International Journal of Surgical Pathology · 2004 · 31 citations · 34 references
MedicineOncologyPathologyAnatomic PathologyGastrointestinal OncologyTumor PathologyBenign NeoplasmsBenign TumorsGastrointestinal NeoplasmsGastrointestinal PathologyGastrointestinal Stromal TumorsNeoplastic PathologyGastrointestinal MalignancySmall Bowel Gastrointestinal Stromal TumorsSmall Intestinal Gastrointestinal Stromal TumorsSmall Intestinal NeoplasmsSmooth Muscle HistologyUltrastructural Pathology
Eight cases of reactive nodular fibrous pseudotumor of the gastrointestinal tract are presented. The patients included 6 males and 2 females between the ages of 1 and 68 years (mean age 41.5 years). Three tumors involved the small intestine, and 5 of the investigated lesions were located in the large bowel. Of these, 2 originated in the sigmoid colon, 1 in the cecum, 1 in the appendix, and 1 in the large bowel not otherwise specified. The tumors' size varied from 3 to 10 cm in the greatest diameter (mean 6.2 cm). Histologically they were composed of stellate or spindle shaped cells resembling fibroblasts arranged haphazardly or in intersecting fascicles, embedded in a collagen-rich stroma, with sparse intralesional mononuclear cells frequently arranged in lymphoid aggregates. Immunohistochemically, the lesions were positive for vimentin (7/7), smooth muscle actin (8/8), muscle-specific actin (5/7), cytokeratins AE1/AE3 (6/7), and CAM 5.2 (1/7), and antigen CD68 (1/7). No case (0/8) reacted positively with antibody to CD117 (c-kit). Genetically no substitutions, deletions, or insertions occurred in exon 11 in all analyzed samples. Likewise, no deletions or insertions in part of exon 9 were observed. Ultrastructurally the tumor cells revealed features typical of myofibroblasts. According to the morphologic, immunohistochemical, and ultrastructural features mentioned above, especially to the positivity of low-molecular-weight cytokeratins, we propose this lesion to be related to a proliferation of multipotential subserosal cells rather than ordinary myofibroblasts or fibroblasts.
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KIT activation is a ubiquitous feature of gastrointestinal stromal tumors.
Brian P. Rubin, Samuel Singer, C. Tsao et al. · PubMed · 2001 · 969 citations
Jerzy Lasota, Marek Jasiński, Maarit Sarlomo‐Rikala et al. · American Journal Of Pathology · 1999 · 550 citations