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The difference between them is that a cyst does not connect with the skin, but a sinus does. [3] Frequency of preauricular sinus differs depending the population: 0.1–0.9% in the US, 0.9% in the UK, and 4–10% in Asia and parts of Africa. [4] Preauricular sinuses are inherited features, and frequently appear next to both ears. [5]
It is called preauricular sinus which, according to the U.S. National Institutes of Health, or NIH, "generally appears as a tiny skin-lined hole or pit, often just in front of the upper ear where ...
C. Calcifying epithelioma of Malherbe; Capillary hemangioma; Cephalic brain-like heterotopia; Cervical accessory tragus; Congenital absence of skin; Congenital auricular fistula
In anatomy, a fistula (pl.: fistulas or fistulae /-l i,-l aɪ /; from Latin fistula, "tube, pipe") is an abnormal connection (i.e. tube) joining two hollow spaces (technically, two epithelialized surfaces), such as blood vessels, intestines, or other hollow organs to each other, often resulting in an abnormal flow of fluid from one space to the other.
The several components or degrees of development range from an ear tag, preauricular appendage, preauricular tag, or accessory tragus, to supernumerary ears or polyotia. [7] It is a relatively common congenital anomaly of the first branchial arch or second branchial arches.
Otofaciocervical syndrome, also known as Fara Chlupackova syndrome, [1] are a small group of rare developmental disorders of genetic origin which are characterized by facial dysmorphisms, long neck, preauricular and/or branchial pits, cervical muscle hypoplasia, hearing loss, and mild intellectual disabilities.
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The preauricular deep parotid lymph nodes (anterior auricular glands or preauricular glands), from one to three in number, lie immediately in front of the tragus. Their afferents drain multiple surfaces, most of which are lateral in origin.