scholarly journals Exophytic gingival growth of the maxillary canine region in a young individual: Extremely rare case report of peripheral dentinogenic ghost cell tumor

2020 ◽  
Vol 16 (3) ◽  
pp. 661
Author(s):  
Monika Bansal ◽  
Rakhshinda Nahid ◽  
Kanupriya Gupta ◽  
Samidha Pandey ◽  
Preeti Tiwari ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cell Tumor ◽  
Young Individual ◽  
Ghost Cell ◽  
Maxillary Canine ◽  
Rare Case Report ◽  
Dentinogenic Ghost Cell Tumor

Dentinogenic ghost cell tumor – a rare case report

2020 ◽  
Vol 121 (2) ◽  
pp. 186-188
Author(s):  
Bonangi Ravi ◽  
G. Kamath ◽  
Srikanth Srivathsa ◽  
Medha Babshet ◽  
Usha Dayanarayana
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cell Tumor ◽  
Ghost Cell ◽  
Rare Case Report ◽  
Dentinogenic Ghost Cell Tumor

scholarly journals Dentinogenic ghost cell tumor—a rare case report with review of literature

2017 ◽  
Vol 7 (5) ◽  
pp. 598-604 ◽  
Author(s):  
Yash Agrawal ◽  
Giridhar S. Naidu ◽  
Ramanpal Singh Makkad ◽  
Ravleen Nagi ◽  
Supreet Jain ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cell Tumor ◽  
Review Of Literature ◽  
Ghost Cell ◽  
Rare Case Report ◽  
Dentinogenic Ghost Cell Tumor

PERIPHERAL DENTINOGENIC GHOST CELL TUMOR: A RARE CASE REPORT

2020 ◽  
Vol 130 (3) ◽  
pp. e183
Author(s):  
CAIO CÉSAR DA SILVA BARROS ◽  
MAURÍLIA RAQUEL DE SOUTO MEDEIROS ◽  
HÉLDER DOMICIANO DANTAS MARTINS ◽  
JOSÉ WITTOR DE MACÊDO SANTOS ◽  
JOSÉ SANDRO PEREIRA DA SILVA ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cell Tumor ◽  
Ghost Cell ◽  
Rare Case Report ◽  
Dentinogenic Ghost Cell Tumor

Glandular odontogenic cyst associated with an impacted maxillary canine: A rare case report

2016 ◽  
Vol 3 ◽  
pp. 1-4
Author(s):  
M. Vanishree ◽  
Santosh Hunasgi ◽  
Anila Koneru ◽  
Vardendra Manvikar ◽  
Surekha Ramulu
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Odontogenic Cyst ◽  
Maxillary Canine ◽  
Glandular Odontogenic Cyst ◽  
Rare Case Report

scholarly journals Urachal yolk sac tumor penetrating the bladder as a diagnostic challenge: a case report and review of the literature

2022 ◽  
Vol 17 (1) ◽  
Author(s):  
Vladimír Šámal ◽  
Tomáš Jirásek ◽  
Vít Paldus ◽  
Igor Richter ◽  
Ondřej Hes
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Yolk Sac ◽  
Cell Tumor ◽  
Yolk Sac Tumor ◽  
Review Of The Literature ◽  
Diagnostic Challenge ◽  
Macroscopic Hematuria ◽  
Rare Case Report

Abstract Background Yolk sac tumor (YST) is a germ cell tumor. It is primarily located in the gonads but can also occur extragonadally (extragonadal yolk sac tumor - EGYST), most commonly in the pelvis, retroperitoneum or mediastinum. Only a few YSTs of the urachus have been described. Case report We present a rare case report of a 37-year-old male with episodes of macroscopic hematuria. The histological specimen obtained by transurethral resection showed a solid, and in some parts papillary infiltrative, high-grade tumor with numerous areas of marked nuclear atypia and clear invasion between the detrusor bundles. Glandular pattern has been observed in only minority of the tumor. Immunohistochemistry showed significant positivity for GPC3, SALL4 and cytokeratins AE1/AE3, while KRT7 and GATA3 were negative. We concluded that the biopsy findings were consistent with urothelial carcinoma with infrequent YST differentiation. In definitive surgical specimens we found a malignant epithelial, glandular and cystically arranged tumor of germinal appearance arising from urachus. The surrounding urothelium was free of invasive or in situ tumor changes. We reclassified the tumor as a urachal YST. Conclusion EGYST was suspected because glandular and hepatoid structures were found, but the presence of these structures should be verified by immunohistochemistry.

scholarly journals Testicular Adult Type Granulosa Cell Tumor: A Very Rare Case Report and Review of Literature

2017 ◽  
Vol 1 (1) ◽  
pp. 12-14 ◽  
Author(s):  
Wei-Chieh Chen ◽  
◽  
Yun-Ho Lin ◽  
Shauh-Der Yeh ◽  
Chien-Chih Wu ◽  
...  
Keyword(s):  
Case Report ◽  
Granulosa Cell ◽  
Rare Case ◽  
Granulosa Cell Tumor ◽  
Cell Tumor ◽  
Review Of Literature ◽  
Adult Type ◽  
Rare Case Report
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