Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Jaydeep N Pol"'
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 67, Iss 1, Pp 178-181 (2024)
Xp11 translocation renal cell carcinoma (XPTRCC) is a very rare kidney neoplasm, which has been predominantly reported in young patients. Sarcomatoid transformation in renal cell carcinomas is known. However, its occurrence in XPTRCC is unreported so
Externí odkaz:
https://doaj.org/article/19510bdb28fd45a1aeea593a3756d128
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 66, Iss 4, Pp 819-822 (2023)
Solitary fibrous tumor (SFT) is a rare mesenchymal tumor of fibroblastic origin commonly occurring in pleura. It can occur at many extrapleural sites but is rare in orbit. Most cases are benign and recurrence is not unusual in the head and neck and o
Externí odkaz:
https://doaj.org/article/31463ffbf4174045812fd891b04168c9
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 16, Iss 2, Pp 290-293 (2023)
Neurenteric cysts are rare congenital abnormalities, commonly occurring in the spinal region, composed of heterotopic endodermal tissue components. We present a case of six months child having cough and intermittent fever. Computed tomography scan sh
Externí odkaz:
https://doaj.org/article/50ba709f9b3341cf86648b80a096c2bf
Autor:
Rakhi V Jagdale, Jaydeep N Pol
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 64, Iss 2, Pp 343-346 (2021)
Background: Renal oncocytomas are benign epithelial tumors usually detected incidentally. They are typically solid,well-circumscribed,homogenous,mahoganybrown with a central stellate scar.Sometimes,they can have cystic degenerationand rarely present
Externí odkaz:
https://doaj.org/article/da8cf641579945058638c0862e315f88
Autor:
Rakhi V Jagdale, Jaydeep N Pol
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 63, Iss 4, Pp 623-626 (2020)
Rhabdomyosarcoma (RMS) masquerading as acute leukemia (AL) is very rare. We report a case which presented as acute leukemia subsequently diagnosed to be Alveolar RMS of Urinary Bladder. Although cases of RMS with leukemic presentation have been repor
Externí odkaz:
https://doaj.org/article/0567b64f947e4eecaa1506ee2926dffd
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 63, Iss 5, Pp 134-140 (2020)
Aims: To explore clinical, histopathological and immunohistochemistry (IHC) features of mammary analogue secretory carcinoma (MASC) with systematic literature review. Settings and Design: Hospital based cross-sectional study. Subjects and Methods: Th
Externí odkaz:
https://doaj.org/article/9e59542353cd4a86aa938db7995b8b11
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 2, Pp 306-309 (2019)
Primary tumors of the paratesticular region are rare, with sarcomas constituting a major proportion, particularly in the old age. The paratesticular region consists of mesothelial, various epithelial, and mesenchymal cells and may therefore give rise
Externí odkaz:
https://doaj.org/article/2ff0375fe20942428242734dcfb20081
Publikováno v:
Journal of the Scientific Society, Vol 44, Iss 2, Pp 106-109 (2017)
Primary peritoneal serous adenocarcinoma (PPSA) is a rare primary peritoneal tumor in women. Ovarian, tubal, and peritoneal serous carcinomas have similar pathologic findings. CA125 is the common biomarker used for diagnosis, monitoring treatment res
Externí odkaz:
https://doaj.org/article/56e58a41be3e44bd806568e2516f5c5c
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 60, Iss 1, Pp 139-140 (2017)
Externí odkaz:
https://doaj.org/article/98868a42684b42ceaa478c7a2ac663fc
Publikováno v:
IP Journal of Diagnostic Pathology and Oncology. 7:6-12
Epithelioid sarcoma (ES) is a malignant mesenchymal neoplasm that exhibits epithelioid cytomorphology and a predominantly epithelial phenotype. The principal types based on histopathological features and location; include the classic or conventional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dc0733e83445aff9d1ad2896ae1c147
https://doi.org/10.18231/j.jdpo.2022.002
https://doi.org/10.18231/j.jdpo.2022.002