Department of Oral and Maxillofacial Diagnostic Sciences, University of Florida College of Dentistry, Gainesville, FL, USA.
J Oral Pathol Med. 2019 Oct;48(9):846-854. doi: 10.1111/jop.12918. Epub 2019 Jul 4.
Lichenoid granulomatous reaction can be subcategorized into lichenoid granulomatous dermatitis or lichenoid granulomatous stomatitis. It is described in the literature as demonstrating a band-like lichenoid infiltration with clusters of histiocytic or granuloma formation. In this study, we presented a large case series of lichenoid granulomatous stomatitis including demographics, histological features, and subcategories and compared findings with current literature.
We retrieved all cases diagnosed with lichenoid reaction with granulomatous inflammation between January 1, 2000, and August 1, 2016, from the University of Florida Oral Pathology Biopsy Service Archives.
A total of 47 patients with tissue from 50 biopsy sites were included. The majority of the cases were noted in females (64%) with a mean age of 59 years (range 30-88). Most patients were Caucasian, and the most common sites in descending order were: gingiva, buccal mucosa, vestibule, tongue, lip, palate, and occasional multifocal involvement. Clinical impressions by the treating clinicians included leukoplakia, dysplasia, carcinoma in situ, squamous cell carcinoma, lichen planus, vesiculobullous disease, trauma, and allergy. The histologic features of these cases ranged from lichenoid mucositis with numerous aggregates of histiocytes to well-formed granulomas, in accordance with previous classifications of similar dermatologic lesions. All cases revealed positive CD 68 in the histiocytic infiltrates and were negative for microorganisms utilizing acid-fast bacilli, Grocott methenamine-silver, and periodic acid-Schiff stains.
Lichenoid granulomatous disease may be more common than previously reported; however, its etiology remains unknown and patients should be kept under long-term clinical follow-up.
苔藓样肉芽肿反应可分为苔藓样肉芽肿性皮炎或苔藓样肉芽肿性口炎。文献中描述其表现为具有带状苔藓样浸润,伴有组织细胞或肉芽肿形成簇。在本研究中,我们报告了一系列大型苔藓样肉芽肿性口炎病例,包括人口统计学、组织学特征和亚型,并与当前文献进行了比较。
我们从佛罗里达大学口腔病理学活检服务档案中检索了 2000 年 1 月 1 日至 2016 年 8 月 1 日期间诊断为苔藓样反应伴肉芽肿性炎症的所有病例。
共纳入 47 例患者,共 50 个活检部位。大多数病例为女性(64%),平均年龄为 59 岁(范围 30-88 岁)。大多数患者为白种人,最常见的部位依次为:牙龈、颊黏膜、前庭、舌、唇、腭,偶尔也有多灶性受累。治疗医生的临床印象包括:白斑、发育不良、原位癌、鳞状细胞癌、扁平苔藓、水疱性大疱病、创伤和过敏。这些病例的组织学特征从具有大量组织细胞聚集的苔藓样黏膜炎到形成良好的肉芽肿不等,符合先前类似皮肤病损的分类。所有病例的组织细胞浸润均显示 CD68 阳性,利用抗酸杆菌、Grocott 六胺银和过碘酸-Schiff 染色均为微生物阴性。
苔藓样肉芽肿性疾病可能比先前报道的更为常见;然而,其病因仍不清楚,患者应长期进行临床随访。