Congenital gingival granular cell tumor of newborn.
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Biomedical subjects
Publications and source records attributed to I N Ramdeo.
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Omento-mesentral myxoid hamartoma, a very rare lesion seen in children, is reported in a three year old child. Its rarity, problem in its clinical pre-operative diagnosis, its characteristic gross and microscopic features, its benign, non recurrent clinical course is stressed.
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190 Punjabis (Hindus and Sikhs) of Chandigarh and 152 Hindus of Jodhpur (Rajasthan) were examined for six genetic markers, four of which (APO C-II, C6, C7 and FXIIIA) were not studied before in Asiatic Indians. For APO C-II and C7 only the common phenotype was found in a total of 229 and 99 subjects, respectively. For the remaining four markers the two samples were pooled since the gene frequency estimates were not significantly different: FXIIIA*2 = 0.205 +/- 0.016; C6*B = 0.366 +/- 0.037; PGM1*2 = 0.247 +/- 0.017; PGD*C = 0.041 +/- 0.008. These data may contribute to evaluate the extent of the Mongoloid genetic admixture into the Caucasoid gene pool of the Punjab and Rajasthan Hindu population.
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Serum glycoprotein levels were studied in 50 patients of pulmonary tuberculosis and 25 healthy controls. Ten of the tuberculosis patients had stage I disease, 24 stage II, 9 stage III and 7 had pulmonary tuberculosis with effusion. The serum levels of protein bound hexose, protein bound hexosamine, protein bound fucose and protein bound sialic acid were significantly higher (P less than 0.001) in patients with pulmonary tuberculosis as compared to controls; the mean values being 195.6, 189.1, 16.3 and 120.8 mg/dl respectively in patients and 117.0, 84.1, 7.7 and 67.2 mg/dl respectively in controls. The levels were not influenced by age and sex of the subjects in both groups. The levels were found to increase in all the stages of pulmonary tuberculosis with a marginal difference. Treatment with antituberculosis drugs resulted in a decrease in ESR and the various fractions of serum glycoproteins at subsequent follow up, however, the mean levels did not reach those of control subjects and were not influenced by the type of therapy.
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An uncommon bilateral transitional-type inverted papilloma of the nose and paranasal sinuses is presented, and the salient features of the lesion are discussed. The patient is well and without any signs of recurrence in either side of the nose more than two years after the first diagnosis and complete surgical excision of both tumours. Commonly unilateral, this tumour may occasionally be bilateral. In the present communication an uncommon case of bilateral inverted transitional-type papilloma, with a long history of allergy, is described with some comments on its pathogenesis.