By Cyril Fisher (auth.)
Soft tissue tumors are a wide and heterogeneous staff of tumors and pseudotumors with a spectrum of habit from benign to frankly malignant. This Atlas of sentimental Tissue Tumor Pathology offers an outline of reactive, pseudoneoplastic, benign and intermediate neoplasms, sarcomas and similar stipulations coming up in subcutaneous and deep smooth tissues. Emphasis is put on microscopic appearances with correlation with gross diagnostic findings the place appropriate. furthermore, the immunohistochemical and molecular genetic positive factors of the main smooth tissue tumor subtypes are provided. This compendium of sentimental tissue tumors illustrates nearly all of ailments you will definitely come across in surgical pathology.
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Extra info for Atlas of Soft Tissue Tumor Pathology
This is often a hypocellular lesion. Small multinucleated cells sometimes are seen in this variant Fig. 8 Lipofibromatosis. A component of small adipocytes sometimes termed microfat may be seen, especially at the junction of fat and cellular fibrous areas Fig. 7 Lipofibromatosis. This is a benign tumor of infancy affecting mainly the extremities, including the digits. Cellular fascicles of fibroblastic spindle cells with variable collagenization infiltrate fat. Neither component shows cytologic atypia.
Thway K, Fisher C, Sebire NJ. Pediatric fibroblastic and myofibroblastic lesions. Adv Anat Pathol. 2012;19:54–65. Yantiss RK, Nielsen GP, Lauwers GY, Rosenberg AE. Reactive nodular fibrous pseudotumor of the gastrointestinal tract and mesentery: a clinicopathologic study of five cases. Am J Surg Pathol. 2003;27:532–40. 4 Intermediate and Malignant Fibroblastic and Myoﬁbroblastic Tumors Some fibroblastic and myofibroblastic tumors are categorized as intermediate in the World Health Organization’s consensus classification of 2002.
Humphreys S, Pambakian H, McKee PH, Fletcher CD. Soft tissue chondroma–a study of 15 tumours. Histopathology. 1986;10: 147–59. Patel RM, Weiss SW, Folpe AL. Heterotopic mesenteric ossification: a distinctive pseudosarcoma commonly associated with intestinal obstruction. Am J Surg Pathol. 2006;30:119–22. Shakked RJ, Geller DS, Gorlick R, Dorfman HD. Mesenchymal chondrosarcoma: clinicopathologic study of 20 cases. Arch Pathol Lab Med. 2012;136:61–75. Wang L, Motoi T, Khanin R, Olshen A, Mertens F, Bridge J, et al.
Atlas of Soft Tissue Tumor Pathology by Cyril Fisher (auth.)