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Inflammatory myofibroblastic tumor of salpinx: a very rare case treated with a less aggressive method.
Homaei-Shandiz, Fatemeh; Jafarzadeh-Esfehani, Reza; Moazzen, Nasrin; Amirabadi, Amir.
Afiliação
  • Homaei-Shandiz F; Associated Professor of Radiation Oncology, Solid tumors Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Jafarzadeh-Esfehani R; Medical Student, Sabzevar University of Medical Sciences, Sabzevar, Iran.
  • Moazzen N; Fellow of Allergy and Clinical Immunology, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Amirabadi A; Radiation Oncologist, Solid tumors Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Iran J Cancer Prev ; 7(4): 244-7, 2014.
Article em En | MEDLINE | ID: mdl-25628846
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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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2014 Tipo de documento: Article