By Cyril Fisher MD, Elizabeth Montgomery MD, Khin Thway BSc MBBS FRCPath
Biopsy Interpretation of soppy Tissue Tumors is a pragmatic consultant and bench reference for surgical pathologists for the translation of soppy tissue biopsies, together with open and percutaneous center needle biopsies. every one bankruptcy courses readers in a logical manner, with the most important differential diagnostic beneficial properties of particular tumors distinct inside of each one classification, utilizing morphologic, immunohistochemical, ultrastructural, and genetic facts. This parallels and enhances the conventional diagnostic strategy. as well as colour photomicrographs the ebook comprises a variety of tables for differential prognosis of particular morphologic gains and use of immunohistochemical panels. appropriate scientific and administration issues impacted through the pathologic analysis are integrated.
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Additional info for Biopsy Interpretation of Soft Tissue Tumors
Peripheral collagen bundles, rare foamy, and giant cells. Central necrosis in some. Atypical variant has scattered enlarged hyperchromatic nuclei or multinucleation in background of typical cells Infiltrative tumor with variable mixture of (1) cellular fibrous bands containing small stellate or ovoid cells, (2) neurofibroma-like spindle cell component, (3) mature fat. 1. Nodular Fasciitis. This early stage lesion shows fascicles and files of myofibroblasts in myxoid stroma. There are lymphocytes and red blood cells in the stroma.
The stroma is at first myxoid (Fig. 1, e-Fig. 1). Later, there is increased cellularity with a vague storiform pattern (e-Fig. 2). 2. Nodular Fasciitis. Cellular phase displays sheets of bland cells with ill-defined storiform pattern. The cells have ovoid nuclei and small nucleoli, with scattered mitoses. Note the focal stromal microcysts. there remain small microcysts containing a few extravasated red blood cells and lymphocytes, around which the spindle cells are curved (crescent sign) (e-Figs.
37) and should not be mistaken for rhabdomyoblasts or other malignant cells. Low-grade fibromyxoid sarcoma (see Chapters 10 and 21) can resemble fibromatosis but lacks myofibroblastic nuclear features and has whorled fibromyxoid areas and cellular myxoid foci. In addition, it has diagnostic genetic abnormalities. 10 Fibromatosis. Nuclear immunoreactivity for beta catenin. The staining is finely granular. Careful observation is required as some cells have similar paranuclear positivity. Ancillary Investigations The lesional cells express SMA and occasionally (and very focally) desmin but lack h-caldesmon, CD34, and (usually) S100 protein.