Primary orbital yolk sac tumour in a 14-year-old girl

Zubair Ahmad1, Amna Khurshid, Asim Qureshi

  • 1Aga Kahn University, Stadium Road Karachi, Karachi, 74800, Pakistan.

BMJ Case Reports
|November 19, 2011
PubMed

Insights

A rare yolk sac tumor, a type of germ cell tumor, was found in the orbit of a 14-year-old girl. This case highlights an unusual presentation of this common infant cancer.

Area of Science:

  • Oncology
  • Ophthalmology
  • Pathology

Background:

  • Yolk sac tumors are common malignant germ cell tumors typically found in infants' testes or ovaries.
  • Extragonadal yolk sac tumors can occur in various locations, with head and neck sites accounting for 5% of all germ cell tumors.
  • Primary yolk sac tumors of the orbit are exceptionally rare.

Purpose of the Study:

  • To report an extremely rare case of a primary yolk sac tumor originating in the orbit.
  • To describe the clinical presentation and extent of an orbital yolk sac tumor in a pediatric patient.
  • To contribute to the understanding of extragonadal germ cell tumors in unusual locations.

Main Methods:

  • Case report detailing a 14-year-old female patient.
  • Clinical and radiological evaluation of an orbital mass.
  • Histopathological confirmation of yolk sac tumor.

Main Results:

  • A primary yolk sac tumor was identified in the orbit of a 14-year-old girl.
  • The tumor demonstrated invasion into the periorbital and intracranial spaces.
  • This represents an extremely unusual site for a primary yolk sac tumor.

Conclusions:

  • Orbital yolk sac tumors are exceedingly rare but must be considered in the differential diagnosis of orbital masses in children.
  • Early diagnosis and appropriate management are crucial for extragonadal germ cell tumors, even in unusual locations.
  • This case underscores the importance of comprehensive evaluation for rare tumor presentations.

Related Concept Videos