Teratoma natural history: Difference between revisions
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==Overview== | ==Overview== | ||
The prognosis of teratoma depends on the type of tumor and malignant transformation. Mature teratoma is begnin and has an excellent prognosis compared to immature teratoma which has a favorable prognosis.The 6 year survival rate of patients with mature teratoma is approximately 96%. The overall 5 years survival rate of patient with immature teratoma is 90% and 75% for stage | The prognosis of teratoma depends on the type of tumor and malignant transformation. Mature teratoma is begnin and has an excellent prognosis compared to immature teratoma which has a favorable prognosis.The 6 year survival rate of patients with mature teratoma is approximately 96%. The overall 5 years survival rate of patient with immature teratoma is 90% and 75% for stage II-IV.Common complications are malignant transformation, rupture, torsion, and hemolytic anemia. | ||
==Natural History, Complications, and Prognosis== | ==Natural History, Complications, and Prognosis== | ||
===Natural History=== | ===Natural History=== | ||
*The symptoms of | *The symptoms of teratoma depends on the locations of the tumors. | ||
===Complications=== | ===Complications=== | ||
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===Prognosis=== | ===Prognosis=== | ||
* | *Mature teratoma has an excellent prognosis.<ref name="pmid25631333">{{cite journal| author=Terenziani M, D'Angelo P, Inserra A, Boldrini R, Bisogno G, Babbo GL et al.| title=Mature and immature teratoma: A report from the second Italian pediatric study. | journal=Pediatr Blood Cancer | year= 2015 | volume= 62 | issue= 7 | pages= 1202-8 | pmid=25631333 | doi=10.1002/pbc.25423 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25631333 }} </ref> | ||
* | *The 6 year survival rate of patients with mature teratoma is approximately 96%.<ref name="pmid9607423">{{cite journal| author=Göbel U, Calaminus G, Engert J, Kaatsch P, Gadner H, Bökkerink JP et al.| title=Teratomas in infancy and childhood. | journal=Med Pediatr Oncol | year= 1998 | volume= 31 | issue= 1 | pages= 8-15 | pmid=9607423 | doi=10.1002/(sici)1096-911x(199807)31:1<8::aid-mpo2>3.0.co;2-h | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9607423 }} </ref> | ||
*Immature teratoma has favorable prognosis for stage I and poor for advance stages.<ref name="pmid18541896">Mann JR, Gray ES, Thornton C, Raafat F, Robinson K, Collins GS et al. (2008) [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=18541896 Mature and immature extracranial teratomas in children: the UK Children's Cancer Study Group Experience.] ''J Clin Oncol'' 26 (21):3590-7. [http://dx.doi.org/10.1200/JCO.2008.16.0622 DOI:10.1200/JCO.2008.16.0622] PMID: [https://pubmed.gov/18541896 18541896]</ref> | |||
*[ | *Immature teratoma has 90%-95% of 5 years of survival rate for stage I and 75 % for stage II-IV.<ref name="pmid18541896">Mann JR, Gray ES, Thornton C, Raafat F, Robinson K, Collins GS et al. (2008) [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=18541896 Mature and immature extracranial teratomas in children: the UK Children's Cancer Study Group Experience.] ''J Clin Oncol'' 26 (21):3590-7. [http://dx.doi.org/10.1200/JCO.2008.16.0622 DOI:10.1200/JCO.2008.16.0622] PMID: [https://pubmed.gov/18541896 18541896]</ref> | ||
==References== | ==References== |
Latest revision as of 20:35, 25 November 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Gertrude Djouka, M.D.[2]
Overview
The prognosis of teratoma depends on the type of tumor and malignant transformation. Mature teratoma is begnin and has an excellent prognosis compared to immature teratoma which has a favorable prognosis.The 6 year survival rate of patients with mature teratoma is approximately 96%. The overall 5 years survival rate of patient with immature teratoma is 90% and 75% for stage II-IV.Common complications are malignant transformation, rupture, torsion, and hemolytic anemia.
Natural History, Complications, and Prognosis
Natural History
- The symptoms of teratoma depends on the locations of the tumors.
Complications
- Common complications of teratoma specially ovarian teratoma include:[1][2][3]
- Torsion
- Rupture
- Malignant transformation
- Infections
- Autoimmune hemolytic anemia
Prognosis
- Mature teratoma has an excellent prognosis.[4]
- The 6 year survival rate of patients with mature teratoma is approximately 96%.[5]
- Immature teratoma has favorable prognosis for stage I and poor for advance stages.[6]
- Immature teratoma has 90%-95% of 5 years of survival rate for stage I and 75 % for stage II-IV.[6]
References
- ↑ Park SB, Kim JK, Kim KR, Cho KS (2008). "Imaging findings of complications and unusual manifestations of ovarian teratomas". Radiographics. 28 (4): 969–83. doi:10.1148/rg.284075069. PMID 18635624.
- ↑ Comerci JT, Licciardi F, Bergh PA, Gregori C, Breen JL (1994) Mature cystic teratoma: a clinicopathologic evaluation of 517 cases and review of the literature. Obstet Gynecol 84 (1):22-8. PMID: 8008317
- ↑ Singh P, Yordan EL, Wilbanks GD, Miller AW, Wee A (1988). "Malignancy associated with benign cystic teratomas (dermoid cysts) of the ovary". Singapore Med J. 29 (1): 30–4. PMID 2841767.
- ↑ Terenziani M, D'Angelo P, Inserra A, Boldrini R, Bisogno G, Babbo GL; et al. (2015). "Mature and immature teratoma: A report from the second Italian pediatric study". Pediatr Blood Cancer. 62 (7): 1202–8. doi:10.1002/pbc.25423. PMID 25631333.
- ↑ Göbel U, Calaminus G, Engert J, Kaatsch P, Gadner H, Bökkerink JP; et al. (1998). "Teratomas in infancy and childhood". Med Pediatr Oncol. 31 (1): 8–15. doi:10.1002/(sici)1096-911x(199807)31:1<8::aid-mpo2>3.0.co;2-h. PMID 9607423.
- ↑ 6.0 6.1 Mann JR, Gray ES, Thornton C, Raafat F, Robinson K, Collins GS et al. (2008) Mature and immature extracranial teratomas in children: the UK Children's Cancer Study Group Experience. J Clin Oncol 26 (21):3590-7. DOI:10.1200/JCO.2008.16.0622 PMID: 18541896