Difference between revisions of "Retinoblastoma"

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   MeshID        = D012175 |
 
   MeshID        = D012175 |
 
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'''Retinoblastoma''' is a [[cancer]] of the [[retina]].  Development of this tumor is initiated by [[mutation]]s<ref>{{cite journal |author=Knudson A |title=Mutation and cancer: statistical study of retinoblastoma |journal=Proc Natl Acad Sci U S A |volume=68 |issue=4 |pages=820-3 |year=1971 |pmid=5279523}}</ref> that inactivate both copies of the ''[[RB1]]'' gene, which codes for the [[retinoblastoma protein]].<ref>{{cite journal |author=Friend S, Bernards R, Rogelj S, Weinberg R, Rapaport J, Albert D, Dryja T |title=A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma |journal=Nature |volume=323 |issue=6089 |pages=643-6 |year= |pmid=2877398}}</ref>
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'''Retinoblastoma''' is a [[cancer]] of the [[retina]].  Development of this tumor is initiated by [[mutation]]s<ref>{{cite journal |author=Knudson A |title=Mutation and cancer: statistical study of retinoblastoma |journal=Proc Natl Acad Sci U S A |volume=68 |issue=4 |pages=820-3 |year=1971 |pmid=5279gadgqetqer523}}</ref> that inactivate both copies of the ''[[RB1]]'' gene, which codes for the [[retinoblastoma protein]].<ref>{{cite journal |author=Friend S, Bernards R, Rogelj S, Weinberg R, Rapaport J, Albert D, Dryja T |title=A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma |journal=Nature |volume=323 |issue=6089 |pages=643-6 |year= |pmid=2877398}}</ref>
  
 
It occurs mostly in children younger than 5 years and accounts for about 3% of the cancers occurring in children younger than 15 years. Adult cases have also been clinically recorded.<ref>{{cite journal |author=Takahashi T, Tamura S, Inoue M, Isayama Y, Sashikata T |title=Retinoblastoma in a 26-year-old adult |journal=Ophthalmology |volume=90 |issue=2 |pages=179-83 |year=1983 |pmid=6856254}}</ref> The estimated annual incidence is approximately 4 per million children.<ref>[http://www.cancer.org/docroot/CRI/content/CRI_2_4_1X_What_are_the_key_statistics_for_retinoblastoma_37.asp?sitearea= cancer.org]</ref>  It begins with white blotches in one or both eyes ([[leukocoria]]) which can be seen in [[photograph]]s (this is distinct from the [[red-eye effect]] which is normal); or when light reflects off the eye, as when watching [[television]].
 
It occurs mostly in children younger than 5 years and accounts for about 3% of the cancers occurring in children younger than 15 years. Adult cases have also been clinically recorded.<ref>{{cite journal |author=Takahashi T, Tamura S, Inoue M, Isayama Y, Sashikata T |title=Retinoblastoma in a 26-year-old adult |journal=Ophthalmology |volume=90 |issue=2 |pages=179-83 |year=1983 |pmid=6856254}}</ref> The estimated annual incidence is approximately 4 per million children.<ref>[http://www.cancer.org/docroot/CRI/content/CRI_2_4_1X_What_are_the_key_statistics_for_retinoblastoma_37.asp?sitearea= cancer.org]</ref>  It begins with white blotches in one or both eyes ([[leukocoria]]) which can be seen in [[photograph]]s (this is distinct from the [[red-eye effect]] which is normal); or when light reflects off the eye, as when watching [[television]].
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==Treatment==
 
==Treatment==
Until recently the only treatment was to remove the affected eyeball before the cancer spread. [[Enucleation]] is still the treatment of choice for most unilateral cases. Affected children in developing countries present with advanced features and usually die of metastatic spread. In its initial stages, retinoblastoma is very similar to [[Coats disease]], a non-cancerous retina disease. Coats' Disease should be ruled out before enucleation is done. A mis-diagnosis of Retinoblastoma accounts for the greatest number of Coats' disease eyes being enucleated.  
+
Until recently the only treatment was to remove the affected eyeball before the cancer spread. Chemotherapy is the treatment of choice for most unilateral cases. However with locally advanced disease external beam radiation may be needed and if both eyes are involved enucleation may be the only option. Affected children in developing countries present with advanced features and usually die of metastatic spread. In its initial stages, retinoblastoma is very similar to [[Coats disease]], a non-cancerous retina disease. Coats' Disease should be ruled out before enucleation is done. A mis-diagnosis of Retinoblastoma accounts for the greatest number of Coats' disease eyes being enucleated.  
  
 
Many children with bilateral retinoblastoma can be treated with a preservation attempt. Tumor [[chemotherapy|chemoreduction]] with [[carboplatin]] and other drugs may reduce the tumor volume making them amenable to local therapies <ref>{{cite journal |author=Dunkel IJ, Lee TC, Shi W, Beaverson KL, Novetsky D, Lyden D, Finlay JL, McCormick B, Abramson DH. |title=A phase II trial of carboplatin for intraocular retinoblastoma. |journal=Pediatr Blood Cancer. |pmid=17301956 }}</ref>
 
Many children with bilateral retinoblastoma can be treated with a preservation attempt. Tumor [[chemotherapy|chemoreduction]] with [[carboplatin]] and other drugs may reduce the tumor volume making them amenable to local therapies <ref>{{cite journal |author=Dunkel IJ, Lee TC, Shi W, Beaverson KL, Novetsky D, Lyden D, Finlay JL, McCormick B, Abramson DH. |title=A phase II trial of carboplatin for intraocular retinoblastoma. |journal=Pediatr Blood Cancer. |pmid=17301956 }}</ref>
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Local therapies include-
 
Local therapies include-
  
* [[Laser therapy]] (Uses infrared laser light to precisely destroy the blood vessels surrounding a tumor.)
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[[Laser therapy]] (Uses infrared laser light to precisely destroy the blood vessels surrounding a tumor.)
 
* [[Cryotherapy]] (use of a cold gas which is injected into the affected part of the retina to shrink the tumor.)
 
* [[Cryotherapy]] (use of a cold gas which is injected into the affected part of the retina to shrink the tumor.)
 
* [[Thermotherapy]] (A relatively new technique used mainly in new testing. It uses the principle that if heat is applied to the affected area, a tumor will sustain more damage than healthy cells because healthy cells can cool themselves better using healthy surrounding blood vessels. If this technique is not immediately successful it may increase the efficacy of other treatments such as chemotherapy and focused radiation plaques.)
 
* [[Thermotherapy]] (A relatively new technique used mainly in new testing. It uses the principle that if heat is applied to the affected area, a tumor will sustain more damage than healthy cells because healthy cells can cool themselves better using healthy surrounding blood vessels. If this technique is not immediately successful it may increase the efficacy of other treatments such as chemotherapy and focused radiation plaques.)

Revision as of 19:00, 15 October 2007

Retinoblastoma
Retinoblastoma.jpg
Leukocoria of right eye indicating presence of tumor
ICD-10 C69.2
ICD-9 190.5
ICD-O: M9510/3
OMIM 180200
DiseasesDB 11434
MedlinePlus 001030
eMedicine oph/346 
MeSH D012175

Retinoblastoma is a cancer of the retina. Development of this tumor is initiated by mutations[1] that inactivate both copies of the RB1 gene, which codes for the retinoblastoma protein.[2]

It occurs mostly in children younger than 5 years and accounts for about 3% of the cancers occurring in children younger than 15 years. Adult cases have also been clinically recorded.[3] The estimated annual incidence is approximately 4 per million children.[4] It begins with white blotches in one or both eyes (leukocoria) which can be seen in photographs (this is distinct from the red-eye effect which is normal); or when light reflects off the eye, as when watching television.

The tumor may begin in one or both eyes. Retinoblastoma is usually confined to the eye but can spread to the brain via the optic nerve.

As the retina is the light-sensitive part of the eye necessary for vision, loss of vision occurs.

The condition reached the headlines in May 2007, when Utah Jazz point guard Derek Fisher revealed that his 10-month-old daughter had the condition. Fisher missed Game 1 and half of Game 2 of the playoff series versus the Golden State Warriors to be with his daughter for her surgery in New York City.

Treatment

Until recently the only treatment was to remove the affected eyeball before the cancer spread. Chemotherapy is the treatment of choice for most unilateral cases. However with locally advanced disease external beam radiation may be needed and if both eyes are involved enucleation may be the only option. Affected children in developing countries present with advanced features and usually die of metastatic spread. In its initial stages, retinoblastoma is very similar to Coats disease, a non-cancerous retina disease. Coats' Disease should be ruled out before enucleation is done. A mis-diagnosis of Retinoblastoma accounts for the greatest number of Coats' disease eyes being enucleated.

Many children with bilateral retinoblastoma can be treated with a preservation attempt. Tumor chemoreduction with carboplatin and other drugs may reduce the tumor volume making them amenable to local therapies [5]

Local therapies include-

Laser therapy (Uses infrared laser light to precisely destroy the blood vessels surrounding a tumor.)

  • Cryotherapy (use of a cold gas which is injected into the affected part of the retina to shrink the tumor.)
  • Thermotherapy (A relatively new technique used mainly in new testing. It uses the principle that if heat is applied to the affected area, a tumor will sustain more damage than healthy cells because healthy cells can cool themselves better using healthy surrounding blood vessels. If this technique is not immediately successful it may increase the efficacy of other treatments such as chemotherapy and focused radiation plaques.)
  • Radiotherapy (Generally used as a last resort, radiotherapy was previously the treatment of choice before the above mentioned treatments were developed. Radiotherapy destroys cancerous growths using gamma radiation but it carries with it many drawbacks, including:-
    • Possibility of secondary cancerous growths which present themselves months or years later.
    • Destruction of healthy cells in the area surrounding the treated tumor.
    • Bone deformation due to the destruction of the growth plates mainly in the area of the temple.)

It is important that children with retinoblastoma are treated in specialist centers.

Brachytherapy with beta-emitting eye applicators have also been a successful major treatment. BEBIG (GmbH-Berlin-Germany) produces various kinds of ruthenium ophthalmic applicators for treating retinoblastoma.

See Ben Underwood for a case who compensated for the resulting blindness by developing human echolocation.

References

  1. Knudson A (1971). "Mutation and cancer: statistical study of retinoblastoma". Proc Natl Acad Sci U S A. 68 (4): 820–3. PMID 5279gadgqetqer523 Check |pmid= value (help).
  2. Friend S, Bernards R, Rogelj S, Weinberg R, Rapaport J, Albert D, Dryja T. "A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma". Nature. 323 (6089): 643–6. PMID 2877398.
  3. Takahashi T, Tamura S, Inoue M, Isayama Y, Sashikata T (1983). "Retinoblastoma in a 26-year-old adult". Ophthalmology. 90 (2): 179–83. PMID 6856254.
  4. cancer.org
  5. Dunkel IJ, Lee TC, Shi W, Beaverson KL, Novetsky D, Lyden D, Finlay JL, McCormick B, Abramson DH. "A phase II trial of carboplatin for intraocular retinoblastoma". Pediatr Blood Cancer. PMID 17301956.

See also

External links

de:Retinoblastom nl:Retinoblastoom fi:Retinoblastooma ur:شبکی ورمِ ارومہ


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