Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Parikshit Padhi"'
Publikováno v:
Current Problems in Cancer: Case Reports, Vol 13, Iss , Pp 100279- (2024)
Renal angiosarcomas are rare malignancies with approximately 70 published cases and comprise less than 1 % of all kidney tumors. We present an elderly male who was found to have a large 10 cm kidney mass and underwent a left radical nephrectomy. Path
Externí odkaz:
https://doaj.org/article/3fcf005ad11b4cafb92cd6b19d220855
Autor:
Parikshit Padhi, Naga Praneeth Raja
Publikováno v:
Current Problems in Cancer: Case Reports, Vol 11, Iss , Pp 100257- (2023)
Externí odkaz:
https://doaj.org/article/32fe51bc8bf4407a820941ee1f231ff8
Autor:
Parikshit Padhi
Publikováno v:
Current Problems in Cancer: Case Reports, Vol 9, Iss , Pp 100225- (2023)
Externí odkaz:
https://doaj.org/article/920706229ff14437acb68ac0e6b9c7ef
Autor:
Parikshit Padhi, Margarita Topalovski
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2021 (2021)
Benign metastasizing leiomyoma (BML) is a rare spindle cell neoplasm seen in middle-aged women who have a history of leiomyoma of the uterus. The most common sites of metastases are the lungs; however, other sites of spread have been documented. Thes
Externí odkaz:
https://doaj.org/article/bfd634817c654dd5adc20f02e487bd45
Autor:
Parikshit Padhi, Radwa El-Behery
Publikováno v:
Case Reports in Hematology, Vol 2020 (2020)
Extramedullary plasmacytomas (ESPs) are rare forms of plasma cell dyscrasias and usually are seen in the upper aerodigestive tract. ESPs with anaplastic features are extremely rare, and no treatment guidelines exist. We present a 75-year-old gentlema
Externí odkaz:
https://doaj.org/article/141757503b32404b89a5497226d7b742
Autor:
Parikshit Padhi, Margarita Topalovski, Radwa El Behery, Eduardo S. Cantu, Ramadevi Medavarapu
Publikováno v:
Case Reports in Oncological Medicine, Vol 2018 (2018)
Chronic Myelogenous Leukemia in blast crisis can manifest as either myeloid (more common) or lymphoid blast crisis. Most lymphoblastic crises are of B-cell lineage. T-cell blast crisis is extremely rare, with only a few reported cases. We present a c
Externí odkaz:
https://doaj.org/article/50161695414b4c1eabf69f8a85ca99a3
Autor:
Margarita Topalovski, Parikshit Padhi
Publikováno v:
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology, Vol 2021 (2021)
Case Reports in Obstetrics and Gynecology, Vol 2021 (2021)
Benign metastasizing leiomyoma (BML) is a rare spindle cell neoplasm seen in middle-aged women who have a history of leiomyoma of the uterus. The most common sites of metastases are the lungs; however, other sites of spread have been documented. Thes
Publikováno v:
Journal of Onco-Nephrology. 4:37-40
Chronic graft-versus-host disease is a potentially life-threatening immunological complication which can occur any time after hematopoietic stem cell transplant. Many organ systems can be affected; however, kidneys are normally not and development of
Publikováno v:
Clinical Therapeutics. 39:2146-2157
Purpose Neuroendocrine tumors (NETs) are heterogeneous tumors that arise from the neuroendocrine cells of the digestive tract and other organs, such as the lung, ovary, and thyroid glands. They can be well differentiated or poorly differentiated, and
Publikováno v:
Case Reports in Oncological Medicine
Case Reports in Oncological Medicine, Vol 2018 (2018)
Case Reports in Oncological Medicine, Vol 2018 (2018)
Chronic Myelogenous Leukemia in blast crisis can manifest as either myeloid (more common) or lymphoid blast crisis. Most lymphoblastic crises are of B-cell lineage. T-cell blast crisis is extremely rare, with only a few reported cases. We present a c