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Description
  • Juxtaglomerular cell tumor (JGCT) generally affects adolescents and young adults. The patients experience symptoms related to hypertension and hypokalemia due to renin-secretion by the tumor. Grossly, the tumor is well circumscribed with fibrous capsule and the cut surface shows yellow or gray-tan color with frequent hemorrhage. Histologically, the tumor is composed of monotonous polygonal cells with entrapped normal tubules. Immunohistochemically, tumor cells exhibit a positive reactivity for renin, vimentin and CD34. Ultrastructurally, neoplastic cells contain rhomboid-shaped renin protogranules. Genetically, losses of chromosomes 9 and 11 were frequently observed. Clinically, the majority of tumors showed a benign course, but rare tumors with vascular invasion or metastasis were reported. JGCT is a curable cause of hypertensive disease if it is discovered early and surgically removed, but may cause a fatal outcome usually by a cerebrovascular attack or may cause fetal demise in pregnancy. Additionally, pathologists and urologists need to recognize that this neoplasm in most cases pursues a benign course, but aggressive forms may develop in some cases.
  • Juxtaglomerular cell tumor (JGCT) generally affects adolescents and young adults. The patients experience symptoms related to hypertension and hypokalemia due to renin-secretion by the tumor. Grossly, the tumor is well circumscribed with fibrous capsule and the cut surface shows yellow or gray-tan color with frequent hemorrhage. Histologically, the tumor is composed of monotonous polygonal cells with entrapped normal tubules. Immunohistochemically, tumor cells exhibit a positive reactivity for renin, vimentin and CD34. Ultrastructurally, neoplastic cells contain rhomboid-shaped renin protogranules. Genetically, losses of chromosomes 9 and 11 were frequently observed. Clinically, the majority of tumors showed a benign course, but rare tumors with vascular invasion or metastasis were reported. JGCT is a curable cause of hypertensive disease if it is discovered early and surgically removed, but may cause a fatal outcome usually by a cerebrovascular attack or may cause fetal demise in pregnancy. Additionally, pathologists and urologists need to recognize that this neoplasm in most cases pursues a benign course, but aggressive forms may develop in some cases. (en)
Title
  • Review of juxtaglomerular cell tumor with focus on pathobiological aspect
  • Review of juxtaglomerular cell tumor with focus on pathobiological aspect (en)
skos:prefLabel
  • Review of juxtaglomerular cell tumor with focus on pathobiological aspect
  • Review of juxtaglomerular cell tumor with focus on pathobiological aspect (en)
skos:notation
  • RIV/00669806:_____/11:10105770!RIV12-MZ0-00669806
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • V
http://linked.open...iv/cisloPeriodika
  • 1
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http://linked.open...aciTvurceVysledku
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  • 226926
http://linked.open...ai/riv/idVysledku
  • RIV/00669806:_____/11:10105770
http://linked.open...riv/jazykVysledku
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  • pathobiological aspect; juxtaglomerular cell tumor (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [0C551A939989]
http://linked.open...i/riv/nazevZdroje
  • Diagnostic Pathology
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 6
http://linked.open...iv/tvurceVysledku
  • Gatalica, Zoran
  • Hes, Ondřej
  • Kuroda, Naoto
  • Michal, Michal
  • Mikami, Shuji
  • Ohe, Chisato
  • Pan, Chin-Chen
  • Petersson, Fredrik
  • Inoue, Keiji
  • Alvarado-Cabrero, Isabel
  • Gotoda, Hiroko
  • Nagashima, Yoji
http://linked.open...ain/vavai/riv/wos
  • 000294808300001
issn
  • 1746-1596
number of pages
http://bibframe.org/vocab/doi
  • 10.1186/1746-1596-6-80
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