Prenatal detection of congenital malignant extrarenal rhabdoid tumor primarily involving the right upper extremity that ruptured in utero

2009 ◽  
Vol 29 (8) ◽  
pp. 819-821 ◽  
Author(s):  
Ja-Young Kwon ◽  
Kook In Park ◽  
Ki Seok Lee ◽  
Woo Ick Yang ◽  
Young-Han Kim
2015 ◽  
Vol 4 (1) ◽  
Author(s):  
Tanja Stüber ◽  
Eric Frieauff ◽  
Joachim Diessner ◽  
Arnd Hönig ◽  
Monika Rehn

AbstractThe fetal extrarenal rhabdoid tumor is a highly aggressive and rare neoplasm that mostly occurs in the first year of life. In this case, a remarkably enlarged right upper arm was diagnosed in a male fetus at 31+2 weeks of gestation. Because of a fast progressive tumor volume and signs of fetal distress, a cesarean section was performed at 34 weeks of gestation. The preterm baby showed a blue livid tumor reaching from the right elbow up to the shoulder that resulted in an extrarenal rhabdoid tumor on histopathologic analysis. A therapeutic trial with cyclophosphamide was not effective and the child died at the age of 26 days because of multi-organ failure.


2015 ◽  
Vol 15 (1) ◽  
pp. 123-126 ◽  
Author(s):  
Laura Gigante ◽  
Irene Paganini ◽  
Marina Frontali ◽  
Serena Ciabattoni ◽  
Federica Carla Sangiuolo ◽  
...  

2017 ◽  
Vol 34 (1) ◽  
pp. 165-167 ◽  
Author(s):  
Richard Justin Garling ◽  
Rasanjeet Singh ◽  
Carolyn Harris ◽  
Abilash Haridas

2013 ◽  
Vol 3 (4) ◽  
pp. e124
Author(s):  
Jonathan M. Frank ◽  
Jeffrey J. Eckardt ◽  
Scott D. Nelson ◽  
Leanne Seeger ◽  
Noah Federman

Author(s):  
C. V. Schenone ◽  
A. King ◽  
E. Castro ◽  
P. Ketwaroo ◽  
R. Donepudi ◽  
...  

2020 ◽  
Vol 12 (4) ◽  
pp. 337-340
Author(s):  
Niki Tadayon ◽  
Sina Zarrintan ◽  
Seyed Mohammad Reza Kalantar-Motamedi

We report a case of 66-year-old woman with true aneurysm of the right brachial artery. She presented with acute upper extremity ischemia. The hand was cold and parenthesized and distal pulses were absent. CT angiography (CTA) revealed a 20*25 mm true brachial artery aneurysm. The aneurysm was thrombosed without distal run-off. We excised the aneurysm and reestablished the arterial flow by a reverse saphenous interposition graft. The postoperative course was uneventful.


1995 ◽  
Vol 20 (3) ◽  
pp. 319-326 ◽  
Author(s):  
J. ROBINSON ◽  
K. C. OBERG ◽  
W. M. KIRSCH ◽  
V. E. WOOD

39 foetal mice with genetic syndactyly were identified in utero at 17 days of gestation, and the right hindfoot extruded through the uterus. The syndactylous digits were separated by simple incisions. In one group (n = 25) digit separation was maintained during wound healing by the interdigital application of a silver microclip. Digit separation was also assessed in a second group of newborn mice less than 24 hours old (juxtanatal population, n = 24). Two foetuses (5%) and six newborns (25%) developed digital necrosis following microclip application. In the remaining microchlipped animals (23 intrauterine and 10 juxtanatal), microclip application maintained digit separation, allowing wound healing to occur with epithelialization of the separated digits. No inflammation or scar formation occurred. In the third group (n = 22) without microclip application, the digital skin reapproximated and webbing recurred during wound healing. These studies demonstrate the need to maintain digit separation during wound healing following intra-uterine or juxtanatal syndactyly repair.


2019 ◽  
Vol 2 (1) ◽  
pp. 15
Author(s):  
S Pasricha ◽  
N Patnaik ◽  
Meenakshi Kamboj ◽  
Gurudutt Gupta ◽  
Anurag Mehta

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