Salgado-Sánchez Ernesto, Flores-Flores Jesús, Pérez-Toriz Mario U, Pérez-Cruz Raymundo, Salgado-Sánchez Jesús
Departmento de Cirugía, Hospital de la Sociedad Española de Beneficencia de Puebla, Puebla, México.
Rev Gastroenterol Mex. 2003 Jul-Sep;68(3):219-21.
Our objective was to present a case of inflammatory myofibroblastic tumor of the colon.
Inflammatory myofibroblastic tumors are uncommon. They originate from soft tissues, their appearance is more frequent in childhood and your adulthood and these tumors are composed of myofibroblastic cells, leukocytes, and plasmatic cells. More frequently, these tumors originate in lungs, mesentery, liver and spleen; intestinal appearance is uncommon.
In a 42 year-old male with a lump in right iliac fossa, a colonic inflammatory myofibroblastic tumor infiltrating ileocecal valve was found. Right hemicolectomy was performed. After a 10-month follow-up, no complications were found and no adjuvant therapy was needed.
Inflammatory myofibroblastic tumors have been well described, but, experience is quite limited; Symptoms are consequences of compressed organs in the vicinity. At present, no early detection devices are available, but genetical evaluations for the patient's family members may contribute to unravel a pattern of transmission of the disease.
我们的目的是呈现一例结肠炎性肌纤维母细胞瘤病例。
炎性肌纤维母细胞瘤并不常见。它们起源于软组织,在儿童期和成年期更常见,这些肿瘤由肌纤维母细胞、白细胞和浆细胞组成。这些肿瘤更常起源于肺、肠系膜、肝脏和脾脏;肠道出现的情况并不常见。
在一名42岁右髂窝有肿块的男性患者中,发现了一例浸润回盲瓣的结肠炎性肌纤维母细胞瘤。进行了右半结肠切除术。经过10个月的随访,未发现并发症,也无需辅助治疗。
炎性肌纤维母细胞瘤已有详细描述,但经验相当有限;症状是附近器官受压的结果。目前尚无早期检测手段,但对患者家庭成员进行基因评估可能有助于揭示该疾病的遗传模式。