مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

MULTIPLE GRANULAR CELL TUMOR IN A TEENAGER: REPORT OF A CASE AND REVIEW OF THE LITERATURE

Pages

  228-231

Abstract

 Granular cell tumors are rare neoplasms of uncertain histogenesis but with a typicalhistologic appearance composed of cells with characteristic granular cytoplasm. These tumors occur most often in adults as an asymptomatic solitary papule or nodule. MULTIPLE granular cell tumors are rare, especially in children and teenagers. We represent a case of MULTIPLE granular cell tumors in a 19-year-old girl presented with MULTIPLE cutaneous and mucosal nodular lesions. The diagnosis was documented by histopathology and IMMUNOHISTOCHEMISTRY

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    Cite

    APA: Copy

    GOLCHAI, J., ZARGARI, O., & PAKNEJADI, M.B.. (2004). MULTIPLE GRANULAR CELL TUMOR IN A TEENAGER: REPORT OF A CASE AND REVIEW OF THE LITERATURE. ACTA MEDICA IRANICA, 42(3), 228-231. SID. https://sid.ir/paper/277599/en

    Vancouver: Copy

    GOLCHAI J., ZARGARI O., PAKNEJADI M.B.. MULTIPLE GRANULAR CELL TUMOR IN A TEENAGER: REPORT OF A CASE AND REVIEW OF THE LITERATURE. ACTA MEDICA IRANICA[Internet]. 2004;42(3):228-231. Available from: https://sid.ir/paper/277599/en

    IEEE: Copy

    J. GOLCHAI, O. ZARGARI, and M.B. PAKNEJADI, “MULTIPLE GRANULAR CELL TUMOR IN A TEENAGER: REPORT OF A CASE AND REVIEW OF THE LITERATURE,” ACTA MEDICA IRANICA, vol. 42, no. 3, pp. 228–231, 2004, [Online]. Available: https://sid.ir/paper/277599/en

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