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Information Journal Paper

Title

PLEXIFORM ANGIOMYXOID MYOFIBROBLASTIC TUMOR IN A 38 YEARS OLD MAN (CASE REPORT)

Pages

  98-100

Abstract

PLEXIFORM ANGIOMYXOID MYOFIBROBLASTIC TUMOR is a very rare mesenchymal tumor of STOMACH which is diagnosed based on morphologic findings such as plexiform growth pattern, spindle cell proliferation in a myxoid background, by aiding immunohistochemistry staining and ruling out of other mesenchymal gastric tumors. We report this tumor with about 4cm size in antrum of a 38 years old man which endoscopic and CT scan results fit with GASTROINTESTINAL STROMAL TUMOR and diagnoses is performed according to specific morphologic and immunohistochemistry findings.

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  • Cite

    APA: Copy

    SAFAEI, AKBAR, VAHEDI, AMIR, & VAHEDI, LEILA. (2018). PLEXIFORM ANGIOMYXOID MYOFIBROBLASTIC TUMOR IN A 38 YEARS OLD MAN (CASE REPORT). MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, 40(1 ), 98-100. SID. https://sid.ir/paper/46899/en

    Vancouver: Copy

    SAFAEI AKBAR, VAHEDI AMIR, VAHEDI LEILA. PLEXIFORM ANGIOMYXOID MYOFIBROBLASTIC TUMOR IN A 38 YEARS OLD MAN (CASE REPORT). MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2018;40(1 ):98-100. Available from: https://sid.ir/paper/46899/en

    IEEE: Copy

    AKBAR SAFAEI, AMIR VAHEDI, and LEILA VAHEDI, “PLEXIFORM ANGIOMYXOID MYOFIBROBLASTIC TUMOR IN A 38 YEARS OLD MAN (CASE REPORT),” MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, vol. 40, no. 1 , pp. 98–100, 2018, [Online]. Available: https://sid.ir/paper/46899/en

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