Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Prabir, Chandra Paul"'
Publikováno v:
Journal of Forensic Science and Medicine, Vol 10, Iss 1, Pp 28-33 (2024)
Background and Objectives: The cases of apparent natural deaths are encountered in the hospital casualties who are noted dead at the time of the first medical attention and as such are labeled as ”Brought Dead.” These include the cases of sudden
Externí odkaz:
https://doaj.org/article/135fa49c50d34da3819503408c417dba
Autor:
Soumit Dey, Saikat Datta, Snehamay Chaudhuri, Prabir Chandra Paul, Binny Khandakar, Sonali Mandal
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 3, Pp EC16-EC19 (2016)
Introduction: The deep seated ovarian lesions unapproachable by unguided aspiration cytology were easily done under ultrasound guidance. It gave a before hand cytological diagnosis of the lesion to the surgeon determining the modality of treatmen
Externí odkaz:
https://doaj.org/article/086b5e5e23fd4faa8a23eab4ab400d11
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 12, Pp ED19-ED20 (2015)
Giant cell tumour of soft tissue is an extremely rare tumour. It is thought to be the soft tissue counterpart of giant cell tumours of the bone due to its histological and immunohistochemical resemblances. Almost 80% of these tumours occur in upper
Externí odkaz:
https://doaj.org/article/449b85c18a2c48ff8797bd76c61540ec
Testicular fibroma of gonadal stromal origin with minor sex cord elements, presenting with hydrocele
Autor:
Saikat Datta, Soumit Dey, Sumana Mukherjee, Prabir Chandra Paul, Aparna Bhattacharyya, Sukdeb Biswas, Balaram Tudu
Publikováno v:
Rare Tumors, Vol 5, Iss 3, Pp e34-e34 (2013)
Testicular fibroma of gonadal stromal origin is a rare benign tumor of testis which usually presents as a slow growing testicular mass. Only 25 cases of testicular fibroma have been reported in the literature. Presence of minor sex cord elements in t
Externí odkaz:
https://doaj.org/article/b29a3a0103e944d6bc0eaa31eaa62ffb
Autor:
Prabir Chandra Paul, Soumit Dey, Snehamay Chaudhuri, Binny Khandakar, Sonali Mandal, Saikat Datta
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 3, Pp EC16-EC19 (2016)
Introduction: The deep seated ovarian lesions unapproachable by unguided aspiration cytology were easily done under ultrasound guidance. It gave a before hand cytological diagnosis of the lesion to the surgeon determining the modality of treatment fo
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 12, Pp ED19-ED20 (2015)
Giant cell tumour of soft tissue is an extremely rare tumour. It is thought to be the soft tissue counterpart of giant cell tumours of the bone due to its histological and immunohistochemical resemblances. Almost 80% of these tumours occur in upper a
Publikováno v:
Archives of Iranian medicine. 17(10)
Primary renal synovial sarcoma (PRSS) is a very rare tumor, first described by Argani, et al. The exact incidence of PRSS is not yet known. Here we present a case of PRSS diagnosed by histopathology, supplemented with immunohistochemistry.
Clinicohaematological profile of aplastic anaemia in a rural medical college of Northern West Bengal
Autor:
Sudipta, Chakrabarti, Bidyut Krishna, Goswami, Prabir Chandra, Paul, Supriya, Sarkar, Srikrishna, Mondal, Shikha, Das
Publikováno v:
Journal of the Indian Medical Association. 111(10)
There is a scarcity of clinical data in the field of aplastic anaemia from rural India. Present study was conducted in North Bengal Medical College to find out the clinicohaematological profile and the possible aetiological factors in patients with a
Publikováno v:
Journal of Pediatric Ophthalmology & Strabismus. 47:1-3
Retinal dysplasia is a rare non-neoplastic congenital disorder characterized by aberrant differentiation of the retina with formation of abnormal tubular and rosette-like structure. Clinically, the lesion presents with leukocoria and mimics a retinob
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 52, Iss 2, Pp 231-233 (2009)
Extraovarian granulosa cell tumor (GCT) is a very uncommon tumor, assumed to arise from the ectopic gonadal tissue along the embryonal route of the genital ridge. One such rare case of extraovarian GCT was encountered in a 58-year-old female who pres