Smith Brandon M, Reilly Kyle, Baker Elena, Deeken Amy, Dan Adrian G
Department of Surgery, Akron City Hospital Summa Health, Akron, OH, USA; Northeast Ohio Medical University, Rootstown, OH, USA.
Int J Surg Case Rep. 2020;69:28-31. doi: 10.1016/j.ijscr.2020.03.022. Epub 2020 Mar 28.
Mantle Cell Lymphoma (MCL) is a non-Hodgkin lymphoma accounting for 2.5% of lymphoid neoplasms in the United States. Primary gastrointestinal (GI) lymphomas account for 1-4% of all GI malignancies, with few reports of primary mantle cell lymphoma presenting as a single colonic mass and none to our knowledge with colon-colonic intussusception as the presenting finding. Accurate and timely diagnosis is imperative because MCL has rapid progression and early chemotherapeutic intervention results in improved patient outcomes. This work is reported in line with the SCARE criteria [1] for case report publication.
A 61-year-old male presented with 1 month history of nonspecific right sided abdominal pain. Computed Tomography (CT) of the abdomen identified an intussuscepting mass in the proximal ascending colon and an additional 8 mm hepatic lesion. Colonoscopy identified a large mass in the corresponding area of colon identified on CT. Histology and immunohistochemistry of biopsied specimen diagnosed MCL.
Planned surgical intervention was deferred and the patient was referred for oncologic treatment. We report the first case to our knowledge of MCL presenting as colon-colonic intussusception and discuss the work-up of this rare lymphoma that clinicians may be required to diagnose and manage.
This report serves as a reminder to maintain a broad differential inclusive of uncommon diseases and unanticipated pathology. Practicing with a thorough understanding of medical principles and clinical acumen is essential for optimal patient care and, as demonstrated in this case, preventing a potentially unnecessary surgical intervention thus delaying appropriate chemotherapy.
套细胞淋巴瘤(MCL)是一种非霍奇金淋巴瘤,占美国淋巴肿瘤的2.5%。原发性胃肠道(GI)淋巴瘤占所有GI恶性肿瘤的1 - 4%,很少有原发性套细胞淋巴瘤表现为单个结肠肿块的报道,据我们所知,尚无以结肠 - 结肠套叠为首发表现的病例。准确及时的诊断至关重要,因为MCL进展迅速,早期化疗干预可改善患者预后。本病例报告符合病例报告发表的SCARE标准[1]。
一名61岁男性,有1个月的右侧腹部非特异性疼痛病史。腹部计算机断层扫描(CT)发现升结肠近端有一个套叠肿块以及一个8毫米的肝脏病变。结肠镜检查在CT所示的结肠相应区域发现一个大肿块。活检标本的组织学和免疫组织化学诊断为MCL。
原计划的手术干预推迟,患者被转诊接受肿瘤治疗。据我们所知,我们报告了首例以结肠 - 结肠套叠形式出现的MCL病例,并讨论了这种罕见淋巴瘤的检查方法,临床医生可能需要对其进行诊断和管理。
本报告提醒我们要保持广泛的鉴别诊断,包括罕见疾病和意外病理情况。全面理解医学原理并具备临床敏锐度对于提供最佳患者护理至关重要,如此病例所示,可避免潜在的不必要手术干预,从而延迟适当的化疗。