Mesonephric-like adenocarcinomas of the uterine corpus: report of a case series and review of the literature indicating poor prognosis for this subtype of endometrial adenocarcinoma

被引:60
作者
Horn, Lars-Christian [1 ]
Hoehn, Anne Kathrin [1 ]
Kruecken, Irene [2 ]
Stiller, Mathias [2 ]
Obeck, Ulrike [2 ]
Brambs, Christine E. [3 ]
机构
[1] Univ Hosp Leipzig, Div Gynecol Breast & Perinatal Pathol, Inst Pathol, Liebigstr 26, D-04103 Leipzig, Germany
[2] Univ Hosp Leipzig, Inst Pathol, Div Mol Pathol, Leipzig, Germany
[3] Tech Univ Munich, Dept Obstet & Gynecol, Munich, Germany
关键词
Endometrium; Cancer; Mesonephric; Adenocarcinoma; TTF-1; Prognosis; KRAS-mutation; PD-L1; INTERNATIONAL SOCIETY; CARCINOMA; RECOMMENDATIONS; MUTATIONS; CERVIX;
D O I
10.1007/s00432-019-03123-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Endometrial mesonephric-like adenocarcinoma (ML-AC) represents a recently recognized subtype of endometrial adenocarcinoma (AC) associated with a subtle immunophenotype with a characteristic KRAS-mutation. Detailed clinico-pathologic analyses and prognostic data on ML-AC are limited. Methods We report a series of four cases with histopathological, immunohistochemical, and molecular analyses. These cases as well as the data of previously published cases were reviewed for clinico-pathologic variables and clinical follow-up information. Results Forty cases of ML-AC were identified. ML-AC represents about 1% of all endometrial carcinomas. Similar to other types of endometrial AC, vaginal bleeding was the leading presenting symptom, and the mean age was 60.0 years (range 31-91). More than a half of the patients presented with locally advanced disease (>= FIGO stage II) at time of diagnosis, developed a recurrence or died of the disease within a mean follow-up period of 24.7 months (range 3-144.5 months). The most common site of distant disease was pulmonary involvement. Microscopically, ML-ACs present with mixed morphology and show a co-expression of so-called mesonephric and Mullerian markers, suggesting a Mullerian origin of the tumors. Immunostaining for PD-L1 was negative in all tested cases, using different antibodies against PD-L1. Retained staining for mismatch repair proteins on immunohistochemistry and a POLE-mutation suggest a copy number low phenotype within the molecular classification of endometrial carcinomas. Almost all cases showed a KRAS-mutation at codon 12 (mostly G12V). Conclusion Uterine ML-AC represents a distinct subtype of invasive endometrial AC, associated with KRAS-mutations and characteristic immunohistochemical findings. Clinically, ML-AC may show an aggressive behavior with a high rate of recurrent disease and a substantial risk for distant metastatic disease, especially to the lungs.
引用
收藏
页码:971 / 983
页数:13
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