Biomedical subjects
Publications and source records attributed to P K Dayal.
Apert syndrome is a rare congenital anomaly characterized by acrocephaly, syndactyly, and abnormalities of other organs. It has characteristic features in the orofacial region, affecting the eyes, palate, middle third of face, and uvula. In this case report, the features of Apert syndrome, particularly in relation to the orofacial region, are discussed.
Primary intraosseous carcinoma (PIOC) of the jaws is a rare lesion and majority of them arise from the epithelial lining of pre-existing odontogenic cysts (OCS). In a case of 20 year old male, PIOC presented a painless swelling extending from left posterior side of the mandible to across the midline with a duration of three months. X-rays revealed a cystic Unilocular radiolucency with well demarcated margin. Aspiration revealed the characteristics of cystic fluid. Histological examination of the biopsy specimen following marsupialisation showed SCA arising in cystic lining. In another case of 24 year old female, PIOC presented a painless swelling on the right side of the mandible with a hollow cavity seen intraorally in the region of the first molar, exfoliated itself in one month. X-rays revealed a cystic radiolucency but with irregular margin centrally. Histologic examination of a biopsy specimen from the lining of the cavity showed SCA originating in cystic lining. In both cases habit of tobacco was absent.
Hyalinosis cutis et mucosae (lipoid proteinosis) is a rare disorder characterized by hyaline and lipid deposits in the skin and mucous membrane of the oral cavity, upper respiratory tract, and internal organs. It usually appears in infancy with hoarseness. This disorder is particularly interesting because of its rarity and wide range of clinical manifestations. We report a case that demonstrated manifestations of lipoid proteinosis.
The case of a 30-year-old man with aglossia is reported. Aglossia, a rare condition, is a developmental disorder in which the entire tongue is absent. It is usually associated with jaw and facial anomalies. In this patient, both the maxilla and mandible were affected. Although the mortality rate of patients with aglossia is high, this patient has been able to cope with his oral function with minimal obstruction.
Cheilitis glandularis is reported in two farmers with characteristic clinical and histopathological features. Both patients were treated with vermilionectomy. The prognosis was good.
Sera from 47 healthy controls, 18 normal individuals with the habit of tobacco chewing, 43 patients with oral precancerous (PC) conditions, and 40 patients with oral cancer (OC) were studied for the levels of total sialic acid (TSA), lipid-bound sialic acid (LSA), mucoid proteins, and protein-bound hexoses (PBH) (galactose and mannose). The changes in the glycoconjugate levels were insignificant between the controls and the normal tobacco chewers. All four parameters were significantly elevated in oral PC patients compared with controls. The levels of PBH and LSA showed significant increase in the oral PC patients compared with the normal tobacco chewers. A significant increase was observed in the levels of TSA, LSA, mucoid proteins, and PBH in OC patients compared with controls, normal tobacco chewers, and patients with oral PC. Increasing levels of all the biomarkers were found with progression of the malignant disease. Elevations in the levels of TSA and LSA were statistically significant in Stage IV patients compared with Stage III patients. The patients with metastases had higher levels of the biomarkers than the patients with primary OC. However, elevations only in LSA levels were statistically significant. These results suggest that evaluations of the serum glycoconjugate levels may be useful in diagnosis of the patients with oral PC or OC. In addition to their value in early detection, they can also help in staging of the disease.
A rare Aarskog syndrome is reported in a 12-year-old boy. The patient had a triad of characteristic symptoms consisting of short stature, genital anomaly, and unusual facies. Both jaws were hypoplastic with presence of crowded permanent teeth and over-retained deciduous teeth. Radiographic examination of teeth showed taurodontism, which has not been reported previously.
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