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Pseudocyst of the auricle, also known as auricular pseudocyst, endochondral pseudocyst, cystic chondromalacia, intracartilaginous auricular seroma cyst, and benign idiopathic cystic chondromalacia, [1] is a cutaneous condition characterized by a fluctuant, tense, noninflammatory swelling on the upper half of the ear, known as the auricle or pinna.
Preauricular sinuses and cysts result from developmental defects of the first and second pharyngeal arches. [10] This and other ear malformations are sometimes associated with renal anomalies. [ 11 ] In rare circumstances these pits may be seen in genetic conditions such as branchio-oto-renal syndrome ; however these conditions are always ...
Scan of Figure 2, from Darwin's Descent of Man, second edition, illustrating Darwin's tubercle. This atavistic feature is so called because its description was first published by Charles Darwin in the opening pages of The Descent of Man, and Selection in Relation to Sex, as evidence of a vestigial feature indicating common ancestry among primates which have pointy ears.
A cauliflower ear deformity. Inflammation of the cartilage of the ear is a specific symptom of the disease and affects most people. [3] It is present in about 20% of persons with RP at presentation and in 90% at some point. [3] Both ears are often affected but the inflammation may alternate between either ear during a relapse. [3]
Vocal fold cysts (also known as vocal cord cysts) are benign masses of the membranous vocal folds. [1] These cysts are enclosed, sac-like structures that are typically of a yellow or white colour. [2] They occur unilaterally on the midpoint of the medial edge of the vocal folds. [1] They can also form on the upper/superior, surface of the vocal ...
cyst [7] skin tag [7] sunburn, frostbite [6] pressure ulcer, often from a poorly fitting hearing aid [6] anotia, absent pinna [7] microtia, underdeveloped pinna [7] cryptotia, a pinna covered beneath the skin of the scalp [5] Stahl's deformity, pointed pinna due to an extra fold of cartilage [5] cupped or constricted ear deformity, a hooded ...
The cyst wall is composed of squamous epithelium (90%), columnar cells with or without cilia, or a mixture of both, with lymphoid infiltrate, often with prominent germinal centers and few subcapsular lymph sinuses. The cyst is typically surrounded by lymphoid tissue that has attenuated or absent overlying epithelium due to inflammatory changes.
Not all middle ear epidermal cysts are congenital, as they can be acquired either by metaplasia of the middle ear mucosa or by traumatic implantation of ear canal or tympanic membrane skin. In addition, cholesteatoma inadvertently left by a surgeon usually regrows as an epidermal cyst. Some authors have also suggested hereditary factors. [9] [10]