Sankar Roshna, Tomar Arushi, John Sharon, Verma Veerendra, Gupta Shalini
Department of Oral & Maxillofacial Pathology and Oral Microbiology, King George's Medical University, Lucknow, India.
Department of ENT, King George's Medical University, Lucknow, 226003 India.
Indian J Otolaryngol Head Neck Surg. 2024 Aug;76(4):3519-3523. doi: 10.1007/s12070-024-04593-z. Epub 2024 Mar 18.
The term "idiopathic lymphoplasmacellular mucositis" (ILPM) refers to a set of conditions marked by extensive lymphocyte and plasma cell infiltrates in the submucosa which can involve the oral cavity, upper respiratory tract and the genital epithelium. There is no recognized cause of ILPM, and the diagnosis is mostly done on an exclusion basis. Herein, we report a 32-year-old man presented with an erosive ulcerated lesion on the hard palate and review the literature regarding the possible differential diagnosis including squamous cell carcinoma. We also reviewed the previously reported cases of ILPM with palatal involvement to summarise clinical presentation, treatment, and outcome of the entity to date.
术语“特发性淋巴浆细胞性黏膜炎”（ILPM）指的是一组以黏膜下层广泛淋巴细胞和浆细胞浸润为特征的病症，可累及口腔、上呼吸道和生殖上皮。ILPM的病因尚不明确，诊断主要基于排除法。在此，我们报告一名32岁男性，其硬腭出现糜烂性溃疡性病变，并回顾了包括鳞状细胞癌在内的可能鉴别诊断的文献。我们还回顾了先前报道的腭部受累的ILPM病例，以总结该疾病目前的临床表现、治疗方法及预后情况。
