A comparative analysis of 57 serous borderline tumors with and without a noninvasive micropapillary component

被引:49
作者
Slomovitz, BM
Caputo, TA
Gretz, HF
Economos, K
Tortoriello, DV
Schlosshauer, PW
Baergen, RN
Isacson, C
Soslow, RA
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, New York Presbyterian Hosp, Dept Obstet & Gynecol, New York, NY USA
[3] Cornell Univ, Weill Med Coll, New York Presbyterian Hosp, Div Gynecol Oncol, New York, NY USA
[4] Cornell Univ, Weill Med Coll, New York Presbyterian Hosp, Dept Pathol, New York, NY USA
[5] Mt Sinai Sch Med, Dept Obstet & Gynecol, Div Gynecol Oncol, New York, NY USA
[6] Mt Sinai Sch Med, Dept Pathol, New York, NY USA
[7] New York Methodist Hosp, Div Gynecol Oncol, Dept Obstet & Gynecol, Brooklyn, NY USA
[8] Brigham & Womens Hosp, Div Reprod Endocrinol & Infertil, Dept Obstet & Gynecol, Boston, MA 02115 USA
[9] Virginia Mason Med Ctr, Dept Pathol, Seattle, WA 98101 USA
[10] Cornell Univ, Weill Med Coll, New York, NY USA
关键词
serous borderline tumor; low malignant potential; micropapillary serous carcinoma; noninvasive implant; invasive implant;
D O I
10.1097/00000478-200205000-00005
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The literature concerning serous borderline tumors With a non-invasive micropapillary component suggests an association with invasive implants. We compared the clinicopathologic features of micropapillary serous borderline tumors (MSBTs) with typical SBTs to determine the following: 1) the importance of focal micropapillary architecture in an otherwise typical SBT, 2) the behavior of low-stage MSBTs, 3) Whether high-stage MSBTs are inherently more aggressive than high-stage SBTs, and 4) Whether invasive implants are prevalent in an MSBT cohort without referral selection bias. The 57 borderline tumors studied were diagnosed at a university hospital between 1981 and 1998; they included 14 MSBTs, 35 SBTs, and 8 SBTs with focal micropapillary features. None of the specimens were referrals for expert pathologic consultation, thus distinguishing our study group from most of those previously reported, Neither MSBTs nor SBTs were associated With invasive implants at diagnosis (0 of 14 and 0 of 43, respectively). They also did not differ With respect to overall stage at diagnosis, but MSBTs were more frequently bilateral than SBTs (71% versus 23%, p = 0.001). There was an increased risk of recurrence in MSBT versus SBT (3 of 14 versus 1 of 43, p = 0.035), but this was stage related; there was no difference between groups when evaluating recurrence in stage 1 disease (0 of 8 versus 0 of 27). There was no difference in recurrence or stage at diagnosis between SBTs with focal micropapillary features and other SBTs. There was 100% survival in all groups. We conclude that high-stage MSBTs With noninvasive implants should be considered a subtype of SBTs with an increased risk of recurrence. Stage 1 MSBTs demonstrate clinical features that are similar to low-stage SBTs. Focal micropapillary architecture (<5 mm) has no bearing on outcome. MSBTs in the general population are not strongly associated with invasive implants.
引用
收藏
页码:592 / 600
页数:9
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