Satya Ranjan Misra

Paget disease of bone: A classic case report.

Paget disease of bone (PDB) is a chronic progressive disease of the bone of uncertain etiology, characterized initially by an increase in bone resorption, followed by a disorganized and excessive formation of bone, leading to pain, fractures, and deformities. It can manifest as a monostotic or polyostotic disease. The prevalence of PDB is common in the Anglo-Saxon population, but relatively rare in India. The disease is often asymptomatic and commonly seen in an aging population. The diagnosis of the disease is mostly based on radiological examination and on biochemical markers of bone turnover. Markedly elevated serum alkaline phosphatase (SAP) is a constant feature while calcium and phosphate levels are typically within normal limits. It is being successfully treated by biphosphonates, a group of anti-resorptive drugs, thereby decreasing the morbidity and mortality associated with the disease. We report a classic case of PDB with craniofacial involvement resulting in Leontiasis Ossea (lion like face), cotton wool appearance of the skull and elevated SAP.

Primary diffuse large B-cell lymphoma in the anterior hard palate: A rare case report with review of literature.

Diffuse large B-cell lymphomas (DLBCLs) are defined as neoplasms of large transformed B cells, i.e. with nuclear diameter more than twice that of a normal lymphocyte. These account for 30-40% of all adult non-Hodgkins lymphomas (NHL). Intraoral lymphomas are relatively rare and often difficult to diagnose in clinical settings. In this case report, we describe a case of primary DLBCL affecting the anterior part of the hard palate of an elderly male patient. DLBCL of anterior part of hard palate is yet to be reported in the English literature, even though DLBCL cases involving the posterior palate have been recorded, thus making the present case to be first of its kind. Emphasis has also been given on the subclassification, differential diagnosis and prognostic antibody factors determining the outcome of DLBCL.

Metastatic hepatocellular carcinoma in the maxilla and mandible, an extremely rare presentation

Malignancy is characterized by anaplasia, invasiveness, and metastasis. Primary oral squamous cell carcinoma is the most prevalent oral malignancy, but secondary malignancy from distant sites have also been reported. Hepatocellular carcinoma (HCC) is a common primary liver malignancy that frequently metastasizes during the course of the disease, but < 1% of cases show oral involvement. Such secondary neoplasms do not have any pathognomonic clinical or radiologic findings, and therefore they pose a diagnostic challenge. Hence, in the differential diagnosis of malignant tumors of the oral cavity, it is essential to consider the occurrence of both primary as well as metastatic tumors despite the low incidence of the latter. A rare case of HCC metastasizing to both the maxilla and mandible is presented, in which the patient succumbed to the disease as a result of the delay in diagnosis.

Calcifying epithelial odontogenic tumor, a rare presentation in children: two case reports.

Calcifying epithelial odontogenic tumor (CEOT) is a rare and benign odontogenic neoplasm that affects the jaws. It is certainly an atypical instance to find this tumor in children. Here, we present two case reports of CEOT presenting in mandible of a 12- and 13-year-old female child, respectively. CEOT have been reported to show features of malignant transformation also.

Papilliferous Keratoameloblastoma: An Extremely Rare Case Report

Odontogenic tumors develop in the jaw bones from the odontogenic tissue-oral epithelium in tooth germ, enamel organ, dental papilla, reduced enamel epithelium, remnants of Hertwigs root sheath or dental lamina, and so forth. Hence, a bewildering variety of tumors are encountered in the maxilla and mandible. Ameloblastoma is the second most common odontogenic neoplasm after odontomes, and it has numerous clinical and histologic variants. We report a very rare histologic variant: the papilliferous keratoameloblastoma which is the fifth reported case in the English literature.

A bibliometric analysis of two PubMed-indexed high-impact factor endodontic journals: A comparison of India with other countries

Aim: The present study was conducted with an aim to determine the number and trends of published articles in the International Endodontic Journal (IEJ) and Journal of Endodontics (JOE) from 2009 to 2014. Settings and Designs: A retrospective observational study was conducted for IEJ and JOE. Subjects and Methods: All issues of IEJ and JOE were electronically and hand searched for the following parameters: Amount of papers, publication year, affiliated organizations, and countries. Statistical Analysis Used: The data were organized and analyzed using software SPSS version 21.0; descriptive statistics was used. Results: A total of 872 articles were analyzed in the IEJ and JOE with 1606 papers. Brazil had the largest number of articles (170) mainly in IEJ, and the USA (350) in JOE. Indians published more of their research in JOE than IEJ. Conclusions: Original articles in endodontic publication from different universities in India have considerably increased, showing that research is becoming more important.

Recurrent osteomyelitis of the mandible in osteopetrosis: a common complication of an uncommon disease

Osteopetrosis is a congenital disease characterised by overtly dense bone with obliteration of marrow spaces, owing to defective osteoclast function, resulting in excessive and defective bone formation. It is rare, having an incidence of 1 in 250 000 births.1 Diffuse generalised osteosclerosis of bones is seen and serious oral complications such as osteomyelitis with exposed necrotic bone may occur in the jaws.2 Ten per cent of osteopetrosis cases develop osteomyelitis that usually involves the mandible. Osteomyelitis of the maxilla is very rare, probably because of the thin cortical bone and rich collateral blood supply. Osteopetrotic bones lack a bone marrow cavity, fail to resist normal physical loads, and are vulnerable for fractures due to lack of remodelling.1 Osteopetrosis is generally diagnosed through skeletal radiographs in which there is increased radiodensity and hence the name ‘Marble bone disease’.3 Dentists should be aware of the disease because tooth extraction in such patients results …

Nasoalveolar cyst: an enigma for the dentist

A nasoalveolar cyst is a rare, non-odontogenic soft tissue cyst encountered in the anterior maxillary labial sulcus as an asymptomatic soft tissue swelling. Often, patients with these cysts report them to the dental clinic where they are mistaken for odontogenic lesions by the dental surgeon, especially if concomitant dental problems are present. They cannot be detected by routine conventional dental radiography as they are peripheral, lying within the mucosa thereby posing a diagnostic challenge. We document a case of a 47-year-old woman with a nasoalveolar cyst.

Diagnostic procedures for autoimmune vesiculobullous diseases: A review

Oral soft tissues are affected by numerous pathologic conditions of variable etiology and hence their appropriate management relies on their accurate diagnosis. Clinical identification of intact vesicle and bulla in the oral cavity is really a challenge due to the regular irritation and the friable nature of oral mucosa. Rupture of these lesions leads to erosions or ulcerations on the surface, hence making the diagnosis of vesiculobullous (VB) lesions is even more difficult due to the fact that the differential diagnosis along with VB lesions will also include ulcerative, immunological-mediated diseases, and neoplasms and systemic diseases. Hence, knowledge of the clinical presentation of these disorders and the relevant diagnostic procedures is important not just for dermatologists, but also for general practitioners and dentists. In this article, the various procedures have been explained that can be used for the diagnostic purpose of VB lesions.

Cherubism with multiple dental abnormalities: a rare presentation

Cherubism is a progressive, hereditary fibro-osseous lesion exclusively affecting the jaw bones. It is caused by the abnormal functioning of osteoblasts and osteoclasts, leading to replacement of normal bone by cellular fibrous tissue and immature bone, which produces painless progressive growth of the jaw, with a round facial appearance. It was first described in 1933 by Jones as ‘familial multilocular cystic disease of the jaws’. The term ‘cherubism’ was later coined to describe the rounded facial appearance resulting from jaw hypertrophy that was reminiscent of cherubs depicted throughout Renaissance art. The bony lesions generally occur at an early age, affect one or both jaws symmetrically, and grow progressively until puberty. Spontaneous regression is seen in most cases, although surgical re-contouring may be required for others for aesthetic reasons.