|IMAGES IN CLINICAL PRACTICE
|Year : 2015 | Volume
| Issue : 6 | Page : 651
Blepharochalasis with double lip: A case of Ascher syndrome
Vishal Gupta, Sujay Khandpur
Department of Dermatology and Venereology, All India Institute of Medical Sciences, New Delhi, India
|Date of Web Publication||28-Oct-2015|
Dr. Sujay Khandpur
Department of Dermatology and Venereology, Fourth Floor, Teaching Block, All India Institute of Medical Sciences, Ansari Nagar, New Delhi - 110 029
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Gupta V, Khandpur S. Blepharochalasis with double lip: A case of Ascher syndrome. Indian J Dermatol Venereol Leprol 2015;81:651
|How to cite this URL:|
Gupta V, Khandpur S. Blepharochalasis with double lip: A case of Ascher syndrome. Indian J Dermatol Venereol Leprol [serial online] 2015 [cited 2020 Jun 5];81:651. Available from: http://www.ijdvl.com/text.asp?2015/81/6/651/158645
A 12-year-old boy presented with recurrent upper eyelid swelling since 2 years of age. Examination showed edema and laxity of both upper eyelids and loose mucosa hanging from the inner aspect of the upper lip ('double upper-lip') [Figure 1] suggestive of Ascher syndrome.
|Figure 1: Edema affecting both upper eyelids and redundant fold of mucosa hanging from upper lip giving the appearance of 'double lip'|
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Ascher syndrome is characterized by blepharochalasis, double lip and non-toxic goiter but all the features may not be seen in every case. It can be confused with Melkersson–Rosenthal syndrome, hereditary angioedema, early-onset dermatochalasis and acquired cutis laxa. Mounier–Kuhn syndrome can also have similar features, in addition to congenital tracheo-bronchomegaly. The treatment is surgical correction of the deformities.
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