New or unusual dermatopathology tumors: a review

被引:15
作者
Lewin, Marc Roy [1 ,2 ]
Montgomery, Elizabeth A. [3 ]
Barrett, Terry L. [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Propath Dermatopathol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Sch, Dallas, TX USA
[3] Johns Hopkins Hosp Pathol, Baltimore, MD 21287 USA
关键词
myxoinflammatory fibroblastic sarcoma; pleomorphic hyalinizing angiectatic tumor; primitive non-neural granular cell tumor; soft tissue tumor; superficial acral fibromyxoma; HYALINIZING ANGIECTATIC TUMOR; SUPERFICIAL ACRAL FIBROMYXOMA; MYXOINFLAMMATORY FIBROBLASTIC SARCOMA; FIBROHISTIOCYTIC LIPOMATOUS LESION; CELLULAR DIGITAL FIBROMAS; SOFT PARTS; CUTANEOUS MYOEPITHELIOMA; DERMATOFIBROSARCOMA PROTUBERANS; IMMUNOHISTOCHEMICAL ANALYSIS; CLINICOPATHOLOGICAL ANALYSIS;
D O I
10.1111/j.1600-0560.2011.01767.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
As experience is acquired, there is a constant evolution in both terminology and understanding of various relatively newly described tumors in the realm of dermatopathology. Several mesenchymal tumors of the lower extremity have undergone various changes in nomenclature, molecular discoveries, and histologic grading. Examples include hemosiderotic fibrohistiocytic lipomatous lesion/pleomorphic hyalinizing angiectatic tumor; superficial acral fibromyxoma; and myxoinflammatory fibroblastic sarcoma. Primary cutaneous myoepithelioma is also a relatively newly described entity for which grading and classification continue to evolve. Finally, even our understanding of the classic granular cell tumor has expanded to include a non-neural variant. This article reviews the current nomenclature, emerging concepts, and differential diagnosis of these evolving entities.
引用
收藏
页码:689 / 696
页数:8
相关论文
共 55 条
[1]   Primitive nonneural granular cell tumor (so-called atypical polypoid granular cell tumor). Report of 2 cases with immunohistochemical and ultrastructural correlation [J].
Al Habeeb, Ayman ;
Salama, Samih .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2008, 30 (02) :156-159
[2]   Superficial acral fibromyxoma: a clinicopathological analysis of 32 tumors including 4 in the heel [J].
Al-Daraji, Wael I. ;
Miettinen, Markku .
JOURNAL OF CUTANEOUS PATHOLOGY, 2008, 35 (11) :1020-1026
[3]   Consistent t(1;10) with Rearrangements of TGFBR3 and MGEA5 in Both Myxoinflammatory Fibroblastic Sarcoma and Hemosiderotic Fibrolipomatous Tumor [J].
Antonescu, Cristina R. ;
Zhang, Lei ;
Nielsen, G. Petur ;
Rosenberg, Andrew E. ;
Dal Cin, Paola ;
Fletcher, Christopher D. M. .
GENES CHROMOSOMES & CANCER, 2011, 50 (10) :757-764
[4]   Polypoid S-100-negative granular cell tumor of the oral cavity: A case report and review of literature [J].
Basile, JR ;
Woo, SB .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 2003, 96 (01) :70-76
[5]   Myxoinflammatory fibroblastic sarcoma:: investigations by comparative genomic hybridization of two cases and review of the literature [J].
Baumhoer, Daniel ;
Glatz, Kathrin ;
Schulten, Hans-Juergen ;
Fuezesi, Laszlo ;
Fricker, Renato ;
Kettelhack, Christoph ;
Hasenboehler, Paula ;
Oberholzer, Martin ;
Jundt, Gernot .
VIRCHOWS ARCHIV, 2007, 451 (05) :923-928
[6]   Myoepithelioma with melanocytic colonization (melanocytic myoepithelioma): a case report [J].
Bernaba, Bob N. ;
Binder, Scott W. ;
Cassarino, David S. .
JOURNAL OF CUTANEOUS PATHOLOGY, 2009, 36 (06) :697-701
[7]  
Betlach J, 2006, Cesk Patol, V42, P191
[8]   Haemosiderotic fibrolipomatous tumour (so-called haemosiderotic fibrohistiocytic lipomatous tumour): analysis of 13 new cases in support of a distinct entity [J].
Browne, TJ ;
Fletcher, CDM .
HISTOPATHOLOGY, 2006, 48 (04) :453-461
[9]   Pleomorphic hyalinizing angiectatic tumor of soft parts:: Ultrastructural analysis of a case with original features [J].
Capovilla, Mathieu ;
Birembaut, Philippe ;
Cucherousset, Joël ;
Ploton, Dominique ;
de Saint-Maur, Paul P. ;
Fléjou, Jean-François ;
Lesec, Guy .
ULTRASTRUCTURAL PATHOLOGY, 2006, 30 (1-2) :59-64
[10]   Dermal non-neural granular cell tumour (so-called primitive polypoid granular cell tumour): a distinctive entity further delineated in a clinicopathological study of 11 cases [J].
Chaudhry, IH ;
Calonje, E .
HISTOPATHOLOGY, 2005, 47 (02) :179-185