Retinoblastoma history and symptoms: Difference between revisions
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**[[Retinoblastoma]] | **[[Retinoblastoma]] | ||
Clinical [[Features (pattern recognition)|features]] of retinoblatoma are approximately the same in variable studies and the common findings are as follow:<ref name="pmid24792399">{{cite journal |vauthors=Chebbi A, Bouguila H, Boussaid S, Ben Aleya N, Zgholi H, Malek I, Zeghal I, Nacef L |title=[Clinical features of retinoblastoma in Tunisia] |language=French |journal=J Fr Ophtalmol |volume=37 |issue=6 |pages=442–8 |date=June 2014 |pmid=24792399 |doi=10.1016/j.jfo.2014.01.009 |url=}}</ref><ref name="pmid14654593">{{cite journal |vauthors=Abramson DH, Beaverson K, Sangani P, Vora RA, Lee TC, Hochberg HM, Kirszrot J, Ranjithan M |title=Screening for retinoblastoma: presenting signs as prognosticators of patient and ocular survival |journal=Pediatrics |volume=112 |issue=6 Pt 1 |pages=1248–55 |date=December 2003 |pmid=14654593 |doi= |url=}}</ref><ref name="ShifaGezmu2017">{{cite journal|last1=Shifa|first1=Jemal Zeberga|last2=Gezmu|first2=Alemayehu Mekonnen|title=Presenting signs of retinoblastoma at a tertiary level teaching hospital in Ethiopia|journal=Pan African Medical Journal|volume=28|year=2017|issn=1937-8688|doi=10.11604/pamj.2017.28.66.11199}}</ref> | Clinical [[Features (pattern recognition)|features]] of retinoblatoma are approximately the same in variable studies and the common findings are as follow:<ref name="pmid24792399">{{cite journal |vauthors=Chebbi A, Bouguila H, Boussaid S, Ben Aleya N, Zgholi H, Malek I, Zeghal I, Nacef L |title=[Clinical features of retinoblastoma in Tunisia] |language=French |journal=J Fr Ophtalmol |volume=37 |issue=6 |pages=442–8 |date=June 2014 |pmid=24792399 |doi=10.1016/j.jfo.2014.01.009 |url=}}</ref><ref name="pmid14654593">{{cite journal |vauthors=Abramson DH, Beaverson K, Sangani P, Vora RA, Lee TC, Hochberg HM, Kirszrot J, Ranjithan M |title=Screening for retinoblastoma: presenting signs as prognosticators of patient and ocular survival |journal=Pediatrics |volume=112 |issue=6 Pt 1 |pages=1248–55 |date=December 2003 |pmid=14654593 |doi= |url=}}</ref><ref name="ShifaGezmu2017">{{cite journal|last1=Shifa|first1=Jemal Zeberga|last2=Gezmu|first2=Alemayehu Mekonnen|title=Presenting signs of retinoblastoma at a tertiary level teaching hospital in Ethiopia|journal=Pan African Medical Journal|volume=28|year=2017|issn=1937-8688|doi=10.11604/pamj.2017.28.66.11199}}</ref> | ||
*Abnormal appearance of the pupil(leukocoria, also known as amaurotic cat's [[Red reflex|eye reflex]]), (Please see below). | *Abnormal appearance of the [[pupil]] ([[leukocoria]], also known as amaurotic cat's [[Red reflex|eye reflex]]), (Please see below). | ||
*Deviation of look to one side ([[strabismus]]) (especially when the [[macula]] is involved) | *Deviation of look to one side ([[strabismus]]) (especially when the [[macula]] is involved) | ||
*[[Decreased visual acuity|Decreased visual acquity]] | *[[Decreased visual acuity|Decreased visual acquity]] | ||
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*[[Vomiting]] | *[[Vomiting]] | ||
*[[Headache]] | *[[Headache]] | ||
Patients with [[retinoblastoma]] may also present with delay in [[developmental milestones]] and [[intellectual disability]] which may be | Patients with [[retinoblastoma]] may also present with delay in [[developmental milestones]] and [[intellectual disability]] which may be perceived by their caregivers.<ref name="ClarkAvishay2015">{{cite journal|last1=Clark|first1=Robin D.|last2=Avishay|first2=Stefanie G.|title=Retinoblastoma: Genetic Counseling and Testing|year=2015|pages=77–88|doi=10.1007/978-3-662-43451-2_8}}</ref> | ||
*[[Intellectual disability]] may be the result of accompanying [[disease]] or with no clear reason. | *[[Intellectual disability]] may be the result of accompanying [[disease]] or with no clear reason. | ||
*[[13q deletion syndrome|Chromosome 13q14 deletion]] may cause [[retinoblastoma]] and [[intellectual disability]]. | *[[13q deletion syndrome|Chromosome 13q14 deletion]] may cause [[retinoblastoma]] and [[intellectual disability]]. | ||
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[[Category:Medicine]] | [[Category:Medicine]] | ||
[[Category:Oncology]] | [[Category:Oncology]] | ||
[[Category:Up-To-Date]] | [[Category:Up-To-Date]] | ||
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[[Category:Primary care]] | [[Category:Primary care]] | ||
[[Category:Surgery]] | [[Category:Surgery]] | ||
Revision as of 14:55, 17 June 2019
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Retinoblastoma Microchapters |
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Retinoblastoma history and symptoms On the Web |
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Risk calculators and risk factors for Retinoblastoma history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[3] Simrat Sarai, M.D. [4]
Overview
The hallmark of retinoblastoma is leukocoria which is an abnormal appearance of the retina as viewed through the pupil, also known as amaurotic cat's eye reflex. Other common symptoms include strabismus and proptosis. The clinical presentation depends on the stage of the disease.
History and ymptoms
History
History of a patient with retinoblastoma should be focused on the following factors:[1]
- Complete perinatal history including:
- Pregnancy complications
- Prematurity
- Birth weight
- Type of delivery
- Use of oxygen
- Personal history of:
- Malformations
- Exposure to pets
- Recent trauma
- Systemic illness
- Family history of:
Clinical features of retinoblatoma are approximately the same in variable studies and the common findings are as follow:[2][3][4]
- Abnormal appearance of the pupil (leukocoria, also known as amaurotic cat's eye reflex), (Please see below).
- Deviation of look to one side (strabismus) (especially when the macula is involved)
- Decreased visual acquity
- Painful red eye
- Loss of vision
Presenting symptoms in adult onset of the tumor are insidious and are such as:[5]
- Dimness of vision
- Perception of floater
- Pain and redness
Advanced and/or metastatic form of the tumor also presents with constitutional symptoms such as:
Patients with retinoblastoma may also present with delay in developmental milestones and intellectual disability which may be perceived by their caregivers.[7]
- Intellectual disability may be the result of accompanying disease or with no clear reason.
- Chromosome 13q14 deletion may cause retinoblastoma and intellectual disability.
- Retinoblastoma has been also reported in a patient with Fragile x syndrome.
References
- ↑ Shields CL, Shields JA, Baez K, Cater JR, De Potter P (February 1994). "Optic nerve invasion of retinoblastoma. Metastatic potential and clinical risk factors". Cancer. 73 (3): 692–8. PMID 8299091.
- ↑ Chebbi A, Bouguila H, Boussaid S, Ben Aleya N, Zgholi H, Malek I, Zeghal I, Nacef L (June 2014). "[Clinical features of retinoblastoma in Tunisia]". J Fr Ophtalmol (in French). 37 (6): 442–8. doi:10.1016/j.jfo.2014.01.009. PMID 24792399.
- ↑ Abramson DH, Beaverson K, Sangani P, Vora RA, Lee TC, Hochberg HM, Kirszrot J, Ranjithan M (December 2003). "Screening for retinoblastoma: presenting signs as prognosticators of patient and ocular survival". Pediatrics. 112 (6 Pt 1): 1248–55. PMID 14654593.
- ↑ Shifa, Jemal Zeberga; Gezmu, Alemayehu Mekonnen (2017). "Presenting signs of retinoblastoma at a tertiary level teaching hospital in Ethiopia". Pan African Medical Journal. 28. doi:10.11604/pamj.2017.28.66.11199. ISSN 1937-8688.
- ↑ Khetan, Vikas; Sengupta, Sabyasachi; Pan, Utsab (2016). "Adult onset retinoblastoma". Indian Journal of Ophthalmology. 64 (7): 485. doi:10.4103/0301-4738.190099. ISSN 0301-4738.
- ↑ Image courtesy of Dr. Frank Gaillard Radiopaedia (original file [1]).[http://radiopaedia.org/licence Creative Commons BY-SA-NC
- ↑ Clark, Robin D.; Avishay, Stefanie G. (2015). "Retinoblastoma: Genetic Counseling and Testing": 77–88. doi:10.1007/978-3-662-43451-2_8.