Literature DB >> 8343057

Ovarian neoplasms in children.

M A Skinner1, M G Schlatter, S A Heifetz, J L Grosfeld.   

Abstract

OBJECTIVE: To review the clinical presentation, treatment, and outcome in a series of children with ovarian neoplasms.
DESIGN: A retrospective review of the medical records in a case series of 29 girls with ovarian neoplasms. The length of follow-up ranged from 6 months to 7 1/2 years and averaged 3.0 years in the girls with malignant tumors.
SETTING: The patients were treated at a large referral children's hospital. PATIENTS: Twenty-nine girls with ovarian neoplasms were treated from 1976 to 1992. The average age of the patients was 10 years and ranged from 2 to 16 years. MAIN OUTCOME MEASURES: The principal outcomes examined were mortality and surgical morbidity.
RESULTS: The most common presenting symptoms for these ovarian tumors in pediatric patients included chronic abdominal pain, an abdominal mass, or distention. Three girls presented with precocious puberty or hirsutism. In 27 cases, the tumor was a primary ovarian lesion. In two patients, the ovarian mass was the presenting finding for a stage IV non-Hodgkin's lymphoma. Seventeen tumors were benign and 12 were malignant. Tumors originating from the germ-cell line predominated (n = 17). Seven of the 10 ovarian malignant neoplasms were stage I at the time of diagnosis. All but one of the girls with malignant tumors received either adjunctive radiation therapy or multiple-agent chemotherapy. Two girls with sex cord/stromal cell tumors who presented with stage I disease ultimately developed widespread metastases. Both girls with large epithelial tumors survived. All of the girls with benign tumors and seven (70%) of 10 with malignant lesions survived.
CONCLUSION: Ovarian tumors are unusual lesions in the pediatric population. Unlike in adults, such neoplasms generally originate from the germ-cell line. Whereas most ovarian tumors in girls are benign, some children have malignant tumors that are very aggressive and do not respond well to adjuvant therapy. In particular, malignant sex cord/stromal cell tumors, even when they present at an early stage, may behave unpredictably.

Entities:  

Mesh:

Year:  1993        PMID: 8343057     DOI: 10.1001/archsurg.1993.01420200023004

Source DB:  PubMed          Journal:  Arch Surg        ISSN: 0004-0010


  13 in total

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2.  Post-resection outcomes for pediatric ovarian neoplasm: is ovarian-preserving surgery a good option?

Authors:  Nima Azarakhsh; Sandra Grimes; Pranit N Chotai; Claudette Shephard; Eunice Y Huang
Journal:  Pediatr Surg Int       Date:  2016-10-13       Impact factor: 1.827

Review 3.  Assessing gonadal function after childhood ovarian surgery.

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Review 4.  A pictorial review of imaging of abdominal tumours in adolescence.

Authors:  Darshana D Rasalkar; Winnie C W Chu; Frankie W T Cheng; Sze Ki Hui; Siu Cheung Ling; Chi Kong Li
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5.  Primary ovarian lymphoma in an infant: report of a case.

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6.  Ovarian mucinous borderline tumor with anaplastic carcinomatous nodules in adolescents.

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Review 7.  Ovarian neoplasms of childhood.

Authors:  Shailee V Lala; Naomi Strubel
Journal:  Pediatr Radiol       Date:  2019-10-16

8.  Clinicopathologic review of ovarian masses in Korean premenarchal girls.

Authors:  Eun Young Ki; Seung Won Byun; Yoon Jin Choi; Keun Ho Lee; Jong Sup Park; Sung Jong Lee; Soo Young Hur
Journal:  Int J Med Sci       Date:  2013-06-21       Impact factor: 3.738

Review 9.  Oxidative Stress during Ovarian Torsion in Pediatric and Adolescent Patients: Changing The Perspective of The Disease.

Authors:  Antonio Simone Laganà; Vincenza Sofo; Francesca Maria Salmeri; Vittorio Italo Palmara; Onofrio Triolo; Milan Milosav Terzić; Tito Silvio Patrelli; Adolf Lukanovic; Eda Vrtcnik Bokal; Giuseppe Santoro
Journal:  Int J Fertil Steril       Date:  2015-12-23

10.  A case report of a young girl with mucinous borderline tumor of the ovary.

Authors:  Hyun-Mi Lee; Kyeong A So; Mi Kyung Kim; Yoo Kyung Lee; In-Ho Lee; Tae-Jin Kim; Ki Heon Lee
Journal:  Obstet Gynecol Sci       Date:  2016-07-13
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