Cover image of the article: Inflammatory Myofibroblastic Tumor of saplinx: a very rare case treated with a less aggressive method

Image Credit:Int J Cancer Manag

Inflammatory Myofibroblastic Tumor of saplinx: a very rare case treated with a less aggressive method

Authors

Fatemeh Homaei-Shandiz1, Reza Jafarzadeh-Esfehani2, Nasrin Moazzen3, Amir Amirabadi4,*
1Associated Professor of Radiation Oncology, Solid tumors Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
2Medical Student, Sabzevar University of Medical Sciences, Sabzevar, Iran
3Fellow of Allergy and Clinical Immunology, Mashhad University of Medical Sciences, Mashhad, Iran
4Radiation Oncologist, Solid tumors Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
*Corresponding Author: Corresponding author: Amir Amirabadi, Radiation Oncologist, Solid tumors Research Center, Mashhad University of Medical Sciences, Mashhad, Iran, Tel: +98-5115224472, E-mail: Email: amirabadia871@mums.ac.ir

International Journal of Cancer Management:Vol. 7, issue 4; e80565
Published online:Dec 31, 2014
Article type:Case Report
Received:Apr 25, 2014
Accepted:Jun 22, 2014
How to Cite:Homaei-Shandiz F, Jafarzadeh-Esfehani R, Moazzen N, Amirabadi A. Inflammatory Myofibroblastic Tumor of saplinx: a very rare case treated with a less aggressive method. Int J Cancer Manag. 2014;7(4):e80565. doi:

Abstract

Inflammatory pseudotumour describes as a wide range of neoplastic and reactive lesions. One of the rare presentations of these tumors is found in the salpinx. This case report characterizes a thirty six year old woman with a history of left sided abdominal pain for a few months. Further examinations revealed that she had a complex cyst in her left salpinx. The patient had normal levels of tumor markers such as CA125, Alfa Fetoprotein (AFP), and Human Chorionic Gonadotropin (hCG), while other paraclinical test were in normal values Additionaly The patient underwent left salpingectomy by a gynecologist. The pathological diagnosis of the lesion was inflammatory myofibroblastic tumor (IMT). In immunohistochemistry the tumor stains was moderately positive in anaplastic lymphoma kinase (ALK) and also actin positive. Total resection of tumor was performed with no complications and remained disease free during follow up for 40 months. Although Inflammatory Myofibroblastic Tumor (IMT) is benign in nature, but in order to improve the prognosis, this tumor requires low intensity surgical treatment.

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Copyright

© 2014, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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