Mashayekhi Azin, Quiroga Eleonora Fiorletta, Margolick Joseph F, Post Ginell R
Department of Pathology University of Arkansas for Medical Sciences Little Rock Arkansas USA.
Division of Trauma and Surgical Critical Care Department of Surgery University of Arkansas for Medical Sciences Little Rock Arkansas USA.
Clin Case Rep. 2022 Mar 6;10(3):e05546. doi: 10.1002/ccr3.5546. eCollection 2022 Mar.
Primary gastrointestinal T-cell lymphomas are rare. Presenting symptoms can be non-specific, and imaging studies can show overlap with nonmalignant processes. Definitive diagnosis requires clinical suspicion and histologic evaluation with ancillary studies for appropriate disease classification and therapeutic intervention.
原发性胃肠道T细胞淋巴瘤很罕见。其临床表现可能不具有特异性,影像学检查结果可能与非恶性病变重叠。明确诊断需要临床怀疑,并通过辅助检查进行组织学评估,以实现恰当的疾病分类和治疗干预。