Chin Augmentation in Cyprus

Chin Augmentation in Cyprus section, includes general infrmation about Chin Augmentation Procedure, Chin Augmentation Cyprus Local News, Chin Augmentation Cyprus Surgeon Locator and other Chin Augmentation related material.


Chin Augmentation Procedure


Plastic surgeons use implants to emphasize your face. The implants will create a harmonic appearance of your face allowing you to feel better about yourself. There are many types of implants made of different material. They can emphasize the jaw line, the checks and create a better proportions between the chin and the checks.

The surgeons use implants to achieve a better balance and create a younger look. Chin augmentation also called mentoplasty. The operation aimed to shape the chin by making it smaller or bigger. A larger chin can be created by an implant insertion or by surgery, which elongates the lower jaw. Smaller chin is made by reducing the size of the lower jaw. In many cases the surgeon will recommend mentoplasty for patients undergoing nose surgery in order to fit the new nose to the face, creating more harmonic appearance. When looked from the side the nose size should fit the chin.

The implant insertion may last from 30 minutes to one hour. The surgeon will design the implant that fits your chin and then inserted it to a "pocket" located in front of the chin. A small cut for the insertion can be made inside the mouse near the lower lip or from the outside just below the chin. After the procedure the chin is bandaged using plasters to prevent swelling and implant movement. Bandages also help prevent uncomfortable felling. The stitches can be removed after 5-7 days. In case the cut is made inside the mouse melting stitches are used and there is no need to remove them. The surgery can be done using local anesthetics with sedative drugs and sometimes with general anesthesia.

Every operation has its ricks. The implant may move from the original place. Then you need to undergo additional procedure to replace it. Infection is rare, it can be treated with antibiotics and in some cases the infected implant will be removed and replaced by another one.

After the surgery there is a strange felling around the chin. It is normal to fell difficulties in talking, smiling and eating. There may be blue marks around the chin and neck. It is advisable not to participate in activities which may harm the chin. The surgeon will guide you regarding dental hygiene and eating.

The final results may take weeks and even month to notice, therefore you must be patient.

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More Cyprus info...


  • Cyprus Cities

    Note that Cypriot cities have a variety of historical spellings and writings, all in fairly common use, and which change according to the context, whether it be Greek Cypriot, Turkish or English tourist. The following list emphasizes traditional English spellings, that will most often be encountered by the traveller.


    Nicosia (also Nikosia, Lefkosia "Lefkosa") - the divided capital
    Larnaca Larnaka
    Limassol Lemesos "Limasol"
    Paphos Pafos "Baf"

  • Cyprus By plane

    Cyprus' main airport is Larnaca International Airport (LCA) and is located on the outskirts of Larnaka.

    The previous main international airport located SW of Nicosia is now located on the Green Line separating the Greek and Turkish parts of Cyprus - it has been out of use since 1974.

    Cyprus is serviced by a variety of different carriers, the main one being the Cypriot Cyprus Airways. There are flight connections with most major European towns, e.g. London, Birmingham, Manchester, Frankfurt, Paris, Amsterdam, Rome, Milan) and many Eastern European countries. Unfortunately almost all non-Cyprus Airways scheduled flights arrive and depart in the middle of the night (2/3 o'clock). There are also connections to almost all Middle Eastern capitals. There are no flights to Turkey from the south.

    There are also charter flights to the western airport of Paphos.

Plastic Surgery News...

  • The National Institute for Health and Clinical Excellence (NICE) in association with the National Collaborating Centre for Cancer have published guidelines on the diagnosis and treatment of prostate cancer. The guidelines make recommendations on treatment options for localised prostate cancer, managing relapse after radical surgery, managing locally advanced prostate cancer, and treatment options for metastatic prostate cancer. The guidelines discuss the evidence supporting the use of the following options for metastatic prostate cancer: • Hormonal therapy • Androgen withdrawal versus combined androgen blockade (CAB) - Combined androgen blockade is not recommended as a first-line treatment for men with metastatic prostate cancer. • Anti-androgen monotherapy - For men with metastatic prostate cancer who are willing to accept the adverse impact on overall survival and gynaecomastia in the hope of retaining sexual function, antiandrogen monotherapy with bicalutamide (150 mg) is appropriate. • Intermittent androgen withdrawal - Intermittent androgen withdrawal may be offered to men with metastatic prostate cancer providing they are informed that there is no long-term evidence of its effectiveness. • Managing complications of hormonal therapy • Hormone-refractory prostate cancer • Chemotherapy with docetaxel • Oestrogens and steroids • Bone targeted therapy - The use of bisphosphonates to prevent or reduce the complications of bone metastases in men with hormone-refractory prostate cancer is not recommended. Bisphosphonates for pain relief may be considered for men with hormone-refractory prostate cancer when other treatments (including analgesics and palliative radiotherapy) have failed. • Palliative care
  • The Southwest Oncology Group Study 9626 has examined the efficacy of megesterol acetate (MA) in treating hot flushes in women with breast cancer. It involved 288 patients (2 ineligible) with T1-3, N0-1, M0 breast cancer who had completed surgery and chemotherapy and at least 4 months of tamoxifen (if prescribed). They had to have experienced at least 10 hot flushes of any severity or at least five severe episodes per week. Overall, 85% were on tamoxifen, 40% had over 63 hot flushes per week and 75% had vasomotor symptoms for 6 months or longer. They were randomised to receive placebo (n=101), MA 20 mg (n=92), or MA 40 mg (n=93) for 3 months. Success at 3 months was defined as completion of treatment with a 75% or greater reduction in hot flushes from baseline. Another 3 months of treatment was given in the same blinded arm if success was achieved, and in those who were not classified as successfully treated, open-label MA 20 mg was added to blinded study drug and continued for 3 months. Success at 3 months was reported in: • 14% on placebo • 65% on 20 mg (p < 0.0001 vs placebo) • 48% on 40 mg (p < 0.0001 vs placebo) In addition, most successes at 3 months were maintained at 6 months (77% on 20 mg and 81% on 40 mg). There was however no significant impact on other menopausal symptoms. In physicians’ assessment of toxicity experienced by patients up to and including the 3-month evaluation, oedema and weight gain was reported in the placebo arm; fatigue in the MA20 arm; and depression, fatigue, nausea, and weight gain in the MA40 arm. There were no statistically significant differences by treatment arm for any toxicities. The researchers concluded that MA at the preferred dose of 20mg was successful in alleviating vasomotor symptoms in breast cancer survivors with durable results at 6 months. They suggest that “this treatment could be considered in women refractory to non-hormonal therapies whose symptom status is impaired by the vasomotor symptoms and who have been informed of the risk and benefit of such treatment by their physician.”

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