Longacre T A, Fenoglio-Preiser C M
VA Medical Center, Albuquerque, New Mexico.
Am J Surg Pathol. 1990 Jun;14(6):524-37. doi: 10.1097/00000478-199006000-00003.
We present the clinicopathologic characteristics of 110 colorectal mixed hyperplastic adenomatous polyps (MHAP) that exhibited the architectural but not the cytologic features of a hyperplastic polyp. They are compared with 60 traditional adenomas, 40 hyperplastic polyps, and five colonic polyps that contained admixed but well-defined hyperplastic and adenomatous glands (HP/AD). The patients with MHAP ranged in age from 15 to 88 years (mean, 63 years). Five patients had two or more (up to seven) lesions. MHAP measured 0.2-7.5 cm in diameter. They were distributed throughout the colorectum, but a slight preponderance of large lesions (more than 1.0 cm) occurred in the cecum and appendix. All MHAP were characterized by a serrated glandular pattern simulating that seen in hyperplasia (27% of MHAP were initially diagnosed as hyperplastic polyps). However, MHAP were distinguished by the presence of goblet cell immaturity, upper zone mitoses, prominence of nucleoli, and the absence of a thickened collagen table. Although surface mitotic activity, nuclear pseudostratification, and nuclear cytoplasmic ratio were greater in MHAP than in hyperplastic polyps, they were slightly less than in traditional adenomas. Thirty-seven percent of MHAP contained foci of significant dysplasia; 11% contained areas of intramucosal carcinoma. We conclude that these lesions reflect a morphologically unique variant of adenoma and suggest that they be termed "serrated adenoma" in order to emphasize their neoplastic nature. We further offer the hypothesis that MHAP may arise from the neoplastic transformation of a more differentiated cell in the crypt than the traditional adenoma.
我们呈现了110例结直肠混合增生性腺瘤性息肉(MHAP)的临床病理特征,这些息肉呈现出增生性息肉的结构特征,但不具备其细胞学特征。将它们与60例传统腺瘤、40例增生性息肉以及5例含有混合但界限分明的增生性和腺瘤性腺体的结肠息肉(HP/AD)进行比较。MHAP患者年龄在15至88岁之间(平均63岁)。5例患者有两个或更多(最多7个)病变。MHAP直径为0.2 - 7.5厘米。它们分布于整个结直肠,但盲肠和阑尾中稍多一些大病变(超过1.0厘米)。所有MHAP均以锯齿状腺管模式为特征,类似增生所见(27%的MHAP最初被诊断为增生性息肉)。然而,MHAP的特征在于存在杯状细胞不成熟、上皮区有丝分裂、核仁突出以及缺乏增厚的胶原板。尽管MHAP的表面有丝分裂活性、核假复层化和核质比高于增生性息肉,但略低于传统腺瘤。37%的MHAP含有显著发育异常灶;11%含有黏膜内癌区域。我们得出结论,这些病变反映了腺瘤的一种形态学独特变体,并建议将它们称为“锯齿状腺瘤”,以强调其肿瘤性质。我们进一步提出假说,即MHAP可能起源于隐窝中比传统腺瘤更分化的细胞的肿瘤性转化。