48 cases of facial skin cancer (18 males, 30 females, aged 8-83 years) were admitted in Hue Central Hospital in 1996 – 2003 period. Among them, basocell cancers were common and leading causes on the face and neck areas. The disease occurred mainly in > 50 years old age, more common in female than in male, in rural people than in urban and most occurred in the centre of the face. Sun irradiation was the mainly important risk factor. Clinically, basocell cancer on the face was detected late with slow progress, little gland and no far metastasis. Basocell cancers had got good prognosis. Large removal the surrounding tissues and using local flap flexibly according the concrete site gave good outcomes functionally and esthetically.
Skin Neoplasms ; Case reports ; Maxillofacial Abnormalities ; Therapeutics

Computer Assisted Simulation Surgery (CASS) is a reliable method that permits oral and maxillofacial surgeons to visualize the position of the maxilla and the mandible as observed in the patient. The purpose of this report was to introduce a newly developed strategy for proximal segment management according to Balanced Orthognathic Surgery (BOS) protocol which is a type of CASS, and to establish the clinical feasibility of the BOS protocol in the treatment of complex maxillo-facial deformities. The BOS protocol consists of the following 4 phases: 1) Planning and simulation phase, 2) Modeling phase, 3) Surgical phase, and 4) Evaluation phase. The surgical interventions in 80 consecutive patients were planned and executed by the BOS protocol. The BOS protocol ensures accuracy during surgery, thereby facilitating the completion of procedures without any complications. The BOS protocol may be a complete solution that enables an orthognatic surgeon to perform accurate surgery based on a surgical plan, making real outcomes as close to pre-planned outcomes as possible.
Congenital Abnormalities ; Head* ; Humans ; Mandible ; Maxilla ; Methods* ; Oral and Maxillofacial Surgeons ; Orthognathic Surgery

Costello syndrome (CS) is a rare multiple congenital abnormality syndrome characterized by a typical coarse face, developmental delay, psychomotor and growth retardation, neurologic abnormalities, cardiac and cutaneous anomalies, severe feeding difficulties with postnatal growth failure, and increased risk of tumors. Since Costello first described it in 1971 and again in 1977, over 100 cases have been reported worldwide. It was recently shown that CS is a congenital condition caused by heterozygous de novo missense mutations affecting the codon for glycine 12 or 13 of the HRAS gene. We experienced three unrelated cases with coarse faces, developmental delays, short statures, macrocephaly, and redundant skin with deep palmar and plantar creases, hypertrophic cardiomyopathy and atrial tachycardia, which are characteristic of CS.
Cardiomyopathy, Hypertrophic ; Codon ; Congenital Abnormalities ; Costello Syndrome* ; Developmental Disabilities ; Glycine ; Macrocephaly ; Maxillofacial Abnormalities ; Mutation, Missense ; Skin ; Tachycardia

Maxillofacial defect comes from congenital defect, trauma and surgical resection. Patients with intraoral defect are commonly related to maxillary defect and they need prosthetic rehabilitation. Functional reconstruction of partially edentulous mandible has many limitations. However, if both condyles are intact, maxillofacial prosthesis using partial denture give competent results. In this case, a patient of 58 year-old male has a defect on palate and left mandibular posterior teeth from gunshot. The maxillary defect of this patient is Class IV according to Aramany classification and the mandibular one is Type V according to Cantor and Curtis classification. For retention of the obturator, remaining teeth are fully utilized and artificial teeth are arranged harmoniously to provide stable occlusion. Mandibular RPD covered limited range of deformed soft tissue derived from mandibular resection surgery. With these treatments, the patient in this case showed improvements in mastication, swallowing and speech.
Classification ; Congenital Abnormalities ; Deglutition ; Denture, Partial ; Denture, Partial, Removable ; Humans ; Male ; Mandible ; Mastication ; Maxillofacial Prosthesis ; Palate ; Rehabilitation* ; Tooth ; Tooth, Artificial

Binder syndrome is a maxillonasal dysostosis characterized by midface and nasal hypoplasia. It is sometimes associated with short terminal phalanges of fingers and toes and transient radiological features of chondrodysplasia punctata. It is associated with vitamin K deficiency during pregnancy. We describe here a baby with Binder syndrome who was born from mother with cholelithiasis during pregnancy.
Cholelithiasis ; Chondrodysplasia Punctata ; Dysostoses ; Finger Phalanges ; Humans ; Infant ; Maxilla ; Maxillofacial Abnormalities ; Mothers ; Nose ; Pregnancy ; Toes ; Vitamin K ; Vitamin K Deficiency