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Thread: Post-Auricular Cyst pictures - Ear Atlas

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    Default Post-Auricular Cyst pictures - Ear Atlas

    First branchial cleft anomalies are uncommon and comprise 1%–8% of all branchial cleft anomalies.1 They often present in the first two decades of life and present a clinical challenge as they can easily be misdiagnosed and thus inappropriately treated. They are thought to arise as a result of developmental abnormalities of the branchial apparatus and may take the form of a cyst, sinus, or fistula.

    Clinically they may present with repeated episodes of infection of the lesion. This may manifest itself with a cystic swelling or discharge from a fistulous opening either pre-auricularly or post-auricularly, in the cheek, or high in the neck. A thorough otological examination should be performed in all cases and may reveal a pit visible in the external canal at the site of entrance of a sinus or fistula. Such a lesion may result in otorrhoea or otitis externa with infective exacerbations. The meatus may be found to be partially or completely obstructed by bulging of the canal wall because of a cystic swelling. Such patients may complain of hearing loss, as may those with oedema associated with an otitis externa. There may however be a complete absence of signs in the external auditory canal. The patient may also give a history of having to repeatedly undergo incision and drainage of an apparent abscess around the ear because of infective exacerbations of the lesion that has not resolved.

    Early diagnosis and treatment are needed to avoid recurrent infection as scarring may cause difficulties with surgical dissection. Acute infective episodes should ideally be treated conservatively with antibiotics. However, this may not always be successful in settling the acute condition and referral for incision and drainage may still be required in some situations.

    Computed tomography with contrast will help define the extent of the lesion and identify extension into the middle ear.

    Surgical exploration and excision is the definitive treatment of these defects and should only be undertaken when any acute infective episode has cleared.

    In conclusion, cysts, sinuses, or fistulous tracts, which are pre-auricular or post-auricular or high in the neck may represent a branchial cleft anomaly. A high index of suspicion is required and a thorough otological examination and careful history should be . If suspected the patient should be referred for a specialist otological opinion as attempted drainage may complicate further definitive surgery.
    Post-Auricular Cyst pictures Atlas attachment.php?s=3f06cb27cd4d075b36ea1f9b14742b52&attachmentid=1877&d=1441394270

    Dermoid cyst can be histologically classified as dermoid cyst, epidermoid cyst, and teratoma, and it is known as proliferation of epithelial tissue of the congenital tumor, contained in the first pharyngeal arch (branchial arch) and medial epithelial seam of the second pharyngeal arch, but can occasionally be acquired. Dermoid cyst is a benign congenital tumor formed by cells abnormally separated at the period of fusion of viviparous tissues. The encapsulated cyst consists of stratified epithelium lined by laminated keratin material containing adnexal structures of skin, such as sebaceous gland, sweat gland, hair follicles, and hair It rarely occurs in the head and neck area and 7% of the overall prevalence has been reported to occur in the peripheral orbit, oral cavity, or nasal area, or in the center of the head and neck area . Epidermoid cyst is a common benign disease of the skin caused by inflammation of hair cortex follicles and proliferation of epidermal cells, and it can be congenital or acquired . Dermoid cyst and epidermoid cyst at the auricular area are extremely rare. Epidermoid cysts can also be acquired, and can be caused by various parts of the examination or after surgical operations, and in pediatric cases, determining whether an epidermoid cyst is congenital or acquired can be difficult. The authors experienced six cases of dermoid cyst and epidermoid cyst of the auricle; four cases were congenital and two cases were acquired. The cases of acquired cyst involved recurrence after surgery. In our institute, we experienced a relatively rare congenital and acquired dermoid cyst and epidermoid cyst of the auricle caused by several reasons and report different characteristics of each case with a review of the literature.

    Embryological dermoid cysts are assumed to occur when epithelial cells are isolated at the blockage of the pharyngeal arch of viviparous or implantation of epidermis into dermis due to penetrating injury . The origin of the auricle is formed by three hillocks at each side of the head and tail of the branchial arch, which is located between the first and second pharyngeal arch at six weeks of viviparous. These hillocks will be grown to form ears at seven weeks of viviparous. Histologically, dermoid cyst is composed of stratified squamous epithelium containing sebaceous glands and hair follicles, and adnexal structures of skin, such as laminated keratin material and hair, have been observed inside the cyst. Epidermoid cyst consisting of keratinous cyst and adnexal structures of skin was not observed. The other type is teratoma, which may include organs such as ectoderm, endoderm, mesoderm and adnexal structures of skin . However, all of these types are common and they contain laminated keratin material.

    Ikeda et al. reported two cases caused by outbreak of hillock at the auricle. These occurred since the outbreak of the auricle to form the upper part of the auricle of the fusion process of the first pharyngeal arch and to form an inclusion cyst, which causes dermoid cyst. This can be easily detected because it is located on the surface, however, it is sometimes found at the back of the helix cartilage located within the auriculocephalic sulcus. It is not found as a mass but appears as an auricle protruding toward the front but also in the form of a common mass On the other hand, the pathogenesis of epidermoid cyst has a variety of hypotheses; congenital epidermoid cyst will be caused by a shift of epithelial rests between 3 to 5 weeks of viviparous and mainly occur at the head and neck area. In the case of acquired epidermoid cyst, it is generated by blockage of hair cortex follicles, implementation of epidermis cell proliferation into the dermis due to penetrating injury The characteristic histologic array of cells at the follicular cyst wall consists of epidermal cells and granule cells in the origin of follicular infundibulum and filled with a cheese-like discharge, which is mainly fat. Therefore, it is not simply formed by trapping epidermal keratinocytes but also obstruction of the hair follicle wall just below the epidermis of skin cells, and together with sebum glands located within the papillary dermis under the skin, is known to be the main cause of epidermoid cyst; it can occur congenitally, however, an acquired epidermoid cyst causes significant confusion for both doctors and patients. In the current literature on epidermoid cysts that occurred after some kind of surgery, posttraumatic epidermoid cyst developed as a result of recent earlobe piercing of young people, and an acquired epidermoid cyst occurred after trauma through the skin from a subcutaneous scar tissue component of the trauma caused by accidental implantation. Epidermoid cyst after foreign body implantation or injection therapy or after cosmetic surgery has been reported . Cystic lesions occurring in the ear as a differential diagnosis are histologically dermoid cyst, epidermoid cyst, cystic teratoma, lipoma, hemangioma, branchial cyst, trichilemmal cyst, and keloids, and so on Most dermoid cysts at the auricle undergo surgery due to cosmetic reasons and surgery can also be performed for compression or irritation on the surrounding tissues and induction of inflammation. Incomplete removal may result in recurrence or infection, thus, complete surgical excision is necessary .

    The author experienced six cases in five patients with dermoid cyst and epidermoid cyst in the area of the ear. Congenital dermoid cyst occurred in four cases, and there were two cases of acquired dermoid cyst. Histologically, we had two cases with dermoid cyst and four cases with epidermoid cyst. Among four cases of congenital epidermoid cyst, three cases had a feature located on top of the helix. On the other hand, in the two cases of dermoid cyst, a mass was found at the auriculocephalic sulcus or back of the helix. The first three patients with epidermoid cysts were children with no history of trauma or surgery, thus, it is believed to be congenital.

    In case 1, epidermoid cyst possibly occurred over a period of 4 to 5 weeks in the first and second pharyngeal arch of six globules that fused together and ectodermal component was depressed between two and three prominentia The cyst was diagnosed histologically as an epidermoid cyst instead of a dermoid cyst, which can cause retardation in growth and development resulting in less developed adnexal structures of skin at the cysts. In addition, depressed cartilage can be observed at the bottom of the mass; this could be of the adjacent portion of bone of dermoid cyst accompanied by depressed bone. Even considering differences between the cases, this strongly suggests that epidermoid cyst occurred congenitally. Two cases occurred as acquired, the first case occurred one year after surgery for a congenital dermoid cyst, and the other case was an acquired epidermoid cyst after corrective cryptotia surgery. The first case was inflammation after surgery, possibly caused by residual tissues or cyst during the surgery and the possibility of remaining skin tissues or cystic tissues at perichondrium located at the bottom of the mass, and the possibility of surgical incision and engraftment of skin cells during the surgery was also considered. Therefore, surgery of these dermoid cysts requires close attention with control of inflammation. Finally, two cases of dermoid cyst were located at the auriculocephalic sulcus or back of the helix connecting to the hair part. It was considered to be looking at the occurrence of the auricle, which is formed within seven weeks of viviparous, when the auricle occurs for formation of the upper part of the helix of the fusion process of the first pharyngeal arch and in the surrounding tissues that formed an inclusion cyst that causes dermoid cyst.
    Post-Auricular Cyst pictures Atlas attachment.php?s=3f06cb27cd4d075b36ea1f9b14742b52&attachmentid=1878&d=1441394282

    Kim et al.experienced an acquired dermoid cyst, and did not report a difference between congenital dermoid cyst and acquired dermoid cyst. Unlike a congenital dermoid cyst surrounded by normal tissues, an acquired dermoid cyst was isolated, and surrounded by fibrous scar tissue. In addition, in this study, location of the mass has a significant value as it is associated with the occurrence of the auricle with the diagnosis of dermoid cyst at the ear. Particularly, in the case of an epidermoid cyst, history is important because it is difficult to prove histologically whether the cyst is congenital or acquired in the differential diagnosis. The authors emphasize that trauma or surgical procedure can cause acquired epidermoid cyst or acquired dermoid cyst, thus, a careful approach is required for access and report with literature review.

    :: ACFS :: Archives of Craniofacial Surgery

    Last edited by Medical Photos; 09-04-2015 at 07:18 PM.

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