Central Giant Cell Granuloma.

World Health Organization (WHO) defines central giant cell granuloma (CGCG) as an intraosseous lesion consisting of cellular fibrous tissue and contains many foci of hemorrhage, aggregations of multinucleated giant cells, and occasionally trabeculae of woven bone. Clinically and histopathologically CGCG resembles many other jaw lesions hence it has to be differentiated from them for judicious management of the lesion. Here we present a case of CGCG of palate in a 21-year-old female patient.[Jigna SNJIRM 2016; 7(5):101-104]

Sweet’s syndrome.

Acute febrile neutrophilic dermatosis or Sweet’s syndrome (SS) is characterized by painful, erythematous plaques of rapid onset accompanied by fever. The etiology of SS is unknown and it may be associated with antecedent infections, malignancies, autoimmune diseases, drugs and vaccines, upper respiratory or gastrointestinal infection, pregnancy, inflammatory bowel disease as well as chemotherapy or idiopathic. The standard therapy for SS is systemic corticosteroids. We report a rare case of 19‑year‑old young male patient with complaint of severe ill‑defined type of pain in both jaws associated with plaques and papules on extensor surfaces of upper and lower extremities with bodyache and myalgia. Histopathological examination suggested perivascular neutrophilic infiltration with scattered eosinophils. Sweet syndrome has rare oral manifestations secondary to hematological changes. It can also present as a paraneoplastic syndrome (malignancy‑associated form of condition, which is most commonly related to acute myelogenous leukemia), which leads to poor prognosis and thus it requires careful examination, early diagnosis and long‑term follow‑up.

Adenoid cystic carcinoma arising from minor salivary glands of palate involving maxillary sinus.

Adenoid cystic carcinoma (ACC) was first described by Billroth in 1856 and was called ‘cylindroma’ due to its characteristic histological appearance. ACC is the most common malignant neoplasm of the lacrimal gland, and the second most common type of carcinoma arising in the salivary glands, following mucoepidermoid carcinoma. Palate is the most commonly affected site followed by parotid gland, submandibular gland, antrum & tongue. Characteristic features include aggressive, slow growth, with insidious destruction of surrounding tissues, perineural invasion, prolonged clinical course and the tendency for delayed onset of the distant metastases which worsens the prognosis. Long term survival can be achieved particularly with combined surgery and radiotherapy. The most common pattern is the cribriform architecture. Histopathology is the gold standard for the diagnosis of ACC. CT & MRI are considered to be of almost similar significance in detection of perineural spread with preference to MRI because of its high soft tissue contrast. Here we have mentioned a case of Adenoid Cystic carcinoma arising from minor salivary glands of palate.

Multidisciplinary Approach for an Initially Misdiagnosed Case of Osteosarcoma in a Medically Compromised Patient.

Osteosarcoma is a highly malignant bone tumour. It is derived from primitive mesenchymal bone forming cell. Osteosarcoma of the jaw is quite rare. Despite its rarity, the dentist may be the first health professional who observes tumours involving the jaws. As there is a greater variability in clinical, radiological and histopathological findings of jaw osteosarcoma, so there is greater scope for multidisciplinary approach. An early definite diagnosis is must for successful treatment which can save patient’s life and esthetic. This article presents a case of osteosarcoma in medically compromised 17 years old female patient who was misdiagnosed initially and later on present as a huge size of the tumour mass with gross disfigurement than she was treated by multidisciplinary approach of oncosurgeon, medical oncologist and radiation oncologist with appropriate expertise.

Papillon-Lefevre syndrome: two case reports.

Papillon-Lefevre syndrome is a rare autosomal recessive disorder in which there is palmoplantar keratinization and premature loss of both deciduous and permanent teeth. The palmoplantar keratoderma typically has its onset between the ages of 1 and 4 years and severe periodontitis starts at the age of 3 or 4 years. An early diagnosis of the syndrome can help preserve the teeth by early institution of treatment, using a multidisciplinary approach. We present two cases of the syndrome having all of the characteristic features.