Myoid differentiation in dermatofibrosarcoma protuberans and its fibrosarcomatous variant: 10 years' experience in a tertiary hospital

Dermatofibrosarcoma protuberans (DFSP) is a relatively rare, locally aggressive, and dermal-based fibroblastic tumor. There are several histological variants, in which the usual emphasis is on fibrosarcomatous DFSP, as it acquires metastatic potential. Myoid differentiation in DFSP is rare, and more...

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Main Authors: Chun-hai Lo (Author), Po-man Tsang (Author), Shui-ying Cheng (Author)
Format: Book
Published: University of São Paulo, 2022-06-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Chun-hai Lo  |e author 
700 1 0 |a Po-man Tsang  |e author 
700 1 0 |a Shui-ying Cheng  |e author 
245 0 0 |a Myoid differentiation in dermatofibrosarcoma protuberans and its fibrosarcomatous variant: 10 years' experience in a tertiary hospital 
260 |b University of São Paulo,   |c 2022-06-01T00:00:00Z. 
500 |a 2236-1960 
520 |a Dermatofibrosarcoma protuberans (DFSP) is a relatively rare, locally aggressive, and dermal-based fibroblastic tumor. There are several histological variants, in which the usual emphasis is on fibrosarcomatous DFSP, as it acquires metastatic potential. Myoid differentiation in DFSP is rare, and more often found in fibrosarcomatous DFSP. Myoid differentiation is defined as tumor cells with brightly eosinophilic cytoplasm, well-defined cytoplasmic margins, and vesicular nuclei. In this study, we aim at characterizing the immunostaining pattern regarding myoid differentiation in DFSP, and discuss the potential pitfall in making the diagnosis. A total of ten cases of DFSP were found in the past ten years in our hospital. Two of them show focal myoid differentiation, including the only case of fibrosarcomatous DFSP. Around 5% of the tumor area in the traditional DFSP case shows myoid differentiation, while around 10% of the tumor area in fibrosarcomatous DFSP shows myoid differentiation. The myoid areas show positive staining, albeit patchy to focal, for smooth muscle markers, including smooth muscle actin, muscle-specific actin, caldesmon, and calponin. Staining for CD34, in those areas, is weak or negative. This may create diagnostic difficulty with smooth muscle tumors or myofibroblastic lesions, especially in a small biopsy sample. In difficult cases, the detection of COL1A1-PDGFB fusion by fluorescence in situ hybridization is helpful, as this is a characteristic chromosomal translocation found in the large majority of DFSP. 
546 |a EN 
690 |a Dermatofibrosarcoma 
690 |a Antigens 
690 |a CD34 
690 |a Muscle 
690 |a Smooth 
690 |a Medicine 
690 |a R 
690 |a Internal medicine 
690 |a RC31-1245 
655 7 |a article  |2 local 
786 0 |n Autopsy and Case Reports, Vol 12 (2022) 
787 0 |n https://www.revistas.usp.br/autopsy/article/view/199169 
787 0 |n https://doaj.org/toc/2236-1960 
856 4 1 |u https://doaj.org/article/42604b4e6a574f1fb0b0f8e1f1d6f90f  |z Connect to this object online.