Allen C M, Camisa C, Hamzeh S, Stephens L
College of Dentistry, Section of Diagnostic Services, Ohio State University, Columbus.
J Am Acad Dermatol. 1990 Sep;23(3 Pt 1):444-50. doi: 10.1016/0190-9622(90)70238-d.
Six cases of cheilitis granulomatosa, a rare inflammatory disorder of unknown origin, are reported. The condition produces nontender, persistent swelling of one or both lips and affects primarily young adults. Histologically, nonnecrotizing granulomatous inflammation is seen. The clinical findings and results of therapy in these six cases are presented. One patient was treated with hydroxychloroquine sulfate (Plaquenil) that stabilized the process. One of our patients had vesicular-appearing lesions. Microscopic examination showed the lesions to be dilated superficial lymphatic channels, a finding that to our knowledge has not been previously described.
报告了6例肉芽肿性唇炎，这是一种病因不明的罕见炎症性疾病。该病表现为一侧或双侧唇部无痛性、持续性肿胀，主要累及年轻人。组织学检查可见非坏死性肉芽肿性炎症。本文介绍了这6例患者的临床 findings 和治疗结果。1例患者接受硫酸羟氯喹（羟氯喹）治疗后病情稳定。我们的1例患者有呈水疱样的 lesions。显微镜检查显示这些 lesions 为扩张的浅表淋巴管，据我们所知，这一发现此前尚未有过描述。
