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Springtime papules, plaques, and cheilitis. Polymorphous light eruption (PMLE)
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Successful treatment of granulomatous cheilitis with thalidomide.
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Cheilitis glandularis; a manifestation of emotional disturbance.
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Cheilitis granulomatosa and Melkersson-Rosenthal syndrome.
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Persistent swelling of the lower lip. Cheilitis granulomatosa.
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Cheilitis caused by cinnamon (Cassia) oil in tooth paste.
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[Relation of the Melkersson-Rosenthal syndrome to Miescher's cheilitis granulomatosis].
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[Persistent hemorrhagic crusts on the lips of a 13-year-old patient. Cheilitis crustosa factitia].
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[CO2 laser vaporization in cheilitis actinica. Current comment on the contribution by S. Hohenleutner, M. Landthaler and U. Hohenleutner].
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Cheilitis granulomatosa. Report of case treated with injection of triamcinolone acetonide aqueous suspension.
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Idiopathic gingivostomatitis. Cheilitis, glossitis, gingivitis syndrome; atypical gingivostomatitis, plasma-cell gingivitis, plasmacytosis of gingiva.
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Cheilitis granulomatosa (Melkersson-Rosenthal syndrome).
An oligosymptomatic manifestation of the Melkersson-Rosenthal syndrome is described. The importance of serial sections of the tissue specimen is emphasized. Satisfactory postoperative results are obtained.
Histopathology and electron and immunofluorescence microscopy of gingivitis granulomatosa associated with glossitis and cheilitis in a case of Anderson-Fabry disease.
A 17-year-old white boy with signs, symptoms, and family history of angiokeratoma corporis diffusum universale, Anderson-Fabry disease (AFD), developed recurrent and then persistent swelling of both lips, erythematous hyperplastic gingivae, and a pebbled tongue. Positive blood findings were raised serum IgE, decreased T-cell level, and increased B-cell level. Histopathology of the gingiva showed noncaseating granulomas with multinucleate giant cells containing Schaumann bodies and large plasma-cell infiltrates in which immunofluorescence demonstrated immune globulins of several classes. Electron microscopy and histochemistry demonstrated ceramide in the vasculature. No glycolipid was found in the macrophages or giant cells of the granulomas which, in contrast, resembled sarcoid reactions. Plasma cells with Russell bodies and immune reaction-induced degranulation of mast cells were also identified. The pathogenesis of the oral findings possibly relates to altered immune reactivity associated with damage to the microvasculature analogous to that in Melkersson-Rosenthal syndrome.