Villoglandular papillary adenocarcinoma of the uterine cervix: A diagnostic challenge

2009 ◽  
Vol 88 (3) ◽  
pp. 355-358 ◽  
Author(s):  
Jacob Korach ◽  
Ronit Machtinger ◽  
Tamar Perri ◽  
Daniel Vicus ◽  
Jacob Segal ◽  
...  
2016 ◽  
Vol 2016 ◽  
pp. 1-3
Author(s):  
Shomaila Aamir M. Akbar ◽  
Mutahir A. Tunio ◽  
Sadeq Al-Dandan ◽  
Kareema Mohammed Y. Salamah ◽  
Mushabbab AlAsiri

Introduction. Papillary squamotransitional cell carcinoma (PSTCC) is an uncommon histopathological variant of squamous cell carcinoma (SCC) of the uterine cervix, which occurs in postmenopausal women.Presentation of Case. Herein, we describe a case of a 63-year-old woman who presented with 4-month history of postmenopausal vaginal bleeding. Vaginal examination revealed a fragile lesion of size1×1 cm invading left posterior vaginal fornice and parametrium. Biopsy showed the presence of papillae containing fibrovascular cores lined by multilayered atypical epithelial cells resembling squamous and transitional cell epithelium, confirming the diagnosis of PSTCC of the uterine cervix. After staging work-up she was staged according to the International Federation of Gynecology and Obstetrics (FIGO) staging system 2009 as FIGO IIB, and she was started on extended field concurrent chemoradiation.Discussion. PSTCC of the uterine cervix is an extremely rare and aggressive entity. PSTCC is often characterized by the presence of papillary structures with prominent fibrovascular cores. PSTCC of the uterine cervix should be differentiated from transitional cell carcinoma, squamous papilloma, papillary adenocarcinoma, and cervical intraepithelial neoplasia with papillary features.Conclusion. PSTCC of the uterine cervix is a diagnostic challenge; further studies regarding the mechanism underlying the development of PSCC are warranted.


2003 ◽  
Vol 127 (1) ◽  
pp. e28-e31
Author(s):  
Edgar G. Fischer ◽  
Thèrése J. Bocklage ◽  
Ian Rabinowitz ◽  
Harriet O. Smith ◽  
David S. Viswanatha

Abstract Primary plasmacytomas of the female genital tract are extremely rare and present a substantial diagnostic challenge. Five cases morphologically representing plasmacytomas and localized to the uterine cervix have been reported previously; however, only 1 was shown to be monotypic for immunoglobulin light-chain expression. We report the case of a 37-year-old woman who had highly atypical plasma cells on her Papanicolaou test. A clinically detected endocervical polyp was removed and revealed a plasmacytoma, the diagnosis of which was substantiated by demonstrating monotypic λ-light-chain restriction and a clonal immunoglobulin heavy-chain gene rearrangement. The cytologic and histopathologic findings of plasmacytomas of the uterine cervix are discussed, including the utility of immunophenotypic and molecular techniques to confirm the neoplastic diagnosis.


2015 ◽  
Vol 11 (1) ◽  
pp. 837-841 ◽  
Author(s):  
QIANG-YONG ZHOU ◽  
HAI-YAN CHEN ◽  
SI-MENG YANG ◽  
YUE-HUA LI ◽  
XUE-QING WU

2004 ◽  
Vol 202 (4) ◽  
pp. 305-310 ◽  
Author(s):  
Murat Dede ◽  
Güzin Deveci ◽  
M. Salih Deveci ◽  
Mufit Cemal Yenen ◽  
Umit Goktolga ◽  
...  

2002 ◽  
Vol 41 (6) ◽  
pp. 448-452
Author(s):  
Masato NISHIMURA ◽  
Makoto HIROI ◽  
Mikio MIYAUCHI ◽  
Hiromi IOKI ◽  
Natsu SAKIMOTO ◽  
...  

2012 ◽  
Vol 48 (6) ◽  
pp. 216-217 ◽  
Author(s):  
Alberto Caballero Vázquez ◽  
Cintia María Merinas López ◽  
Ana Dolores Romero Ortiz

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