Atypical fibroxanthoma relapse as pleomorphic dermal sarcoma after slow Mohs micrographic surgery

Author(s):  
Cristina López‐Llunell ◽  
Mireia Yébenes ◽  
Patricia Garbayo‐Salmons ◽  
Lorena Leal ◽  
Alfonso Mogedas‐Vergara
1997 ◽  
Vol 23 (2) ◽  
pp. 105-110 ◽  
Author(s):  
JAIME L. DAVIS ◽  
HENRY W. RANDLE ◽  
MARK J. ZALLA ◽  
RANDALL K. ROENIGK ◽  
DAVID G. BRODLAND

2014 ◽  
Vol 71 (4) ◽  
pp. 842-845
Author(s):  
Carolin Zschoche ◽  
Corinna Hamsch ◽  
Heinz Kutzner ◽  
Thomas Mentzel ◽  
Siegfried Werchau ◽  
...  

Oncotarget ◽  
2018 ◽  
Vol 9 (30) ◽  
pp. 21182-21189 ◽  
Author(s):  
Timo Gaiser ◽  
Daniela Hirsch ◽  
Azadeh Orouji ◽  
Marisa Bach ◽  
Peter Kind ◽  
...  

2019 ◽  
Vol 37 (3) ◽  
pp. 253-259 ◽  
Author(s):  
Teo Soleymani ◽  
Sumaira Z. Aasi ◽  
Roberto Novoa ◽  
S. Tyler Hollmig

2017 ◽  
Vol 1 (3) ◽  
pp. 169-172
Author(s):  
Timothy Nyckowski ◽  
Roger Ceilley ◽  
Andrew Bean

Atypical fibroxanthoma (AFX) is a rare, dermal- based mesenchymal neoplasm. Clinically, these tumors are characterized by rapid, exophytic growth and epidermal ulceration.1 Despite striking clinical features and growth pattern, it is considered to be a tumor of low- to intermediate- malignant potential.1-3. We report a case of an 89 year old Caucasian male that had a 1 month history of a rapidly enlarging, pedunculated neoplasm on the scapha of his right ear. Histologic and immunohistochemical analysis of the lesion were consistent with atypical fibroxanthoma. After a biopsy, the patient underwent a complete resection with Mohs micrographic surgery and remains asymptomatic 6 months later. This 3.0 x 2.0 cm lesion emerged over a 4-5 week period, representing the most rapid growing AFX of the external ear reported in the literature.


2018 ◽  
Vol 79 (5) ◽  
pp. 929-934.e6 ◽  
Author(s):  
Stanislav N. Tolkachjov ◽  
Benjamin F. Kelley ◽  
Fares Alahdab ◽  
Patricia J. Erwin ◽  
Jerry D. Brewer

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