Results 41 to 50 of about 1,199,438 (182)
Cheilitis granulomatosa (Miescher granulomatous macrocheilitis) with Down syndrome: A rare alliance
Indian 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 +1 more source
A Case of Melkersson-Rosenthal Syndrome Treated With 5-FU
Ear, Nose & Throat Journal, 2021 The rarity of Melkersson-Rosenthal syndrome, or orofacial granulomatosis, can present with persistent midface bogginess. The management for previous reported cases has included corticosteroid injections, antihistamines, and antibiotics.
David M. Alessi MD +2 more
doaj +1 more source
Melkersson‐Rosenthal‐syndrome ‐ A Rare Case of Laryngeal Involvement
, 2022 The Laryngoscope, Volume 132, Issue 12, Page 2442-2444, December 2022.
Nina Wenda +4 more
wiley +1 more source
Rossolimo–Melkersson–Rosenthal syndrome in 14 years old child with Down`s syndrome. Case report
, 2023 Rossolimo–Melkerson–Rosenthal syndrome is not so often diagnosed in childhood. It is noted that children's syndrome occurs as a monosymptom in the form of macrocheilitis.
Ekaterina V. Zadionchenko +1 more
core +1 more source
Syndrome de Melkersson-rosenthal: une entité rare à ne pas méconnaitre
The Pan African Medical Journal, 2015 Le syndrome de Melkersson-Rosenthal est une entité clinique rare, définie par la triade oedème oro-facial, paralysie faciale récurrente et langue plicaturée. Cette triade peut être incomplète ou apparaître de manière différée dans le temps. Le diagnostic
Rim Klii, Wafa Chebb
doaj +1 more source
Allergy, Volume 81, Issue 8, Page 2744-2774, August 2026.ABSTRACT Hereditary angioedema (HAE) with C1 inhibitor deficiency is a rare disease characterized by unpredictable episodes of tissue swelling (angioedema), which, in most cases, occur first under the age of 18 years, and entail a significant burden of disease not only for the patients but also for their families.
Henriette Farkas +128 more
wiley +1 more source
Melkersson–Rosenthal Syndrome: A Case Report
Southern Clinics of Istanbul Eurasia, 2018 Melkersson-Rosenthal Syndrome (MRS) is a rare disease characterized by the triad of recurring facial paralysis, a fissured tongue, and recurring swelling of the lips and/or face.
Sedat Aydın +4 more
doaj +1 more source
Chronic Lower Lip Swelling due to Granulomatous Cheilitis
Clinical Case Reports, Volume 14, Issue 5, May 2026.ABSTRACT Granulomatous cheilitis should be considered in the differential diagnosis of persistent, unexplained orofacial swelling, particularly when standard treatments fail.
Jesus Ruiz, Jacob Garner
wiley +1 more source
Síndrome de Melkersson-Rosenthal [PDF]
, 2019 Melkersson-Rosenthal syndrome is an affection of unknown origin, characterized by a classic triad: recurrent oro-facial swelling, recurrent peripheral facial paralysis and fissured tongue.
Marini3, Mario Alberto +3 more
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Melkersson-Rosenthal syndrome: Still arousing clinician interest! [PDF]
, 2021 Melkersson–Rosenthal syndrome (MRS) is a rare neuromucocutaneous syndrome. It is a rare orofacial granulomatosis of controversial etiology, marked by the triad of recurrent nonpitting orofacial edema, recurrent facial palsy and plicated tongue.
Rkiouak, Adil +2 more
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