Leiomyomatosis peritonealis disseminata with aromatase cytochrome P450 expression in a postmenopausal woman: a case study with literature review

被引:0
|
作者
Matsuya, M. O. [1 ]
Sugihara, K. [1 ]
Yaguchi, C. [1 ]
Itoh, H. [1 ]
Kitamura, H. [3 ]
Kanayama, N. [1 ]
Arahori, K. [2 ]
机构
[1] Hamamatsu Univ Sch Med, Obstet & Gynaecol, Higashi Ku, Hamamatsu, Shizuoka, Japan
[2] Ito Municipal Hosp, Obstet & Gynaecol, Ito, Shizuoka, Japan
[3] Ito Municipal Hosp, Pathol, Ito, Shizuoka, Japan
关键词
Leiomyomatosis peritonealis disseminata; Postmenopause; Malignant; Estradiol; Aromatase immunostaining; MALIGNANT CHANGE; HORMONE AGONIST; ESTROGEN; CELLS;
D O I
10.12892/ejgo4120.2018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of Investigation: The authors aimed to assess the hypothesis that leiomyomatosis peritonealis disseminata (LPD) in a postmenopausal woman had autocrine estrogen secretion abilities. Materials and Methods: A 73-year-old woman presented with a bulky tumour in the peritoneal cavity. The pathological diagnosis was LPD or sarcoma of unknown origin. Medroxyprogesterone acetate (MPA) and GnRH analogue therapies were effective, but a tumour mass was confirmed with rapid growth immediately after the cessation of treatment and led to her death from intra-tumour haemorrhage. The authors evaluated the mechanism of tumour using immunostaining for aromatase cytochrome P450. Results: The tumour showed high expression of aromatase. The immunostaining patterns of estrogen receptor (ER), progesterone receptor (PgR), and aromatase were similar to those of a premenopausal leiomyoma. Conclusion: It is likely that the tumour had the autocrine ability to secrete estrogen and that tumour growth resumed because of a flare-up caused by the downregulation of hormonal therapies.
引用
收藏
页码:838 / 842
页数:5
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