Serial histologic observation of endometrial adenocarcinoma treated with high-dose progestin until complete disappearance of carcinomatous foci-review of more than 25 biopsies from five patients

被引:11
作者
Kamoi, S. [1 ]
Ohaki, Y. [2 ]
Mori, O. [2 ]
Kurose, K. [3 ]
Fukunaga, M. [4 ]
Takeshita, T. [3 ]
机构
[1] Chiba Hokusoh Hosp, Nippon Med Sch, Dept Obstet & Gynecol, Chiba, Japan
[2] Chiba Hokusoh Hosp, Nippon Med Sch, Dept Surg Pathol, Chiba, Japan
[3] Nippon Med Sch, Dept Obstet & Gynecol, Tokyo 113, Japan
[4] Jikei Univ, Daisan Hosp, Dept Pathol, Tokyo, Japan
关键词
high-dose progestin therapy; histologic changes of endometrial adenocarcinoma; medroxyprogesterone acetate (MPA);
D O I
10.1111/j.1525-1438.2007.01166.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Kamoi S, Ohaki Y, Mori O, Kurose K, Fukunaga M, Takeshita T. Serial histologic observation of endometrial adenocarcinoma treated with high-dose progestin until complete disappearance of carcinomatous foci-review of more than 25 biopsies from five patients. Int J Gynecol Cancer 2008;18:1305-1314. This study aimed to document chronologic histologic changes of endometrial biopsies from patients with endometrial adenocarcinoma on high-dose progestin therapy. Seven patients with presumptive FIGO stage IA endometrial adenocarcinoma treated with medroxyprogesterone acetate 600 mg/day were investigated retrospectively. Good response was defined as complete disappearance of carcinoma foci within 16 weeks of treatment and poor response as the presence of residual foci at 16 weeks. Two patients were poor responders and were excluded from the study, while five good responders were analyzed. Hematoxylin and eosin (H&E)-stained slides were reviewed and analyzed based on nine histologic features to describe the histology observed commonly in good responders. All the five good responders showed relatively uniform morphologic changes during the high-dose progestin therapy and the common histology was described as follows. The first change was swelling of the neoplastic glandular epithelial cells with pale vacuolated cytoplasm and round to oval nuclei. Mitotic arrest was also observed. Next, the epithelia were disrupted by lymphoplasmocytic infiltration and replaced by low cuboidal epithelium with or without squamous or morular metaplasia. The stromal area increased with predecidual changes. The final morphology was small atrophic glands scattered in predecidual stroma with dilated vessels. Therefore, the morphologic change of the endometrial biopsy observed in earlier stage of treatment might be able to predict good response to high-dose progestin therapy.
引用
收藏
页码:1305 / 1314
页数:10
相关论文
共 31 条
[1]   Apoptosis may be an early event of progestin therapy for endometrial hyperplasia [J].
Amezcua, CA ;
Lu, JJ ;
Felix, JC ;
Stanczyk, FZ ;
Zheng, WX .
GYNECOLOGIC ONCOLOGY, 2000, 79 (02) :169-176
[3]  
BUCKLEY CH, 2002, BIOPSY PATHOLOGY END, P56
[4]   Intratumoral effects of medroxy-progesterone on proliferation, apoptosis, and sex steroid receptors in endometrioid endometrial adenocarcinoma [J].
Dahmoun, M ;
Boman, K ;
Cajander, S ;
Bäckström, T .
GYNECOLOGIC ONCOLOGY, 2004, 92 (01) :116-126
[5]  
DELIGDISCH L, 1993, MODERN PATHOL, V6, P94
[6]   Classification and grading of gastritis - The updated Sydney System [J].
Dixon, MF ;
Genta, RM ;
Yardley, JH ;
Correa, P ;
Batts, KP ;
Dahms, BB ;
Filipe, MI ;
Haggitt, RC ;
Haot, J ;
Hui, PK ;
Lechago, J ;
Lewin, K ;
Offerhaus, JA ;
Price, AB ;
Riddell, RH ;
Sipponen, P ;
Solcia, E ;
Watanabe, H .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1996, 20 (10) :1161-1181
[7]  
DUSKA LR, 2004, UTERINE CANC, P144
[8]   Progression of conservatively treated endometrial carcinoma after full term pregnancy: A case report [J].
Ferrandina, G ;
Zannoni, GF ;
Gallotta, V ;
Foti, E ;
Mancuso, S ;
Scambia, G .
GYNECOLOGIC ONCOLOGY, 2005, 99 (01) :215-217
[9]   Unsuspected uterine carcinosarcoma (heterologous) diagnosed following conservative therapies with medroxyprogesterone acetate for presumed early-stage endometrial carcinoma [J].
Fujiwara, H ;
Shibahara, H ;
Usui, R ;
Takamizawa, S ;
Kosuge, S ;
Ohwada, M ;
Suzuki, M ;
Sato, I .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2002, 47 (03) :129-131
[10]  
Jobo T, 2000, EUR J GYNAECOL ONCOL, V21, P119