M103 UNDER THE MASQUERADE OF ANGIOEDEMA, CHEILITIS GRANULOMATOSA AN IMPORTANT CLINICAL CONSIDERATION

2021 ◽  
Vol 127 (5) ◽  
pp. S83
Author(s):  
L. Maurer ◽  
N. Mambetsariev ◽  
M. Watts ◽  
C. Saltoun ◽  
F. Kuang
Keyword(s):  
Clinical Consideration ◽  
Cheilitis Granulomatosa

Cheilitis granulomatosa

1966 ◽  
Vol 94 (5) ◽  
pp. 660-661
Author(s):  
M. A. Storkan
Keyword(s):  
Cheilitis Granulomatosa

Cheilitis Granulomatosa Miescher: Treatment with Clofazimine and Review of the Literature

2001 ◽  
Vol 110 (10) ◽  
pp. 964-967 ◽  
Author(s):  
Gerd Jürgen Ridder ◽  
Milo Fradis ◽  
Erwin Löhle
Keyword(s):  
Differential Diagnosis ◽  
Young Woman ◽  
Alternative Treatment ◽  
Rare Condition ◽  
Review Of The Literature ◽  
Cheilitis Granulomatosa ◽  
Methods Of Treatment

Cheilitis granulomatosa Miescher is a rare condition of unknown cause characterized by intermittent lip swelling that gradually persists and causes cosmetic deformity. We report the case of a young woman with cheilitis granulomatosa as a monosymptomatic manifestation of Melkersson-Rosenthal syndrome successfully treated by the antileprosy agent clofazimine, and propose clofazimine as an alternative treatment in cases refractory to corticosteroids. The differential diagnosis and current methods of treatment are summarized, and the literature is reviewed and discussed.

Cheilitis granulomatosa

2011 ◽  
Vol 17 (10) ◽  
Author(s):  
Amy E Rose ◽  
Marie Leger ◽  
Julie Chu ◽  
Shane Meehan
Keyword(s):  
Cheilitis Granulomatosa

scholarly journals Adenomatoid Tumor of Testis

2009 ◽  
Vol 2 ◽  
pp. CPath.S3091 ◽  
Author(s):  
Waqas Amin ◽  
Anil V. Parwani
Keyword(s):  
Wilms Tumor ◽  
Frozen Section ◽  
Benign Tumors ◽  
Excision Biopsy ◽  
Clinical Consideration ◽  
Fibrous Stroma ◽  
Beta Hcg ◽  
Columnar Cells ◽  
Slow Growing ◽  
Vacuolated Cytoplasm

Adenomatoid tumors are responsible for 30% of all paratesticular masses. These are usually asymptomatic, slow growing masses. They are benign tumors comprising of cords and tubules of cuboidal to columnar cells with vacuolated cytoplasm and fibrous stroma. They are considered to be of mesothelial origin supported by histochemical studies and genetic analysis of Wilms tumor 1 gene expression. Excision biopsy is both diagnostic and therapeutic procedure. The main clinical consideration is accurate diagnosis preventing unnecessary orchiectomy. Diagnostic studies include serum tumor markers (negative alpha fetoprotein, beta HCG, LDH) ultrasonography (hypoechoic and homogenous appearance) and frozen section.

Leaking Labyrinth Lesions, Deafness, Tinnitus and Dizziness

1981 ◽  
Vol 90 (2) ◽  
pp. 99-106 ◽  
Author(s):  
Victor Goodhill
Keyword(s):  
Clinical Consideration ◽  
Membranous Labyrinth ◽  
Congenital Origin ◽  
Intracranial Complications

The remarkable integrity of the finely balanced membranous labyrinth is occasionally disrupted, resulting in fistulae of various types in a number of locations. Such leaking labyrinth lesions can be of congenital origin, due to various types of malformations. They may be caused by destructive diseases such as syphilis, by many variants of acute and chronic otomastoiditis, and sequelae of otosclerosis surgery, and finally, as results of a variety of traumatic disruptions of labyrinthine integrity. Deafness, dizziness, and tinnitus are frequent symptoms and sequelae may include meningitis and other intracranial complications. The clinical consideration of leaking labyrinth lesions must always be considered in otologic diagnoses.

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