Adolescent ovarian thecoma presenting as progressive hyperandrogenism: case report and review of the literature

被引:4
作者
Gaspari, Laura [1 ,2 ]
Paris, Francoise [1 ,2 ]
Taourel, Patrice [2 ,3 ]
Soyer-Gobillard, Marie-Odile [4 ]
Kalfa, Nicolas [2 ,5 ]
Sultan, Charles [1 ,2 ]
机构
[1] CHU Montpellier, Dept Pediat, Unite Endocrinol Gynecol Pediat, Hop A de Villeneuve, F-34295 Montpellier 5, France
[2] Univ Montpellier, Montpellier, France
[3] CHU Montpellier, Dept Imagerie, Hop Lapeyronie, Montpellier, France
[4] Sorbonne Univ, Assoc Hhorages France, CNRS, F Asnieres Sur Oise, France
[5] CHU Montpellier, Dept Chirurg Pediat, Hop Lapeyronie, Montpellier, France
关键词
Adolescent hyperandrogenism; hirsutism; ovarian thecoma; endocrine disruptor chemicals; SCLEROSING PERITONITIS; LUTEINIZED THECOMAS; FIBROMA; EXPOSURE; TUMORS; RECURRENT; CHILDREN; GENE;
D O I
10.1080/09513590.2020.1739265
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hyperandrogenism is frequent and under investigated in adolescent girls. A 15-year-6-month-old French girl presented with oligomenorrhea and slowly progressing virilization 2 years post-menarche. Medical history revealed prenatal pesticide exposure through maternal professional activity and recurrent premature thelarche. Severe hirsutism, mild facial acne and clitoromegaly were noted. Serum androgens (testosterone: 94 ng/dL, 4-androstenedione: 8.23 ng/mL) were high and non-classic 21-hydroxylase deficiency was excluded. Pelvic ultrasonography showed a left ovarian mass, confirmed by computed tomography scan. Tumor markers were negative. Laparoscopic surgery was performed. The pathological diagnosis was benign luteinized thecoma. Postoperatively, the menstrual cycle and serum androgens became normal and hirsutism slowly improved. Hyperandrogenism 2 years after menarche should be systematically investigated, even if slowly progressive, since it may be a symptom of a rare virilizing ovarian tumor, like thecoma.
引用
收藏
页码:839 / 842
页数:4
相关论文
共 39 条
[1]  
AMIN HK, 1971, CANCER, V27, P438, DOI 10.1002/1097-0142(197102)27:2<438::AID-CNCR2820270231>3.0.CO
[2]  
2-4
[3]   BILATERAL OVARIAN FIBROMAS IN A 5-YEAR-OLD [J].
BOWER, JF ;
ERICKSON, ER .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1967, 99 (06) :880-&
[4]   Thecoma of the Ovary A Report of 70 Cases Emphasizing Aspects of Its Histopathology Different From Those Often Portrayed and Its Differential Diagnosis [J].
Burandt, Eike ;
Young, Robert H. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2014, 38 (08) :1023-1032
[5]   A large abdominal mass in a young girl [J].
Chan, CY ;
Chan, SM ;
Liauw, L .
BRITISH JOURNAL OF RADIOLOGY, 2000, 73 (872) :913-914
[6]   OVARIAN TUMORS IN CHILDHOOD - REPORT OF 6 NEW CASES AND REVIEW OF THE LITERATURE [J].
CHARACHE, H .
ARCHIVES OF SURGERY, 1959, 79 (04) :573-580
[7]   Ovarian thecoma-fibroma groups: clinical and sonographic features with pathological comparison [J].
Chen, Hui ;
Liu, Yan ;
Shen, Li-fei ;
Jiang, Mei-jiao ;
Yang, Zhi-fang ;
Fang, Guo-ping .
JOURNAL OF OVARIAN RESEARCH, 2016, 9 :1-7
[8]   Ovarian fibroma in a 7-month-old infant: a case report and review of the literature [J].
Chen, YJ ;
Hsieh, CS ;
Eng, HL ;
Huang, CC .
PEDIATRIC SURGERY INTERNATIONAL, 2004, 20 (11-12) :894-897
[9]   SCLEROSING PERITONITIS ASSOCIATED WITH LUTEINIZED THECOMAS OF THE OVARY - A CLINICOPATHOLOGICAL ANALYSIS OF 6 CASES [J].
CLEMENT, PB ;
YOUNG, RH ;
HANNA, W ;
SCULLY, RE .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1994, 18 (01) :1-13
[10]  
Dhull A, 2013, INT J 3 WORLD MED, V9, p105580/16c2, DOI DOI 10.5580/16C2