Mesenchymal chondrosarcoma of the foot, an unusual location: Case report and review of the literature

Author(s):  
Miquel Sans ◽  
Dolors Nubiola ◽  
Maria Alejo ◽  
Francesc Diaz ◽  
Antoni Anglada ◽  
...  
2019 ◽  
Vol 52 (4) ◽  
pp. 260-264
Author(s):  
David A. Suarez-Zamora ◽  
Paula A. Rodriguez-Urrego ◽  
Jose A. Hakim-Tawil ◽  
Mauricio A. Palau-Lazaro

2004 ◽  
Vol 7 (6) ◽  
pp. 653-660 ◽  
Author(s):  
Dinesh Rakheja ◽  
Kathleen S. Wilson ◽  
John J. Meehan ◽  
Roger A. Schultz ◽  
Gerhard E. Maale ◽  
...  

We report a case of a benign solitary fibrous tumor that occurred in the right shoulder of a 9-year-old girl. This case is remarkable due to the unusual location of its occurrence and the young age of the patient. In addition, cytogenetic analysis revealed a karyotype unreported in this neoplasm: 46,XX,der(4)t(4;9)(q31.1;q34), del(9)(p22p24),der(9)t(4;9)(q31.1;q34)ins(9;?)(q34;?) (17 cells)/46,XX (3 cells).


2015 ◽  
Vol 10 (2) ◽  
pp. 1075-1078 ◽  
Author(s):  
DUQUN CHEN ◽  
ZI YE ◽  
XIONGHUI WU ◽  
BENTAO SHI ◽  
LIJUN ZHOU ◽  
...  

Cases Journal ◽  
2009 ◽  
Vol 2 (1) ◽  
Author(s):  
Nexhmi Sh Hyseni ◽  
Sadik S Llullaku ◽  
Defrim H Koçinaj ◽  
Hysni J Jashari ◽  
Baton Z Kelmendi

2016 ◽  
Vol 2016 ◽  
pp. 1-3
Author(s):  
A. Coutellier ◽  
I. Théate ◽  
O. Vanhooteghem

Onychomatricoma is a rare and benign tumour of the nail matrix but originates rarely from the ventral portion of the proximal nail fold. This tumour is characterised by fingerlike projections that invade the nail plate. This lesion, of unknown aetiology, is typically asymptomatic with slow progression. Localisation on the finger is the most frequently described. We report the case of a 68-year-old woman who has an onychomatricoma in an unusual location, the fifth toe of the left foot. Due to its clinical appearance, the tumour can be confused with and treated as onychomycosis. However, if it is resistant to an oral antifungal well behaved treatment, one must consider onychomatricoma diagnosis.


2000 ◽  
Vol 86 (1) ◽  
pp. 75-78 ◽  
Author(s):  
Roberto Biagini ◽  
Umberto Orsini ◽  
Silvio Demitri ◽  
Pietro Ruggieri ◽  
Stefano Ferrari ◽  
...  

2019 ◽  
Vol 129 ◽  
pp. 302-310 ◽  
Author(s):  
Saman Shabani ◽  
Mayank Kaushal ◽  
Bruce Kaufman ◽  
Jeffrey Knipstein ◽  
Michael W. Lawlor ◽  
...  

2008 ◽  
Vol 11 (4) ◽  
pp. 309-313 ◽  
Author(s):  
Rossella De Cecio ◽  
Ilenia Migliaccio ◽  
Jessica Falleti ◽  
Marialaura Basso Del De Caro ◽  
Guido Pettinato

2017 ◽  
Vol 2017 ◽  
pp. 1-3 ◽  
Author(s):  
Elena Vargas-Laguna ◽  
Adrián Imbernón-Moya ◽  
Antonio Aguilar-Martínez ◽  
Fernando Burgos

Warty dyskeratoma is an uncommon entity characterized by a solitary keratotic papule or nodule usually located in the head and neck of young adults. The histopathology shows a pattern of acantholytic dyskeratosis. We report a 32-year-old man who presented pain, serous exudation, a distal onycholysis with subungual hyperkeratosis, and roundish erythronychia in the nail plate of his left first toe 2 years ago. A histopathologic diagnosis of subungual warty dyskeratoma was made. When dealing with focal acantholytic dyskeratosis several differential diagnoses should be considered including Darier’s disease, transient focal acantholytic dyskeratosis or Grover disease, and Hailey-Hailey disease. We present an unusual location of warty dyskeratoma in the nail bed using a clinicohistopathological correlation for the diagnosis.


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