scholarly journals Lymphangioma circumscriptum Associated with Port-Wine Stain

2019 ◽  
Vol 2 (1) ◽  
pp. 93-95
Author(s):  
Nidhi Shah ◽  
A Rijal ◽  
S Agrawal
Keyword(s):  
Pregnant Female ◽  
Port Wine Stain ◽  
Port Wine ◽  
Benign Disorder ◽  
Biopsy Report ◽  
Lymphangioma Circumscriptum ◽  
One Year ◽  
The Right

Lymphangioma circumscriptum (LC) is a rare benign disorder involving the deep dermal and subcutaneous lymphatic channels. We present a case of a 32-year old 26 weeks pregnant female with multiple fluid filled vesicles over the vulvae of one year duration with itching. The lesions had increased in size after the onset of pregnancy. The patient also had a large port-wine stain (PWS) over the right buttock extending up to the perineum. The biopsy report was consistent with LC.

scholarly journals Gingival Tissue Alterations in 2 Patients with Port Wine Stain

2014 ◽  
Vol 18 (2) ◽  
pp. 109-112
Author(s):  
Ayse Kocak-Buyukdere ◽  
Esra Guzeldemir
Keyword(s):  
Soft Tissue ◽  
Gingival Tissue ◽  
Port Wine Stain ◽  
Port Wine ◽  
Wisdom Tooth ◽  
Upper Jaw ◽  
Vascular Birthmarks ◽  
The Right ◽  
Tissue Alterations ◽  
Nevus Flammeus

SUMMARYNevus flammeus, which is also known as port-wine stain (PWS), is one of the vascular birthmarks. PWS occurs in 0.3% of the newborns in both genders. It is a capillary vascular malformation, characterized by a pink or red stain and may involve skin, soft tissue and/or bone. There are a very limited number of reports regarding intraoral involvement of PWS. We report 2 female patients with PWS from date of birth. The first patient was an 11-year-old female who applied to our clinics for the treatment of her non-aesthetic and deviated intraoral view and discoloration of her gingiva, and the second patient was a 56-year-old female who applied for the extraction of her wisdom tooth. Extraoral examination in both patients revealed a diffuse PWS on the right side of their face over the cheek, extending from the midline. While the first patient had reddish skin, gingiva on right site her both jaws and lips, the second patient had only her upper jaw and lip. Because of the first patient’ age, the treatment postponed to her 20’, and the second patient did not accept any treatment. PWS is a rare and non-fatal condition; however, the unique appearance of these patients can lead to psychological problems especially in early ages.

Endocrine Dysfunction in a Patient With Phace Syndrome, Including Port-Wine Stain of the Right Periorbital Area

2010 ◽  
Vol 16 (2) ◽  
pp. 255-259 ◽  
Author(s):  
Marie Merheb ◽  
Roula Hourani ◽  
Mira Zantout ◽  
Sami Azar
Keyword(s):  
Port Wine Stain ◽  
Port Wine ◽  
Endocrine Dysfunction ◽  
Phace Syndrome ◽  
The Right

scholarly journals Acquired Port-Wine Stain Following Minor Trauma: Fegeler Syndrome

2019 ◽  
Vol 31 (Suppl) ◽  
pp. S5
Author(s):  
Geun-Hwi Park ◽  
Woo-Il Kim ◽  
Min-Young Yang ◽  
Won-Ku Lee ◽  
Tae-Wook Kim ◽  
...  
Keyword(s):  
Minor Trauma ◽  
Port Wine Stain ◽  
Port Wine

scholarly journals Periodontal Management of Sturge-Weber Syndrome

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Butchibabu Kalakonda ◽  
Koppolu Pradeep ◽  
Ashank Mishra ◽  
Krishnanjaneya Reddy ◽  
Tupili Muralikrishna ◽  
...  
Keyword(s):  
Oral Manifestations ◽  
Port Wine Stain ◽  
Scaling And Root Planing ◽  
Port Wine ◽  
Ocular Abnormalities ◽  
Parietal Lobes ◽  
Gingival Enlargement ◽  
Weber Syndrome ◽  
Sturge Weber Syndrome ◽  
Neurocutaneous Syndromes

Sturge-Weber syndrome (SWS) is a sporadic disorder and is frequent among the neurocutaneous syndromes specifically with vascular predominance. This syndrome consists of constellation of clinical features like facial nevus, seizures, hemiparesis, intracranial calcifications, and mental retardation. It is characterized by focal port-wine stain, ocular abnormalities (glaucoma), and choroidal hemangioma and leptomeningeal angioma most often involving occipital and parietal lobes. The present paper reports three cases of SWS with oral manifestations and periodontal management, which included thorough scaling and root planing followed by gingivectomy with scalpel and laser in cases 1 and 3 consecutively to treat the gingival enlargement. However, the treatment in case 2 was deferred as the patient was not a candidate for periodontal surgery.

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