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Primary gastric inflammatory myofibroblastic tumor: A case report

RATIONALE: Primary gastric inflammatory myofibroblastic tumor is extremely rare. Only a few cases were reported in the domestic and foreign medical literature with corresponding imaging findings of this disease even more rarely reported. PATIENT CONCERNS: We present one case of a 52-year-old female...

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Detalles Bibliográficos
Autores principales: Cheng, Bingxue, Yang, Chen, Liu, Zhou, Liu, Lijian, Zhou, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320093/
https://www.ncbi.nlm.nih.gov/pubmed/30557996
http://dx.doi.org/10.1097/MD.0000000000013423
Descripción
Sumario:RATIONALE: Primary gastric inflammatory myofibroblastic tumor is extremely rare. Only a few cases were reported in the domestic and foreign medical literature with corresponding imaging findings of this disease even more rarely reported. PATIENT CONCERNS: We present one case of a 52-year-old female patient with upper abdominal pain, acid reflux, and belching for 2 months. DIAGNOSES AND INTERVENTIONS: Electron ultrasound gastroscopy (EUS) revealed elevation of gastric antrum mucosa. A whole abdominal and pelvic multi-slice spiral computed tomography (CT) detected a round nodule in the gastric antrum with considerably delayed enhancement, with initial suspicion of gastrointestinal stromal tumors (GISTS). Then a laparoscopic assisted distal gastrectomy was performed. Finally, the postoperative pathology confirmed the diagnosis of primary gastric IMT. OUTCOMES: After 6 months of follow-up, the patient was still alive without any evidence of metastasis or recurrence. LESSONS: Familiarizing with the CT features of this rare tumor may raise radiologists’ awareness of the disease and potentially could avoid misdiagnosis.