Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Nasma K Majeed"'
Publikováno v:
SAGE Open Medical Case Reports, Vol 8 (2020)
Peliosis hepatis is a rare condition characterized by blackish-blue blood-filled cavities in hepatic parenchyma caused by dilatation of hepatic sinusoids. Peliosis hepatis has been described in secondary immunodeficiencies and certain medications. We
Externí odkaz:
https://doaj.org/article/9904711d91fe44cc924d0489cc70738d
Publikováno v:
Clinical Pathology, Vol 12 (2019)
Sarcomatoid renal cell carcinoma is an uncommon and aggressive renal tumor with rapid disease progression. A median survival time is only 4-9 months after diagnosis. Osteogenic differentiation is a rare feature of the tumor. Here, we present a case o
Externí odkaz:
https://doaj.org/article/b9d3df6d92af4c85a974740a58a189c2
Autor:
Alaa Alsadi, Nasma K. Majeed, Dereen M. Saeed, Yash Dharmamer, Manmeet B. Singh, Tushar N. Patel
Publikováno v:
Journal of Nephropathology, Vol 11, Iss 3, Pp e17123-e17123 (2022)
Introduction: Identification of electron-dense immune deposits in electron microscopy (EM) images is integral to the diagnosis of medical renal disease. Deep learning has the potential to augment this process, especially in areas with limited resourc
Externí odkaz:
https://doaj.org/article/6daac2e846fd4a2a81404d5e0822af59
Publikováno v:
Case Reports in Pathology, Vol 2020 (2020)
Angiosarcoma is a high-grade vascular tumor arising from endothelial cells of blood vessels. It represents less than 1% of the mesenchymal tumors. Uterine angiosarcoma is an extremely rare tumor with less than 25 cases reported in the literature. It
Externí odkaz:
https://doaj.org/article/8e80d55e5f2d4999ba40b7d71436d112
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 6 (2019)
Rationale: Lipoprotein glomerulopathy (LPG) is a rare renal disorder that features glomerular capillary lipoprotein thrombi, proteinuria, and progressive renal failure. Although most reported cases describe involvement in Asian patients, occurrence i
Externí odkaz:
https://doaj.org/article/0e5c40d845f44ce4a779e153d222cd5c
Autor:
Dereen Mohammed Saeed, Ismail Elbaz Younes, Redouane Boumendjel, Nasma K Majeed, David Hakimian
Publikováno v:
Comparative Clinical Pathology. 29:1087-1090
Myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis (MDS/MPN with RS-T), which exhibits both an increased number of marrow ring sideroblasts and thrombocytosis, is a rare disorder classified as one of the newly estab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9532ab091bf6bcefe9e6aa971ded4863
https://doi.org/10.1007/s00580-020-03149-1
https://doi.org/10.1007/s00580-020-03149-1
Publikováno v:
JCO Oncology Practice. 16:608-610
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cbaac04c80796c2246f975a5eba821a
https://doi.org/10.1200/op.20.00008
https://doi.org/10.1200/op.20.00008
Publikováno v:
SAGE Open Medical Case Reports, Vol 8 (2020)
SAGE Open Medical Case Reports
SAGE Open Medical Case Reports
Peliosis hepatis is a rare condition characterized by blackish-blue blood-filled cavities in hepatic parenchyma caused by dilatation of hepatic sinusoids. Peliosis hepatis has been described in secondary immunodeficiencies and certain medications. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4fa530905e17ff3b751208b46779393
https://doaj.org/article/9904711d91fe44cc924d0489cc70738d
https://doaj.org/article/9904711d91fe44cc924d0489cc70738d
Publikováno v:
Case Reports in Pathology
Case Reports in Pathology, Vol 2020 (2020)
Case Reports in Pathology, Vol 2020 (2020)
Angiosarcoma is a high-grade vascular tumor arising from endothelial cells of blood vessels. It represents less than 1% of the mesenchymal tumors. Uterine angiosarcoma is an extremely rare tumor with less than 25 cases reported in the literature. It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc0322c17099cbdda8fb460ae3262ee3
http://europepmc.org/articles/PMC7060455
http://europepmc.org/articles/PMC7060455
Autor:
Yasser R. Farid, Nasma K Majeed, Benjamin E. Onderdonk, Grace Guzman, Christina H. Son, Philip P. Connell, David M. Rosenberg
Publikováno v:
JBJS case connector. 9(4)
CASE Heterotopic ossification (HO) is a pathological formation of bone in nonosseous tissue and is a common complication of orthopaedic procedures. Radiotherapy is often used to prevent HO despite the small risk of secondary malignancy. Here, we repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b538f9abb36c447a87c710bb5e6bc90
https://pubmed.ncbi.nlm.nih.gov/31815809
https://pubmed.ncbi.nlm.nih.gov/31815809