Nibedita Sahoo

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Alteration in glutamine synthetase activity was studied in excisedsenescing leaves of rice (Oryza sativa L.) of asalt-sensitive (Ratna) and a salt-tolerant (Getu) cultivar subjected toNaCl-stress. Glutamine synthetase activity declined during senescence indarkness, but increased initially and then decreased under light treatment,which is correlated with the(More)
Ovarian fibromas are benign sex cord stromal tumours occurring in peri-menopausal and post-menopausal women. These tumours are composed of spindle fibroblastic cells producing collagen. They are almost always endocrine-inert and are rarely associated with hormone production. We report herein a case of a 60-year-old Indian woman presenting as post-menopausal(More)
TO THE EDITOR: We read with interest the recent paper by Francis et al outlining a morphological classification of vitreous seeds in retinoblastoma and their response to intravitreal melphalan. The authors have ably provided a means of prognostication while dealing with a component of the disease that has always been notoriously difficult to treat.(More)
Filariasis is a global social health problem of tropical and sub tropical countries like India. W.bancrofti accounts for 95% of cases of lymphatic filariasis. Microfilaria in cytosmears are a rare finding. We report a case of 55 year old female presented with right axillary swelling with ipsilateral breast lump. Cytosmears from the lymph node aspirate(More)
Handful cases of invasive Cystic Hypersecretory Ductal Carcinoma (CHC) have been reported so far in literature. Cystic hypersecretory lesions of breast have a spectrum of morphological features ranging from Cystic Hypersecretory Hyperplasia (CHH), CHH with atypia, in situ to invasive CHC. We are reporting a case of a 32-year-old female who had nipple(More)
Phyllodes tumors are uncommon fibroepithelial neoplasms of breast. Heterologous sarcomatous differentiation of malignant phyllodes tumor (MPT) is a rare phenomenon as shown in the literature. Herein we report a series of nine cases from a tertiary care centre in Eastern India. Patients demographic data and clinical details were obtained from the medical(More)
The causal relationship of autosomal dominant polycystic kidney disease (ADPKD) with the development of renal cell carcinoma (RCC) is still not known. We describe a case of bilateral PKD complicated with a large enhancing mass and multiple small nodules in the left kidney. The histopathological study of the nephrectomy specimen revealed the synchronous(More)