Reconsidering the Diagnostic and Prognostic Utility of LN-2 for Undifferentiated Pleomorphic Sarcoma and Atypical Fibroxanthoma

被引:12
作者
Hollmig, S. Tyler [1 ]
Rieger, Kerri E. [1 ,2 ]
Henderson, Michael T. [1 ]
West, Robert B. [2 ]
Sundram, Uma N. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Dermatol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
关键词
undifferentiated pleomorphic sarcoma; malignant fibrous histiocytoma; pleomorphic dermal sarcoma; atypical fibroxanthoma; LN-2; CD74; immunohistochemistry; MALIGNANT FIBROUS HISTIOCYTOMA; TISSUE MICROARRAYS; SURGERY; TUMORS;
D O I
10.1097/DAD.0b013e318265fb9e
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The topic of distinguishing atypical fibroxanthoma (AFX) from undifferentiated pleomorphic sarcoma (UPS), formerly malignant fibrous histiocytoma, is highly controversial. Although their clinical behavior is disparate, AFX and UPS commonly appear nearly identical on routine histopathologic examination. Although conceptually useful, subcategorization of UPS into superficial (confined to the dermis and subcutaneous tissue) and deep (involvement of fascia and deeper structures) types has not improved our ability to differentiate UPS from AFX. Numerous authors have purported LN-2 (CD74) immunopositivity as able to distinguish UPS from AFX and to predict those rare AFX likely to behave aggressively, although only a single prior study has been dedicated to evaluating this marker. We performed LN-2 staining of 14 AFX, 8 superficial UPS, and 65 deep UPS specimens using an identical protocol as described by prior authors. Of the 73 total UPS specimens, only 1 (1.4%) stained strongly with LN-2, as compared with 3 of 14 (21%) AFX (P = 0.012). One of 2 (50%) clinically aggressive AFX tumors that later exhibited both local recurrence and metastasis stained strongly for LN-2, whereas 2 of 12 (17%) of the more indolent tumors stained strongly with this marker (P = 0.40). Our data do not replicate prior reports of LN-2 as a sensitive and specific marker for UPS, or as indicative of prognosis for AFX, and therefore does not support the use of LN-2 as either a diagnostic or prognostic marker.
引用
收藏
页码:176 / 179
页数:4
相关论文
共 26 条
[1]   TREATMENT OF MALIGNANT FIBROUS HISTIOCYTOMA AND ATYPICAL FIBROUS XANTHOMAS WITH MICROGRAPHIC SURGERY [J].
BROWN, MD ;
SWANSON, NA .
JOURNAL OF DERMATOLOGIC SURGERY AND ONCOLOGY, 1989, 15 (12) :1287-1292
[2]   Metastasizing atypical fibroxanthoma (cutaneous malignant histiocytoma): Report of five cases [J].
Cooper, JZ ;
Newman, SR ;
Scott, GA ;
Brown, MD .
DERMATOLOGIC SURGERY, 2005, 31 (02) :221-225
[3]   MOHS SURGERY REPORT - SPINDLE CELL FIBROHISTIOCYTIC TUMORS - CLASSIFICATION AND PATHO-PHYSIOLOGY [J].
DZUBOW, LM .
JOURNAL OF DERMATOLOGIC SURGERY AND ONCOLOGY, 1988, 14 (05) :490-495
[4]  
ENZINGER FM, 1988, SOFT TISSUE TUMORS, P269
[5]   Tissue microarrays are an effective quality assurance tool for diagnostic immunohistochemistry [J].
Hsu, FD ;
Nielsen, TO ;
Alkushi, A ;
Dupuis, B ;
Huntsman, D ;
Liu, CL ;
van de Rijn, M ;
Gilks, CB .
MODERN PATHOLOGY, 2002, 15 (12) :1374-1380
[6]   Mohs micrographic surgery for the treatment of spindle cell tumors of the skin [J].
Huether, MJ ;
Zitelli, JA ;
Brodland, DG .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2001, 44 (04) :656-659
[7]   Atypical Fibroxanthoma: A Review of the Literature [J].
Iorizzo, Luciano J., III ;
Brown, Marc D. .
DERMATOLOGIC SURGERY, 2011, 37 (02) :146-157
[8]   Multiple recurrent atypical fibroxanthomas/superficial malignant fibrous histiocytomas of the forehead excised with Mohs micrographic surgery [J].
Jensen, KJ ;
Peterson, SR .
DERMATOLOGIC SURGERY, 2006, 32 (04) :588-591
[9]  
Kahn H. J., 1996, Journal of Cutaneous Pathology, V23, P79
[10]  
KEARNEY MM, 1980, CANCER-AM CANCER SOC, V45, P167, DOI 10.1002/1097-0142(19800101)45:1<167::AID-CNCR2820450127>3.0.CO