Results 141 to 150 of about 1,199,438 (182)
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Seminars in Dermatology, 1995
Melkersson-Rosenthal syndrome is a triad of recurrent orofacial swelling, relapsing facial paralysis, and fissured tongue. However, the classic triad is not frequently seen in its complete form. Monosymptomatic and oligosymptomatic forms are more common. The histological findings of sarcoid-like granuloma in skin or mucosal biopsy specimens support the
M S, Daoud, R S, Rogers
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Melkersson-Rosenthal syndrome is a triad of recurrent orofacial swelling, relapsing facial paralysis, and fissured tongue. However, the classic triad is not frequently seen in its complete form. Monosymptomatic and oligosymptomatic forms are more common. The histological findings of sarcoid-like granuloma in skin or mucosal biopsy specimens support the
M S, Daoud, R S, Rogers
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Otolaryngology–Head and Neck Surgery, 2008
OBJECTIVESTo study characteristics of Melkersson‐Rosenthal syndrome (MRS) patients with facial palsy (FP) and differences in patients treated at the Departments of Otorhinolaryngology and Dermatology.METHODSClinical picture of MRS was studied from patient charts at two departments. Patients with FP received a questionnaire and were examined.
Mervi, Kanerva +4 more
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OBJECTIVESTo study characteristics of Melkersson‐Rosenthal syndrome (MRS) patients with facial palsy (FP) and differences in patients treated at the Departments of Otorhinolaryngology and Dermatology.METHODSClinical picture of MRS was studied from patient charts at two departments. Patients with FP received a questionnaire and were examined.
Mervi, Kanerva +4 more
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The Journal of Laryngology & Otology, 2002
Melkersson-Rosenthal syndrome (MRS) is a rare idiopathic non-caseating granulomatous condition. It is rarely described in otorhinolaryngology-related journals, although facial palsy, lip-swelling, and lingua plicata, are its most common presenting features. This classical triad however is not always present in MRS.
K L, Ang, N S, Jones
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Melkersson-Rosenthal syndrome (MRS) is a rare idiopathic non-caseating granulomatous condition. It is rarely described in otorhinolaryngology-related journals, although facial palsy, lip-swelling, and lingua plicata, are its most common presenting features. This classical triad however is not always present in MRS.
K L, Ang, N S, Jones
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Melkersson - Rosenthal Syndrome
Archives of Dermatology, 1961The Melkersson-Rosenthal syndrome is an unusual condition which, except for a few isolated reports in otolaryngologic journals, is rarely described in American medical literature. It comprises a triad consisting of recurrent facial paralysis, intermittent facial edema which subsequently becomes permanent, and lingua plicata.
S, WALLK, S M, BLUEFARB
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The Melkersson-Rosenthal Syndrome
Pediatrics, 1984The Melkersson-Rosenthal syndrome consists of recurrent swelling of the lip or face, intermittent facial palsy, and fissured tongue. Lengthy intervals may occur between those various manifestations. Four white female patients with this disorder are described. First identified in Europe, the condition is now increasingly recognized in this country.
W B, Wadlington, H D, Riley, L, Lowbeer
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Pamukkale Medical Journal, 2023
The Melkersson-Rosenthal syndrome (MRS) is a rare neuro mucocutaneous granulomatous disease presenting with recurrent peripheral facial paralysis, orofacial oedema, and fissured tongue. The coexistence of the classic clinical triad is rare. Clinical findings and examination make the diagnosis.
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The Melkersson-Rosenthal syndrome (MRS) is a rare neuro mucocutaneous granulomatous disease presenting with recurrent peripheral facial paralysis, orofacial oedema, and fissured tongue. The coexistence of the classic clinical triad is rare. Clinical findings and examination make the diagnosis.
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Southern Medical Journal, 1986
We have described a 35-year-old woman who had had recurrent episodes of swelling of the lips since the age of 14. The patient had a complete remission of symptoms between the ages of 20 to 30, but the swelling recurred, and she has had permanent swelling of both lips and cheeks for the past four years. Various treatments were ineffective. Biopsy of the
P, Langevitz +3 more
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We have described a 35-year-old woman who had had recurrent episodes of swelling of the lips since the age of 14. The patient had a complete remission of symptoms between the ages of 20 to 30, but the swelling recurred, and she has had permanent swelling of both lips and cheeks for the past four years. Various treatments were ineffective. Biopsy of the
P, Langevitz +3 more
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Journal of Cutaneous Pathology, 2005
A 13 year‐old boy presented with a six‐month history of severe lip swelling. His past medical history was significant for eczema, multiple episodes of urticaria, and two episodes of anaphylaxis. Physical exam revealed severe cheilitis and labial angioedema. The cranial nerves were intact, and there was no evidence of a fissured tongue.
S. Estrada, R. Trepeta
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A 13 year‐old boy presented with a six‐month history of severe lip swelling. His past medical history was significant for eczema, multiple episodes of urticaria, and two episodes of anaphylaxis. Physical exam revealed severe cheilitis and labial angioedema. The cranial nerves were intact, and there was no evidence of a fissured tongue.
S. Estrada, R. Trepeta
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