Results 31 to 40 of about 1,199,438 (182)

Oral lichen planus and related lesions. What should we accept based on the available evidence?

open access: yesOral Diseases, Volume 29, Issue 7, Page 2624-2637, October 2023., 2023
Abstract Recent new terminologies have been proposed for lesions in the sphere of oral lichen planus (OLP) that theoretically present unique aetiological, clinical, prognostic or management characteristics different from those of the so‐called typical forms of OLP.
Miguel Ángel González‐Moles   +1 more
wiley   +1 more source

Facial Palsy in a Child with a History of Cheilitis Granulomatosa: Melkersson–Rosenthal Syndrome

open access: yesB-ENT, 2023
Melkersson–Rosenthal syndrome is a rare neuromucocutaneous granulomatous syndrome of unknown etiology characterized by a classical triad of relapsing orofacial edema, recurrent peripheral facial palsy, and lingua plicata.
Chloë Surmont   +7 more
doaj   +2 more sources

Sarcoidosis and its oral manifestations: A case report study

open access: yesClinical Case Reports, Volume 11, Issue 2, February 2023., 2023
Abstract A patient was referred to the oral medicine department with redness and swelling of the lips and cheek, and an intra‐oral lesion. Biopsy and laboratory investigations suggested a diagnosis of sarcoidosis. In this study we discuss oral findings associated with sarcoidosis.
Mehdi Shahabinejad   +3 more
wiley   +1 more source

Primary Tuberculosis of Buccal and Labial Mucosa: Literature Review and a Rare Case Report of a Public Health Menace

open access: yesCase Reports in Dentistry, Volume 2023, Issue 1, 2023., 2023
Tuberculosis (TB) is a chronic granulomatous infectious disorder, caused by Mycobacterium tuberculosis. Despite the recent advancements in antitubercular therapy (ATT), it remains a global public health concern. TB is a leading infectious cause of global mortality, second only to coronavirus disease 2019 (COVID‐19). TB of the oral cavity is an uncommon
Shyamkumar Sriram   +5 more
wiley   +1 more source

Impact of off‐label use regulations on patient care in dermatology – a prospective study of cost‐coverage applications filed by tertiary dermatology clinics throughout Germany

open access: yesJournal of the European Academy of Dermatology and Venereology, Volume 36, Issue 11, Page 2241-2249, November 2022., 2022
Abstract Background In dermatology, a medical speciality with a relatively high number of rare diseases, physicians often have to resort to off‐label treatment options. To avoid claims, physicians in Germany can file a cost‐coverage request (off‐label application, OL‐A).
R.N. Werner   +15 more
wiley   +1 more source

Rossolimo–Melkersson–Rosenthal syndrome as a manifestation of lip sarcoidosis [PDF]

open access: yesVestnik Dermatologii i Venerologii, 2022
A 38-year-old female patient complained of lip augmentation. With a preliminary diagnosis of RossolimoMelkerssonRosenthal syndrome (monosymptomatic form), chronic fissure of the lower lip, the patient was sent for examination in order to exclude tumor ...
Yuri N. Perlamutrov   +4 more
doaj   +1 more source

Melkersson-rosenthal syndrome associated with hemifacial spasm [PDF]

open access: yes, 2017
Melkersson-Rosenthal Syndrome, with findings of repeating facial paralysis, orofacial edema, and fissured tongue, is rarely seen clinically.  We present the case of a 49-year-old female patient diagnosed with Melkersson-Rosenthal Syndrome, with the ...
Komurcu, Hatice Ferhan, Anlar, Omer
core   +1 more source

Rossolimo–Melkersson–Rosenthal syndrome in a 12-year-old adolescent: report of a rare case

open access: yesКлинический разбор в общей медицине, 2021
Rossolimo–Melkersson–Rosenthal syndrome is quite rare in children and adolescents 3–4 to 12–16 years of age. It most commonly occurs as a monosymptom in the form of macrocheilia.
Larisa I. Glebova   +2 more
doaj   +1 more source

A rare case of Melkersson–Rosenthal syndrome

open access: yesMedical Journal of Dr. D.Y. Patil Vidyapeeth, 2021
Melkersson–Rosenthal syndrome (MRS) is a rare clinical syndrome. The onset of illness usually occurs in the second decade of life. It is characterized by idiopathic facial paralysis and/or fissured tongue with oro-facial swelling, mainly lip edema.
Rajesh Verma, Rohit Anand
doaj   +1 more source

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