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Table 5 Differential diagnoses of SFT (in accordance with Fletcher et al. and Doyle et al.[1],[11])

From: Solitary fibrous tumor – clinicopathologic, immunohistochemical and molecular analysis of 28 cases

 

Histopathological characteristics

IHC

Genetic alterations

Dedifferentiated liposarcoma

lipogenic component with atypia

MDM2 +, CDK4 +

amplification MDM2

 

atypia in dediff. component can be mild

STAT6 −/+

 

Deep benign fibrous histiocytoma

storiform or short fascicles, branching vasculature

CD34 +/−, SMA f+/−, STAT6 −/+

 

Spindle cell lipoma

short stubby nuclei, ropey collagen

CD34+

RB1 deletion

 

variable proportions of fat

  

Cellular angiofibroma

short stubby nuclei, wispy collagen

CD34 +/−, desmin −/+

RB1 deletion

 

numerous (hyalinized) vessels

SMA −/+,

 

Mammary type myofibroblastoma

(long) fascicles, short stubby nuclei

CD34 +, desmin +

RB1 deletion

 

broad bands collagen

SMA −/+,

 

Myofibroma

biphasic, immature spindle cells and mature myoid cells, bluish matrix, branching vessels

SMA +/−, desmin −/+, CD34 −/+

 

Dermatofibrosarcoma protuberans

storiform, short fascicles, uniform spindle cells, “honeycomb” appearance of fat

CD34 +

COL1A1-PDGFB

Monophasic synovial sarcoma

cellular fascicles, uniform spindle cells

TLE1 +, EMA +, CK +

SYT-SSX1/2

Cellular schwannoma

short bundles, interlacing fascicles

S100 +

NF2 mutations

 

tapered nuclei, hyalinized (ectatic) vessels

  

Perineurioma

storiform, whorled growth, bipolar cells, uniform oval or tapering nuclei

CD34 +/−, EMA +, Claudin-1−/+, GLUT1 −/+

 

Low-grade fibromyxoid sarcoma

alternating hypo- and more cellular fascicles and whorls, fibrous and myxoid background, bland spindle cells

MUC4 +, EMA +

FUS-CREB3L1/2

Inflammatory myofibroblastic tumor

fascicles of myofibroblasts, myxoid or

SMA +/−, desmin +/−

ALK rearrangement +/−

 

collagenous background, inflammation

ALK +/−

 

Sarcomatoid mesothelioma

fascicles or haphazard distribution, atypical spindle cells

CK, EMA, D2-40, caretinin, WT1

BAP1 mutation [23]

Inflammatory fibroid polyp

onion-skin pattern, short fascicles

CD34 +/−

PDGFRA mutation

of the GI tract [24] cells,

prominent vasculature, inflammatory especially eosinophils

  

Soft tissue angiofibroma [25]

variably collagenous and myxoid areas

EMA +/−, CD34 −/+

GTF2I-NCOA2[26]

 

numerous small branching capillaries

 

AHRR-NCOA2[27]