverse globe retraction syndrome secondary to an underlying orbital tumor involving the medial rectus muscle. Incisional biopsy confirmed the diagnosis of a leiomyoma. At 10 months' follow-up, vision, ocular alignment, and ocular motility had improved.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Orbitárias / Síndrome da Retração Ocular / Leiomioma Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Orbitárias / Síndrome da Retração Ocular / Leiomioma Idioma: En Ano de publicação: 2023 Tipo de documento: Article