Quispel R, van Boxel O S, Schipper M E, Sigurdsson V, Canninga-van Dijk M R, Kerckhoffs A, Smout A J, Samsom M, Schwartz M P
Department of Gastroenterology, University Medical Center Utrecht, Utrecht, The Netherlands.
Endoscopy. 2009 Mar;41(3):187-93. doi: 10.1055/s-0028-1119590. Epub 2009 Mar 11.
The first cases of squamous cell carcinoma in esophageal lichen planus were recently described. We performed a study to establish the prevalence of endoscopic and histopathologic abnormalities consistent with lichen planus and (pre-) malignancy in a cohort of patients with lichen planus.
A total of 24 patients with lichen planus were prospectively studied using high-magnification chromoendoscopy. Focal esophageal abnormalities were mapped, classified, and biopsied. Biopsies were also taken from normal-appearing esophageal mucosa at three levels (proximal, middle, and distal). The presence of a lymphohistiocytic interface inflammatory infiltrate and Civatte bodies (i. e. apoptotic basal keratinocytes) at histopathologic examination was considered diagnostic for esophageal lichen planus. Symptoms were assessed using validated questionnaires.
A total of 38 focal abnormalities were biopsied. These consisted of: layers of mucosa peeling off, hyperemic lesions, papular lesions, submucosal plaques/papules, a flat polypoid lesion, and segments of cylindrical epithelium. No endoscopic signs of dysplasia were present. Esophagitis consistent with gastroesophageal reflux disease was noted in 12 / 24 patients. Histopathology showed chronic inflammation of the esophageal mucosa in the majority (18 / 24) of patients. In 50 % (12 / 24), the diagnosis of esophageal lichen planus was made. Dysplasia was not present. There were no differences in symptoms between patients with and without esophageal lichen planus.
At screening endoscopy a high prevalence (50 %) of esophageal lichen planus was found in patients with orocutaneous lichen planus. No dysplasia was found.
最近报道了首例食管扁平苔藓伴鳞状细胞癌的病例。我们开展了一项研究,以确定一组扁平苔藓患者中与扁平苔藓及(癌前)恶性病变相符的内镜和组织病理学异常的患病率。
对24例扁平苔藓患者进行前瞻性高倍放大色素内镜检查。对局部食管异常进行定位、分类并活检。还从食管近端、中段和远端三个层面外观正常的食管黏膜取材活检。组织病理学检查中存在淋巴细胞-组织细胞界面炎性浸润和基底层凋亡角质形成细胞(即Civatte小体)被视为食管扁平苔藓的诊断依据。使用经过验证的问卷评估症状。
共对38处局部异常进行了活检。这些异常包括:黏膜层剥脱、充血性病变、丘疹样病变、黏膜下斑块/丘疹、扁平息肉样病变以及柱状上皮段。未发现发育异常的内镜征象。24例患者中有12例存在与胃食管反流病相符的食管炎。组织病理学显示大多数患者(24例中的18例)食管黏膜有慢性炎症。50%(24例中的12例)患者被诊断为食管扁平苔藓。未发现发育异常。有食管扁平苔藓和无食管扁平苔藓的患者在症状方面无差异。
在筛查内镜检查中,发现口腔皮肤扁平苔藓患者中食管扁平苔藓的患病率较高(50%)。未发现发育异常。