Department of Oral Diagnostic Services, Howard University College of Dentistry (ELBC), Howard University College of Dentistry, Washington, DC 20059, USA.
Ann Diagn Pathol. 2011 Jun;15(3):157-61. doi: 10.1016/j.anndiagpath.2010.10.003. Epub 2011 Mar 10.
Congenital epulis of the newborn (CEN) is a rare benign lesion that exclusively occurs in the oral and maxillofacial regions of newborns. The clinicopathologic features of CEN were examined and reviewed from the files of the Armed Forces Institute of Pathology from 1970 to 2000. Ten cases were included. Patient lesions were all present at birth but were surgically excised between 2 days and 6 weeks (median, 5.5 days). Nine lesions were in females; 1 case did not designate patient sex. Locations included 6 on the maxilla, 2 on the mandible, 1 on the designated maxillary lip, and 1 unknown. The cases included a patient with 2 lesions: 1 on mandibular and 1 on maxillary alveolar ridges, respectively. All other lesions were solitary and polypoid. Microscopically, these were pedunculated and nodular, composed of sheets to grouped clusters of medium-sized, ovoid-to-polygonal cells with abundant granular cytoplasm, distinct cell membranes, vascular-rich stroma, and attenuated overlying mucosa. Two cases also demonstrated spindled cells. The nuclei were vesicular and focally stippled, with distinct and slightly convoluted nuclear membranes; nucleoli were visible but not prominent. Mitotic activity was not observed. The vascular channels ranged from capillary-sized to venous, some staghorn-like with rare perivascular long-term inflammation. The venules exhibited a perivascular pericytic proliferation. Odontogenic epithelial rests were present in 2 cases. No cases demonstrated cytoplasmic hyaline globules. The lesional cells in all cases were negative for S-100 protein, CD68, CD34, CD31, keratins, desmin, calponin, and smooth muscle actin. Perivenular pericytes were positive for smooth muscle actin. Congenital epulis of the newborn is a rare oral entity with characteristic clinicopathologic features. It predominately affects girls, mainly on the maxillary alveolar ridge. It may be separated from "granular cell tumor" by location, patient age, absence of cytoplasmic hyaline globules, solid growth pattern, pericytic proliferation, attenuated overlying epithelium, and negativity for S-100 protein.
新生儿先天性龈瘤(CEN)是一种罕见的良性病变,仅发生于新生儿的口腔和颌面部。本研究从 1970 年至 2000 年武装部队病理研究所的档案中检查和回顾了 CEN 的临床病理特征。共纳入 10 例患者。病变均于出生时出现,但在出生后 2 天至 6 周(中位数 5.5 天)间被手术切除。9 例病变位于女性;1 例未指明患者性别。病变位置包括上颌 6 例、下颌 2 例、上颌唇 1 例、上颌牙槽嵴 1 例。此外,1 例患者存在 2 处病变:1 处位于下颌、1 处位于上颌牙槽嵴。所有其他病变均为单发息肉样。镜下,这些病变呈有蒂和结节状,由中到大的、卵圆形至多边形细胞组成,细胞排列成片状或成簇状,细胞浆丰富呈颗粒状,细胞膜清晰,富含血管的间质,以及萎缩的覆盖黏膜。2 例还显示梭形细胞。细胞核呈泡状,局灶性点彩状,核膜清晰且略卷曲;核仁可见但不明显。未见有丝分裂活性。血管大小从毛细血管到静脉不等,有些呈鹿角状,伴罕见的血管周围慢性炎症。小静脉表现为血管周周细胞增生。2 例可见牙源性上皮剩余。无病例显示细胞质透明小体。所有病例的病变细胞 S-100 蛋白、CD68、CD34、CD31、角蛋白、结蛋白、钙调蛋白和平滑肌肌动蛋白均为阴性。血管周周细胞阳性表达平滑肌肌动蛋白。新生儿先天性龈瘤是一种罕见的口腔实体瘤,具有特征性的临床病理特征。它主要影响女性,主要位于上颌牙槽嵴。它可以通过位置、患者年龄、无细胞质透明小体、实性生长方式、周细胞增生、萎缩的覆盖上皮以及 S-100 蛋白阴性与“颗粒细胞瘤”相区分。