Original articleCheilitis glandularis: A clinicopathological study in 22 patients
Section snippets
Objectives
Clinicopathological findings of 22 patients with CG from the oral diseases clinic at the dermatology department at our university are presented. Therapies used were reviewed along with histopathological aspects, with emphasis at the possible presence of SCC.
Methods
Records of 22 patients with clinical diagnosis of CG were reviewed. General data such as sex, age, and race were studied. Description of clinical lesions and associated significant dermatologic diseases were considered, as were therapies used and histopathological aspects. When surgery was performed, it consisted of a lower lip vermilionectomy followed by careful dissection and removal of minor mucous salivary glands associated. The surgical fragments were formalin fixed and the vermilion was
Results
A summary of the findings is shown in Table I. In all, 22 patients were given the diagnosis of CG, with a male preponderance (17 male, 5 female). Patient age varied from 20 to 69 years. Most patients were white and photosensitive; there were 6 albino patients (all nonwhite patients were albinos). CG was present on the lower lip of all patients and in the upper lip of 6 patients. The clinical picture varied from mild infiltration of the lip with visible ostia draining a discrete amount of
Discussion
The cause of CG is unknown. It was once considered a primary disease of minor salivary glands (heterotopia X hyperplasia),3 but Swerlick and Cooper2 compared histologic material from patients with CG with that of control subjects and found no differences in size, depth, or appearance of minor salivary glands. These authors suggest that CG represents a reaction pattern in response to chronic irritation of the lips (actinic, atopic, or factitious) and is unrelated to gland hyperplasia or
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2021, Journal of Oral and Maxillofacial Surgery, Medicine, and PathologyCitation Excerpt :When there is associated fungal infection, antifungal agents should be used [2,16–20,23]. Cheilitis glandularis (CG) is a rare inflammatory condition of uncertain origin, which affects the lower salivary glands of the lip of predominantly male and fair-skinned individuals [3,24,25]. Some authors consider that this disease has endogenous origin in altered small salivary glands located in the labial mucosa.
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Funding sources: None.
Conflicts of interest: None declared.