Results 21 to 30 of about 11,670 (169)

Cheilitis granulomatosa.

open access: yesJ Oral Maxillofac Pathol, 2013
Kavya B, Gite M, Bhat M, Paremala K.
europepmc   +5 more sources

Miescher's cheilitis granulomatosa, two case reports and diagnostic approach to lip swelling

open access: yesAdvances in Oral and Maxillofacial Surgery, 2022
Granulomatous cheilitis is a rare inflammatory condition, characterized by a consistent painless swelling of one or both lips, it is considered a monosymptomatic form of Melkersson-Rosenthal syndrome.
Soukaïna Oujdad   +3 more
doaj   +2 more sources

Cheilitis granulomatosa

open access: yesDermatology Online Journal, 2011
Melkersson-Rosenthal Syndrome (MRS) is a rare syndrome that is characterized by a triad of facial paralysis, chronic edema of the lip, and a fissured tongue. Most commonly, one element of the triad precedes the development of the other symptoms. We present a case of cheilitis granulomatosa (CG) as a manifestation of incomplete MRS.
Rose, Amy E   +3 more
core   +9 more sources

Cheilitis granulomatosa: a review. [PDF]

open access: yesHead Neck Pathol, 2014
Cheilitis granulomatosa (CG) is a cosmetically disturbing and persistent idiopathic lip swelling. It is one manifestation of orofacial granulomatosis (OFG), which is a clinical entity describing facial and oral swelling in the setting of non-caseating granulomatous inflammation and in the absence of systemic disease such as Crohn's disease and ...
Critchlow WA, Chang D.
europepmc   +4 more sources

Coincidence of cheilitis granulomatosa and chronic spontaneous angioedema: successful treatment with dapsone and omalizumab

open access: yesJournal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2020
In 2016, a 25-year-old woman presented to our department with a seven-year history of recurrent swelling of the upper lip. She described the swelling as being continuously present and associated with periodic flares that usually lasted for several days ...
Alexandra Gronostay   +3 more
semanticscholar   +2 more sources

Factitious cheilitis: a case report

open access: yesJournal of Medical Case Reports, 2008
Introduction Factitious cheilitis is a chronic condition characterized by crusting and ulceration that is probably secondary to chewing and sucking of the lips. Atopy, actinic damage, exfoliative cheilitis, cheilitis granulomatosa or glandularis, contact
Aydin Erdinc   +3 more
doaj   +2 more sources

Cheilitis Granulomatosa- Report of two cases with clinical and diagnostic implications

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2006
Cheilitis granulomatosa is a rare inflammatory disorder of unknown origin. The clinical recognition of this condition is important as is the subsequent investigation by an appropriate specialist. Management considerations for these patients needs to take
Amar A Sholapurkar   +4 more
doaj   +1 more source

Cheilitis granulomatosa (Miescher granulomatous macrocheilitis) with Down syndrome: A rare alliance

open access: yesIndian Journal of Paediatric Dermatology, 2016
Melkersson–Rosenthal syndrome comprises of the triad of orofacial swelling, facial paralysis, and fissured tongue. It may present in monosymptomatic form as Meischer granulomatous cheilitis. Herein we report an unusual association of Meischer's cheilitis
Balwinder Kaur Brar   +2 more
doaj   +2 more sources

Cheilitis Granulomatosa

open access: yesNishi Nihon Hifuka, 1978
• Cheilitis granulomatosa is a rare condition that has traditionally proved difficult to treat satisfactorily. Excellent results were obtained in our case with local triamcinolone acetonide injections and surgery. Histopathologic features of the classic, untreated condition were reviewed and compared to the histopathologic features of labial tissues ...
David Krutchkoff
core   +3 more sources

Unraveling angioedema: diagnostic challenges and emerging therapies [PDF]

open access: yesFrontiers in Immunology
Bradykinin-mediated angioedema comprises rare but potentially life-threatening disorders, most notably hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency or dysfunction.
Felix Johnson, Benedikt Hofauer
doaj   +2 more sources

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