Published online Jan 6, 2020. doi: 10.12998/wjcc.v8.i1.234
Peer-review started: October 22, 2019
First decision: November 11, 2019
Revised: November 14, 2019
Accepted: November 27, 2019
Article in press: November 27, 2019
Published online: January 6, 2020
Processing time: 77 Days and 0.3 Hours
Primary intestinal extranodal natural killer/T-cell lymphoma, nasal type (PI-ENKTCL) is a rare non-Hodgkin’s lymphoma (NHL) subtype, and its prognosis is extremely poor. Clinical characteristics of the disease are not obvious and easily misdiagnosed. In this case report, we describe a patient with PI-ENKTCL who presented with intermittent hematochezia. The advantages of positron emission tomography/computed tomography (PET-CT) as a useful diagnostic tool and the role of surgery as an important therapy are highlighted.
A 45-year-old man, hospitalized due to intermittent hematochezia, underwent gastroscopy, colonoscopy, biopsy and CT, but no cause was found. Hence, we carried out a multidisciplinary team (MDT) discussion on the causes and treatment of this patient, and it was decided to perform PET-CT imaging with a MDT discussion of the results. PET-CT demonstrated a diagnosis of lymphoma and it was decided to surgically resect the lesion, and a R0 resection was successfully performed. Postoperative pathology showed negative resection margins, and examination of the lesion confirmed the diagnosis of PI-ENKTCL. After surgery, the patient underwent a follow-up period of 6 mo and received 6 cycles of gemcitabine, oxaliplatin and L-asparaginase. No recurrence or metastasis occurred.
PI-ENKTCL is rare, and MDT discussion is required during diagnosis. PET-CT can be performed for imaging diagnosis. Treatment is based on surgical resection, and the best treatment regimen is determined according to postoperative pathological results to improve prognosis and to extend survival in patients.
Core tip: Primary intestinal extranodal natural killer/T-cell lymphoma, nasal type (PI-ENKTCL) is a very rare disease and its prognosis is extremely poor. Due to its rarity, PI-ENKTCL has not been thoroughly investigated. Moreover, knowledge of its clinical characteristics is limited. Hence, we report a patient with PI-ENKTCL and review the corresponding literature to improve our knowledge of this disease and avoid misdiagnosis.