scholarly journals Extrarenal Rhabdoid Tumor of the Prostate

2020 ◽  
Author(s):  
Keyword(s):  
Rhabdoid Tumor ◽  
Extrarenal Rhabdoid Tumor

Intradural lumbosacral malignant extrarenal rhabdoid tumor: a case report

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

Malignant extrarenal rhabdoid tumor of parapharyngeal space: A rare presentation

2019 ◽  
Vol 2 (1) ◽  
pp. 15
Author(s):  
S Pasricha ◽  
N Patnaik ◽  
Meenakshi Kamboj ◽  
Gurudutt Gupta ◽  
Anurag Mehta
Keyword(s):  
Parapharyngeal Space ◽  
Rhabdoid Tumor ◽  
Rare Presentation ◽  
Extrarenal Rhabdoid Tumor

scholarly journals Cutaneous extrarenal rhabdoid tumor in a dog: a case report

2016 ◽  
Vol 60 (No. 2) ◽  
pp. 115-119
Author(s):  
HJ Kim ◽  
EJ Choi ◽  
HR Lee ◽  
BT Kwon ◽  
SH Do
Keyword(s):  
Case Report ◽  
Rhabdoid Tumor ◽  
Extrarenal Rhabdoid Tumor

Isochromosome (12p) and Peritriploidy in a Highly Malignant Extrarenal Rhabdoid Tumor

1999 ◽  
Vol 109 (2) ◽  
pp. 175-177 ◽  
Author(s):  
P.P.F.Grandjean Perrenod Comtesse ◽  
A Simons ◽  
A Siepman ◽  
F Stellink ◽  
R.F Suijkerbuijk ◽  
...  
Keyword(s):  
Rhabdoid Tumor ◽  
Isochromosome 12P ◽  
Extrarenal Rhabdoid Tumor

Malignant Extrarenal Rhabdoid Tumor in a 5-Month-Old Male With Mediastinal and Heart/Great Vessel Involvement

2020 ◽  
Vol 154 (Supplement_1) ◽  
pp. S53-S54
Author(s):  
H Khokhar ◽  
R Craver ◽  
M Stark
Keyword(s):  
Electron Microscopy ◽  
Rhabdoid Tumor ◽  
High Power Field ◽  
Pediatric Malignancy ◽  
Multiple Modalities ◽  
Rhabdoid Cells ◽  
S 100 ◽  
Great Vessels ◽  
Clear Cytoplasm ◽  
Extrarenal Rhabdoid Tumor

Abstract Introduction/Objective Extrarenal rhabdoid tumor is a high-grade soft-tissue predominately pediatric malignancy with a frequency of 0.15 per million children less than 15 years. It is associated with del(22) (q11.2) with SMARCB1 loss, recognized by loss of INI-1 staining. It has distinct perinuclear hyaline inclusions; however, this feature can be present in other tumors. We describe a malignant extrarenal rhabdoid tumor involving the heart and great vessels to highlight the multiple modalities required for the diagnosis of this tumor in this unusual location. Methods We utilized routine histology, immunohistochemistry, and electron microscopy. Results This 5 -month -old male presented with respiratory distress due to a mass that invaded the heart, surrounding the great vessels. The tumor was composed of sheets of polygonal large cells with light pink to clear cytoplasm, eccentric nuclei with mild anisonucleosis, peripherally marginating chromatin, prominent nucleoli, with 2 mitoses per 10 high power field. Hyaline perinuclear inclusions were inapparent. There were frequent clusters of lymphocytes and eosinophils, with 10 percent necrosis and moderately increased vascularity. The tumor was positive for vimentin, SMA, EMA, MSA, S-100, keratin, and WT1, and negative for INI-1, CD34, ALK, AFP, PLAP, CD30, myogenin, NeuN1, synaptophysin, chromogranin, and NSE. Electron microscopy demonstrated occasional cells with perinuclear collections of intermediate filaments, some with whorls. The strong positivity for vimentin, keratin, SMA, MSA, S-100, negative staining for INA-1 and CD34, and visualization of perinuclear intermediate filament whorls by electron microscopy helped make the diagnosis of extrarenal rhabdoid tumor. Conclusion Malignant extrarenal rhabdomyosarcomas may occur in the middle mediastinum, invade the heart, occur in the first 6 months of life, and not have the typical rhabdoid cells. Diagnoses depend on multiple modalities

Malignant extrarenal rhabdoid tumor: a case report

2015 ◽  
Vol 4 (1) ◽  
Author(s):  
Tanja Stüber ◽  
Eric Frieauff ◽  
Joachim Diessner ◽  
Arnd Hönig ◽  
Monika Rehn
Keyword(s):  
Fetal Distress ◽  
Rhabdoid Tumor ◽  
First Year ◽  
Therapeutic Trial ◽  
Male Fetus ◽  
Preterm Baby ◽  
Histopathologic Analysis ◽  
The Right ◽  
First Year Of Life ◽  
Extrarenal Rhabdoid Tumor

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.

Adult Extrarenal Rhabdoid Tumor of the Lacrimal Gland

Ophthalmology ◽  
1992 ◽  
Vol 99 (4) ◽  
pp. 567-574 ◽  
Author(s):  
John H. Niffenegger ◽  
Frederick A. Jakobiec ◽  
John W. Shore ◽  
Daniel M. Albert
Keyword(s):  
Lacrimal Gland ◽  
Rhabdoid Tumor ◽  
Extrarenal Rhabdoid Tumor

scholarly journals Inv(11)(p13p15) and Myf-3(MyoD1) in a Malignant Extrarenal Rhabdoid Tumor of a Premature Newborn

2000 ◽  
Vol 48 (4) ◽  
pp. 463-467 ◽  
Author(s):  
Franziska Staehelin ◽  
Heidi Bissig ◽  
Irene Hösli ◽  
David R Betts ◽  
Beat W Schäfer ◽  
...  
Keyword(s):  
Rhabdoid Tumor ◽  
Premature Newborn ◽  
Extrarenal Rhabdoid Tumor
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