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Metanephric adenoma (MA) is a rare, benign tumour of the kidney, that can have a microscopic appearance similar to a nephroblastoma (Wilms tumours), [1] or a papillary renal cell carcinoma. It should not be confused with the pathologically unrelated, yet similar sounding, mesonephric adenoma .
INASP initiated BanglaJOL in June 2007 and officially launched it in September 2007. [2] The Bangladesh Academy of Sciences assumed management of BanglaJOL in 2014. [3]It is a database of open access journals published in Bangladesh, dealing with the full range of academic disciplines including both paper based and online only publications.
Nephrogenic adenoma is a benign growth typically found in the urinary bladder. It is thought to result from displacement and implantation of renal tubular cells, as this entity in kidney transplant recipients has been shown to be kidney donor derived. [1] This entity should not be confused with the similar-sounding metanephric adenoma.
Here, first a fertilised egg implants into the uterus, but some cells around the fetus (the chorionic villi) do not develop properly. The pregnancy is not viable, and the normal pregnancy process turns into a benign tumour. There are two subtypes of hydatidiform mole: complete hydatidiform mole, and partial hydatidiform mole. [citation needed]
Rhabdoid tumors have a distinctive histology and abnormalities (i.e. loss of heterozygosity, single nucleotide polymorphism, and deletions) in chromosome 22. [11] Clear cell sarcoma of the kidney, which is responsible for 5-10% of childhood pediatric tumors, occurs predominantly in children from 2 to 3 years of age. Unlike mesoblastic nephroma ...
Diagram shows the sequential development and degeneration of the pronephros and mesonephros, and the induction of the ureteric bud and metanephric mesenchyme during kidney development in mammals. The development of the kidney proceeds through a series of successive phases, each marked by the development of a more advanced kidney: the ...
Metanephric dysplastic hematoma of the sacral region (MDHSR) has been described by Cozzutto and Lazzaroni-Fossati in 1980, [1] by Posalaki et al. in 1981 [2] and by Cozzutto et al. in 1982. [3] Three additional cases were seen by Finegold.
Thus, the life of a fetus in fetu is akin to that of a tumor in that its cells remain viable by way of normal metabolic activity. However, without the gestational conditions in utero with the amnion and placenta , a fetus in fetu can develop into, at best, an especially well differentiated teratoma ; or, at worst, a high-grade metastatic ...