Browsing by Author "Dayal, J P"
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Item Concomitant occurrence of oral submucous fibrosis, pemphigus and squamous cell carcinoma.(1988-10-01) Dayal, P K; Joshi, H N; Dayal, J PItem Oncocytoma of the parotid gland: report of two cases with comprehensive review of literature.(1984-04-01) Dayal, J P; Saxena, AItem Orofacial manifestations of Sturge-Weber syndrome. Review with a case report.(1991-01-01) Dayal, P K; Shah, S T; Dayal, J PSturge-Weber syndrome is reported in a 19 year old male. Intraoral manifestations of SWS are uncommon. Hence, the present case is reported for the presence of gingival capillary hemangioma which was surgically treated. A review from the literature pertaining to orofacial manifestations of SWS is given.Item A study of the haematologic spectrum of myelodysplastic syndrome.(2001-01-04) Kini, J; Khadilkar, U N; Dayal, J PIn 31 patients of myelodysplastic syndrome, RAEB-t was the commonest subtype (29%), and RARS, the lease common (6.4%); 19.4% were characterised as the unclassifiable (UC) group. Pallor was the dominant sign (90.3%). Low haemoglobin in RA & RARS (p<0.05), thrombocytopenia in RAEB-t (p<0.01) and high leuco/monocyte counts in CMML (p<0.001) were observed. Neutropenia occurred most frequently in RAEB & RAEB-t and circulating blasts in all cases of RAEB-t and CMML. Bicytopenia was the commonest finding (58.1%) and pancytopenia the least (16.1%). 84% of marrows were hypercellular and trilineage dysplasia was seen in 68% of patients. Megaloblastoid dyserythropoiesis was the predominant feature in all cases, dysgranulopoiesis in all cases of RAEB, RAEB-t and CMML, and micromegokaryocytes in all cases of RARS, RAEB & CMML were seen. RAEB-t and RAEB (33.3% each) were the predominant groups which progressed to leukemia, FAB AML-M2, being the commonest type (60%).Item Tuberculosis of the stomach--a case report.(1983-07-01) Dayal, J P; Parikh, B N