Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Richa Bhartiya"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 8, Pp ED09-ED11 (2016)
Hairy cell leukemia is a chronic lympho-proliferative disease. It is indolent but progressive in nature. It arises from B-cell lineage. We report an incidentally detected case of Hairy Cell Leukaemia (HCL) in a 55-year-old male patient with Herpes s
Externí odkaz:
https://doaj.org/article/80c2595a31ad45ad83fdad73b5765828
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 5, Pp ED10-ED11 (2016)
The ovarian lymphoma is rare. Lymphoma presenting as an ovarian mass with initial manifestation is even rarer. We report a case of primary Non-Hodgkin’s Lymphoma (NHL) of left ovary in a 52-year-old female presented with distension of abdomen and
Externí odkaz:
https://doaj.org/article/e45c2ff1735a452ea09fbc01026c0c2b
Autor:
Richa Bhartiya, K M Prasad
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 12, Pp ED21-ED22 (2015)
Malignant Melanoma of nasal cavity is an extremely rare tumour and is more aggressive than its cutaneous counterpart. Primary malignant melanoma of nasal cavity arise from melanocytes located in the mucous membrane. Only 0.5% of malignant melanoma a
Externí odkaz:
https://doaj.org/article/279e12974c7c4f0cb8fb379f0ddd9deb
Publikováno v:
Annals of Pathology and Laboratory Medicine. 5:C85-90
Hodgkin’s lymphoma (HL) is one of the curable diseases in pregnancy. Since pregnant females are immuno-compromised, so it is important to know about the course and progression of this common entity in pregnancy. Fine needle aspiration cytology is m
Publikováno v:
Indian Journal of Pathology and Oncology. 6:714-716
Amyloidosis is a rare systemic disease characterised by deposition of misfolded aberrant precursor protein, which forms fibrils in beta-pleated sheets. Waldenstrom’s macroglobulinemiais one of the uncommon causes of systemic amyloidosis. Diagnosis
Publikováno v:
Annals of Pathology and Laboratory Medicine. 4:C102-C105
Background: Rhinosporidiosis is a chronic granulomatous disease caused by Rhinosporidium seeberi. It is endemic in India & Sri Lanka. It usually involves the nasal cavity & rarely other sites including skin. Cutaneous rhinosporidiosis presents as pap
Publikováno v:
Indian Journal of Medical and Paediatric Oncology : Official Journal of Indian Society of Medical & Paediatric Oncology
Background: Fine-needle aspiration (FNA) of the thyroid gland has proven to be an important and widely accepted, cost-effective, simple, safe, and accurate method triaging patients with thyroid nodules. Awareness and understanding of wide spectrum th
Publikováno v:
Annals of Pathology and Laboratory Medicine. 4:C131-C133
Melorheostosis is a rare, benign, and disabling condition . It is a rare mesenchymal bone disease classified as a sclerotic bone dysplasia. We present this case because of its rarity and highlight the importance of Fine needle aspiration cytology whi
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 8, Pp ED09-ED11 (2016)
Hairy cell leukemia is a chronic lympho-proliferative disease. It is indolent but progressive in nature. It arises from B-cell lineage. We report an incidentally detected case of Hairy Cell Leukaemia (HCL) in a 55-year-old male patient with Herpes si
Autor:
K M Prasad, Richa Bhartiya
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 12, Pp ED21-ED22 (2015)
Malignant Melanoma of nasal cavity is an extremely rare tumour and is more aggressive than its cutaneous counterpart. Primary malignant melanoma of nasal cavity arise from melanocytes located in the mucous membrane. Only 0.5% of malignant melanoma ar