Amita K, Suma M N, Shankar S Vijay, Premalata C S, Sanjay M
Department of Pathology, Adichunchanagiri Institute of Medical Sciences, Mandya, Karnataka, India.
Department of Pathology, Kidwai Cancer Institute, Bengaluru, Karnataka, India.
Indian J Pathol Microbiol. 2018 Jul-Sep;61(3):446-449. doi: 10.4103/IJPM.IJPM_126_17.
Primary follicular lymphoma (PFL) of gastrointestinal tract (GIT) is rare and account for 1%-3% of non-Hodgkin lymphoma. Within the small intestine, the PFL is more common in jejunum than in the ileum. Due to low prevalence of the disease, the clinical manifestations are not well known, and diagnosis is usually delayed leading to complications. We herein report a case of PFL of GIT who presented with intestinal obstruction and unique gross morphology. Diagnosis was made by morphology and supported by immunohistochemistry.
胃肠道原发性滤泡性淋巴瘤（PFL）较为罕见，占非霍奇金淋巴瘤的1%-3%。在小肠中，PFL在空肠比在回肠更常见。由于该疾病发病率低，其临床表现尚不为人所知，诊断通常会延迟，从而导致并发症。我们在此报告一例胃肠道PFL患者，该患者表现为肠梗阻及独特的大体形态。通过形态学诊断，并得到免疫组织化学的支持。
