Loading…

Congenital midline sinus of the upper lip: A case report and review of literature

•Very rare case report, isolated congenital upper lip midline sinus.•Surgical excision is curative, no recurrence.•Upper lip midline sinus can be associated with syndromes or conditions. Congenital pits of the lip are uncommon and may be associated with conditions such as Van der Woude syndrome. Iso...

Full description

Saved in:
Bibliographic Details
Published in:International journal of surgery case reports 2018-01, Vol.51, p.41-44
Main Authors: Salah, Bareqa I., Al-Rawashdeh, Baeth, Al-Ali, Zaid R., Mahseeri, Mohamad, Al-Zu’bi, Zayed
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:•Very rare case report, isolated congenital upper lip midline sinus.•Surgical excision is curative, no recurrence.•Upper lip midline sinus can be associated with syndromes or conditions. Congenital pits of the lip are uncommon and may be associated with conditions such as Van der Woude syndrome. Isolated lip pits are extremely rare developmental defects. A 7 year old Caucasian girl presented to plastic surgery clinic in Jordan University academic hospital complaining of an upper lip pit that has been present since birth. It was associated with a single episode of whitish discharge. On examination, an isolated upper lip midline sinus was found. She is otherwise fit and healthy. Surgical excision was curative with good cosmetic outcome. The prevalence of lower lip sinuses has been estimated to be about 0.00001% of the white population. Upper lip sinuses are even more uncommon. To date, there have been several case reports of upper lip sinuses and fistulas. A total of 55 cases was found upon reviewing the English literature. No similar cases were reported in Jordan. Different presentations are mentioned in this review. Several embryologic theories are presented. Upper lip sinus formations are rare developmental events, and the pathogenesis of these lesions still needs further evaluation. Simple surgical excision is the treatment of choice.
ISSN:2210-2612
2210-2612
DOI:10.1016/j.ijscr.2018.08.012