Trilateral retinoblastoma

From WikiMD.org
Jump to navigation Jump to search

Trilateral Retinoblastoma

Trilateral retinoblastoma (/traɪˈlætərəl ˌrɛtɪnoʊblæˈstoʊmə/) is a rare form of retinoblastoma, a type of cancer that begins in the retina, the sensitive lining on the inside of the eye.

Etymology

The term "trilateral" comes from the Latin "tri-" meaning "three" and "lateral" meaning "side". "Retinoblastoma" is derived from "retino-", referring to the retina, and "-blastoma", a suffix used in pathological terms to denote a cancer comprising immature cells.

Definition

Trilateral retinoblastoma is characterized by the presence of bilateral retinoblastoma (cancer in both eyes) along with an intracranial neuroblastic tumor, typically in the pineal gland or less commonly, the suprasellar or parasellar region. This third tumor gives the condition its name.

Related Terms

See Also

References

  • Shields, C. L., et al. (2009). "Clinical spectrum and prognosis of pineal parenchymal tumors in 42 cases." Journal of Neurosurgery Pediatrics 3(3): 206-212.
  • De Potter, P., et al. (1994). "Clinical predictive factors for development of bilateral retinoblastoma." Ophthalmology 101(12): 1895-1900.

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski