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À§ °£ÁúÁ¾¾çÀÇ ºÐ·ù ¹× ÀÓ»óÀû °íÂû Classification and Clinical Evaluation of Gastrointestinal Stromal Tumor -Immunohistochemical Expression of CD117, CD34, ¥á-Smooth Muscle Actin, S-100 -

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±ÇÇõ¿ì/Kwon HW ·ù½Â¿Ï/±èÀÎÈ£/±Ç°Ç¿µ/¼Õ¼ö»ó/Ryu SW/Kim IH/Kwon KY/Sohn SS

Abstract


Purpose: Gastrointestinal stromal tumors (GISTs) represent a distinct and the most important subset of, mesenchymal tumors of the GI tract. Stromal tumors of the gastrointestinal tract have long been a source of confusion and controversy, with regard to their classification, differentiation, criteria of malignancy and prognostic features.
Methods: The 26 case studies of patients treated for a Gastrointestinal mesenchymal tumor, including leiomyomas, leiomyosarcomas and GISTs, between 1994 and 2002 at Keimyung University Hospital, were evaluated retrospectively. The cases were confirmed as leiomyomas, schwannomas, or GISTs by pathological re-examination. 20 of the cases were diagnosed as GISTs, from the pathological examination, and were chosen for the evaluation of their clinicopathological and immunohistochemical characteristics, using CD34, CD117, ¥á-SMA and S-100 done.
Results: The new diagnoses of the mesenchymal tumors were a leiomyoma in 3 cases, a schwannoma in 3 and gastric stromal tumors in all 20. The immunohistochemical studies were positive for CD117 and CD34 in 95 and 75% of the gastric stromal tumors, respectively. The histopathological findings showed 5 benign tumors, 3 borderline tumors, and 12 malignant tumors in the 20 patients.
Conclusion: The immunohistochemical marker (CD117) for KIT is a specific marker for GISTs among the tumors occurring in the stomach, and can be used to distinguish GISTs from true leiomyomas and gastric schwannomas. We also found that severe cellularity, atypism, intramoral hemorrhage and necrosis, large size and a high mitotic count correlate with malignant behaviour and a poor prognosis.

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