ABSTRACT: The gastrointestinal stromal tumors (GIST) are rare and consist in mesenchymal neoplasms of the gastrointestinal tract, which may affect any part of the gastrointestinal tract, and is more frequent in stomach. We report a case of a 65-years-old male patient who presented a mass in the proximal ileum found by exploratory laparotomy. The patient underwent a segmental enterectomy with total resection of the tumor and free surgical margins with the pathological diagnosis of GIST, confirmed by immunohistochemistry (CD117).
Key words: ileumileum,gastrointestinal stromal tumorgastrointestinal stromal tumor,small intestine tumorsmall intestine tumor.
RESUMEN: Los tumores del estroma gastrointestinal (GIST) son raros, consisten en neoplasias de origen mesodérmico del tracto gastrointestinal y pueden acometer cualquier parte del tracto gastrointestinal, siendo más frecuentes en el estómago. Reportamos el caso de un paciente varón, de 65 años de edad, con una masa en el íleon proximal, descubierta mediante laparotomía exploratoria. Se ha realizado una enterectomía segmentaria, con la resección total del tumor y márgenes quirúrgicos libres. El diagnóstico anatomopatológico de GIST fue confirmado por inmunohistoquímica (CD117).
Palabras clave: íleon, tumor del estroma gastrointestinal, tumor del intestino delgado.
RESUMO: Os tumores estromais gastrointestinais (GISTs) são raros, consistem em neoplasias mesenquimais do trato gastrointestinal e podem acometer qualquer parte do trato gastrointestinal, sendo mais frequentes no estômago. Relatamos o caso de um paciente do sexo masculino, 65 anos de idade, com uma massa em íleo proximal, descoberta em uma laparotomia exploradora. Foi realizada enterectomia segmentar com ressecção total do tumor e margens cirúrgicas livres, com o diagnóstico anatomopatológico de GIST confirmado por imuno-histoquímica (CD117).
Unitermos: íleo, tumor estromal gastrointestinal, tumor de intestino delgado.
CASE REPORT
Giant gastrointestinal stromal tumor of the proximal ileum
Tumor estromal gastrointestinal gigante do íleo proximal
Received: 29 March 2019
Revised document received: 03 April 2019
Accepted: 03 April 2019
Published: 20 August 2019
Gastrointestinal stromal tumors (GIST) are rare and account for about 1% of gastrointestinal tumors(1), which can affect any part of the gastrointestinal tract, and are more frequent in the stomach(2), predominantly in the age group 50-60 years(3), with no prevalence between men and women(2). Such tumors present mesenchymal origin in the interstitial cells of Cajal(2, 4).
A 65-year-old male patient presented a mass in the proximal ileum found during exploratory laparotomy. Tumor resection was performed with free surgical margins; the material was submitted to pathological anatomy examination whose macroscopy revealed a tumor lesion measuring 13.5 × 13 × 8.5 cm, and sections showed a cystic lesion with a white solid area and a necrotic component in the wall, draining hemorrhagic fluid (Figure 1). Microscopy revealed a tumor with spindle cells, elongate nuclei, abundant cytoplasm, marked congestion and necrosis (Figure 2). The anatomopathological diagnosis was GIST, confirmed by immunohistochemistry (CD117).


HE: hematoxylin and eosin.
GISTs are considered rare tumors when compared to other gastrointestinal tumors. However, they are the most common type among mesenchymal tumors of the gastrointestinal tract. Immunohistochemistry by CD117 confirms the diagnosis. Complete surgical resection of the lesion with safety margin is the main curative approach for patients with primary tumors; however, Imatinib chemotherapy is also used depending on patient’s clinical conditions(1,5).
CORRESPONDING AUTHOR: Kelen Christina Alves Bezzerra, 0000-0001-7914-432X. e-mail: drpatologia@hospitalsaofrancisco.com


HE: hematoxylin and eosin.