RSS-Feed abonnieren
DOI: 10.1055/s-0041-1740997
Recurrence and Metachronous Disease in Children with Benign Ovarian Tumors: A Systematic Review of the Literature
Abstract
Aim The majority of ovarian tumors in children are benign, with good prognosis following complete resection. Little is published on the incidence of tumor recurrence and metachronous disease, and follow-up management of children with benign ovarian tumors (BOTs) remains a matter of debate. This systematic review aimed to evaluate the incidence and timing of recurrence and metachronous disease in children with BOTs in pediatric literature.
Methods Comprehensive literature searches of the English literature (PubMed, OVID, EMBASE databases) from inception to present according to the Preferred Reporting Items for Systematic Review and Meta-analysis guidelines. Outcomes for tumor recurrence and metachronous disease were synthesized.
Results Nineteen studies comprising 1,069 patients with BOTs were included in the analysis. All studies were retrospective cohort studies of children less than 18 years old. A total of 56 events of recurrence or metachronous disease were reported in these patients. The overall risk of recurrence/metachronous event occurrence was 5.2%/2.9%. Seventy-five percent of events occurred within the first 4 years following resection.
Conclusion Although the studies identified are few and heterogeneous, they demonstrate a significant risk of tumor recurrence and metachronous disease for children following resection of a BOT.
Especially following total unilateral oophorectomy, these children are at risk of losing the contralateral ovary in case of metachronous disease.
Immediate discharge from follow-up, therefore, does not appear safe. The majority of events occurred within the first 4 years following resection. Follow-up for children following resection of a BOT should, therefore, be continued for a minimum of 4 years following surgery. Larger, long-term prospective studies are required to more accurately determine the true incidence and long-term outcomes for children and adolescents with these tumors.
Publikationsverlauf
Eingereicht: 09. Juli 2021
Angenommen: 18. November 2021
Artikel online veröffentlicht:
11. Januar 2022
© 2021. Thieme. All rights reserved.
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References
- 1 Skinner MA, Schlatter MG, Heifetz SA, Grosfeld JL. Ovarian neoplasms in children. Arch Surg 1993; 128 (08) 849-853 , discussion 853–854
- 2 Ulbright TM. Germ cell tumors of the gonads: a selective review emphasizing problems in differential diagnosis, newly appreciated, and controversial issues. Mod Pathol 2005; 18 (Suppl. 02) S61-S79
- 3 Braungart S, Craigie RJ, Farrelly P, Losty PD. CCLG Surgeons Collaborators. Ovarian tumors in children: how common are lesion recurrence and metachronous disease? A UK CCLG Surgeons Cancer Group nationwide study. J Pediatr Surg 2020; 55 (10) 2026-2029
- 4 Terenziani M, D'Angelo P, Inserra A. et al. Mature and immature teratoma: a report from the second Italian pediatric study. Pediatr Blood Cancer 2015; 62 (07) 1202-1208
- 5 Chabaud-Williamson M, Netchine I, Fasola S. et al. Ovarian-sparing surgery for ovarian teratoma in children. Pediatr Blood Cancer 2011; 57 (03) 429-434
- 6 Taskinen S, Urtane A, Fagerholm R, Lohi J, Taskinen M. Metachronous benign ovarian tumors are not uncommon in children. J Pediatr Surg 2014; 49 (04) 543-545
- 7 Childrens' Cancer and Leukaemia Group Germ Cell Tumour Group. Brougham M, Nicholson J, Stoneham S, Murray M, Hook L, Arul S. et al. Interim guideline for the treatment of extracranial germ cell tumours in children and adolescents. Accessed December 8, 2021: https://www.cclg.org.uk/write/MediaUploads/Member%20area/Treatment%20guidelines/614_Extracranial_GCT_Guidance_updated_June_2018.pdf
- 8 Braungart S, Craigie RJ, Losty PD. Controversies in the management of ovarian tumours in prepubertal children - a BAPS and UK CCLG Surgeons Cancer Group National Survey. J Pediatr Surg 2018; 53 (11) 2231-2234
- 9 Moher D, Liberati A, Tetzlaff J, Altman DG. PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ 2009; 339: b2535
- 10 Szymon O, Bogusz B, Taczanowska-Niemczuk A, Maślanka M, Górecki W. Ovarian sparing surgery in mature ovarian teratomas in children: a 20-year single-center experience. Eur J Pediatr Surg 2021; 31 (01) 2-7
- 11 Elgendy A, Lakshminarayanan B, Elrouby A. et al. Management of pediatric benign ovarian tumors in England and Egypt: a comparative study. Afr J Paediatr Surg 2020; 17 (1-2): 33-38
- 12 Łuczak J, Bagłaj M. Ovarian teratoma in children: a plea for collaborative clinical study. J Ovarian Res 2018; 11 (01) 75
- 13 Cowan RA, Haber EN, Faucz FR, Stratakis CA, Gomez-Lobo V. Mucinous cystadenoma in children and adolescents. J Pediatr Adolesc Gynecol 2017; 30 (04) 495-498
- 14 Azarakhsh N, Grimes S, Chotai PN, Shephard C, Huang EY. Post-resection outcomes for pediatric ovarian neoplasm: is ovarian-preserving surgery a good option?. Pediatr Surg Int 2017; 33 (01) 97-104
- 15 Abbas PI, Dietrich JE, Francis JA, Brandt ML, Cass DL, Lopez ME. Ovarian-sparing surgery in pediatric benign ovarian tumors. J Pediatr Adolesc Gynecol 2016; 29 (05) 506-510
- 16 Yousef Y, Pucci V, Emil S. The relationship between intraoperative rupture and recurrence of pediatric ovarian neoplasms: preliminary observations. J Pediatr Adolesc Gynecol 2016; 29 (02) 111-116
- 17 Rogers EM, Allen L, Kives S. The recurrence rate of ovarian dermoid cysts in pediatric and adolescent girls. J Pediatr Adolesc Gynecol 2014; 27 (04) 222-226
- 18 Hazard FK, Longacre TA. Ovarian surface epithelial neoplasms in the pediatric population: incidence, histologic subtype, and natural history. Am J Surg Pathol 2013; 37 (04) 548-553
- 19 Akkoyun I, Gülen S. Laparoscopic cystectomy for the treatment of benign ovarian cysts in children: an analysis of 21 cases. J Pediatr Adolesc Gynecol 2012; 25 (06) 364-366
- 20 Vaysse C, Delsol M, Carfagna L. et al. Ovarian germ cell tumors in children. Management, survival and ovarian prognosis. A report of 75 cases. J Pediatr Surg 2010; 45 (07) 1484-1490
- 21 Panteli C, Curry J, Kiely E. et al. Ovarian germ cell tumours: a 17-year study in a single unit. Eur J Pediatr Surg 2009; 19 (02) 96-100
- 22 Mann JR, Gray ES, Thornton C. et al; UK Children's Cancer Study Group Experience. Mature and immature extracranial teratomas in children: the UK Children's Cancer Study Group Experience. J Clin Oncol 2008; 26 (21) 3590-3597
- 23 De Backer A, Madern GC, Oosterhuis JW, Hakvoort-Cammel FG, Hazebroek FW. Ovarian germ cell tumors in children: a clinical study of 66 patients. Pediatr Blood Cancer 2006; 46 (04) 459-464
- 24 Cass DL, Hawkins E, Brandt ML. et al. Surgery for ovarian masses in infants, children, and adolescents: 102 consecutive patients treated in a 15-year period. J Pediatr Surg 2001; 36 (05) 693-699
- 25 Hermans AJ, Kluivers KB, Janssen LM. et al. Adnexal masses in children, adolescents and women of reproductive age in the Netherlands: a nationwide population-based cohort study. Gynecol Oncol 2016; 143 (01) 93-97
- 26 Caspi B, Appelman Z, Rabinerson D, Zalel Y, Tulandi T, Shoham Z. The growth pattern of ovarian dermoid cysts: a prospective study in premenopausal and postmenopausal women. Fertil Steril 1997; 68 (03) 501-505
- 27 Hoo WL, Yazbek J, Holland T, Mavrelos D, Tong EN, Jurkovic D. Expectant management of ultrasonically diagnosed ovarian dermoid cysts: is it possible to predict outcome?. Ultrasound Obstet Gynecol 2010; 36 (02) 235-240
- 28 Anteby EY, Ron M, Revel A, Shimonovitz S, Ariel I, Hurwitz A. Germ cell tumors of the ovary arising after dermoid cyst resection: a long-term follow-up study. Obstet Gynecol 1994; 83 (04) 605-608
- 29 Yasui T, Hayashi K, Mizunuma H. et al. Factors associated with premature ovarian failure, early menopause and earlier onset of menopause in Japanese women. Maturitas 2012; 72 (03) 249-255
- 30 Bjelland EK, Wilkosz P, Tanbo TG, Eskild A. Is unilateral oophorectomy associated with age at menopause? A population study (the HUNT2 Survey). Hum Reprod 2014; 29 (04) 835-841
- 31 Løkkegaard E, Jovanovic Z, Heitmann BL, Keiding N, Ottesen B, Pedersen AT. The association between early menopause and risk of ischaemic heart disease: influence of hormone therapy. Maturitas 2006; 53 (02) 226-233
- 32 Rocca WA, Bower JH, Maraganore DM. et al. Increased risk of cognitive impairment or dementia in women who underwent oophorectomy before menopause. Neurology 2007; 69 (11) 1074-1083
- 33 Zhu D, Chung HF, Dobson AJ. et al. Age at natural menopause and risk of incident cardiovascular disease: a pooled analysis of individual patient data. Lancet Public Health 2019; 4 (11) e553-e564