Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Jaydeep N. Pol"'
Autor:
Jaydeep N. Pol, Sayali Deshmukh, Anand Bhosale, Priya Hombalkar, Vivek Dugad, Pallavi S. Chaudhari, Rajan S. Bindu, Praneet Awake, Sneha Patrike
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 17, Iss 4, Pp 793-797 (2024)
Context: Testicular regression syndrome (TRS), clinically termed “vanishing testes,” is a condition with atrophy of testes in late fetal or early neonatal life. The spermatic cord ends blindly or into a small fibrovascular nubbin. Histopathology
Externí odkaz:
https://doaj.org/article/6160e3b0da61415d8f74cc29bee65187
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 Oncology. 9:279-281
Osseous choristoma is the formation of normal mature bone at an abnormal position. These are rare benign tumor-like growth usually asymptomatic except growth or swelling as the clinical presentation. In oral cavity, osseous choristoma is rare and com
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
Publikováno v:
IP Archives of Cytology and Histopathology Research. 6:283-287
Chromophobe Renal Cell Carcinoma (ChRCC) is a rare distinct subtype of Renal cell carcinoma. It arises from intercalated cells of the renal cortex. The cytomorphological features of ChRCC show significant overlap with Clear cell Renal Cell Carcinoma