Shrestha Bikram, Kim Bernard, Huffstetler Alison
Department of Internal Medicine, Saint Agnes Hospital Center, Baltimore, MD, USA;
Department of Critical Care and Pulmonary Medicine, Saint Agnes Hospital Center, Baltimore, MD, USA.
J Community Hosp Intern Med Perspect. 2016 Sep 7;6(4):31707. doi: 10.3402/jchimp.v6.31707. eCollection 2016.
Mucosa-associated lymphoid tissue (MALT)-type lymphoma is a relatively rare disease; nevertheless, it is the third most common lymphoma type, accounting for 5-7% of all non-Hodgkin lymphomas. Case series and retrospective analysis published in the literature have suggested that extra gastrointestinal (GI) MALT-type lymphoma can occur simultaneously with MALT-type lymphoma involving the GI tract. We report the case of a healthy, 64-year-old Caucasian male who presented with progressive fatigue, non-productive cough, and worsening exertional shortness of breath for 3 months who was subsequently diagnosed with gastric extra-nodal marginal zone B-cell lymphoma or MALToma with simultaneous metastasis to the lung (bronchi) based on biopsy reports.
A 64-year-old Caucasian male presented to the emergency room complaining of progressive fatigue for 3 months which had progressed to the point of hindering his usual activities of daily living (ADL). He had recently visited his primary care provider for evaluation of a non-productive cough and exertional shortness of breath. A chest radiography obtained at the time showed bilateral infiltrates. He was then treated for atypical pneumonia but his symptoms unfortunately did not improve. Initial investigations in the emergency room revealed severe anemia and a positive stool guaiac test. Imaging showed bilateral pulmonary infiltrates and an irregular gastric mass. Gastric and transbronchial biopsies were suggestive of extra-nodal marginal zone B-cell lymphoma with simultaneous metastasis to the bronchi. He was treated symptomatically with transfusion of packed red blood cells (PRBC) and intravenous iron followed by radiotherapy. Helicobacter pylori infection was ruled out eliminating the possibility of treating him with eradication therapy.
Although the stomach is the most common and most extensively studied site of involvement of MALT lymphomas, they can also emerge in many other locations. MALT lymphomas have a high tendency to disseminate to other sites; therefore, extensive staging may be necessary to look for suspicious lesions.
黏膜相关淋巴组织(MALT)型淋巴瘤是一种相对罕见的疾病;然而,它是第三常见的淋巴瘤类型,占所有非霍奇金淋巴瘤的5 - 7%。文献中发表的病例系列和回顾性分析表明,胃肠道外(GI)MALT型淋巴瘤可与累及胃肠道的MALT型淋巴瘤同时发生。我们报告一例健康的64岁白种男性病例,该患者出现进行性疲劳、干咳和劳力性气短加重3个月,随后根据活检报告被诊断为胃结外边缘区B细胞淋巴瘤或MALToma,并同时转移至肺(支气管)。
一名64岁白种男性因进行性疲劳3个月就诊于急诊室,疲劳已发展到妨碍其日常生活活动(ADL)的程度。他最近因干咳和劳力性气短去看了初级保健医生。当时进行的胸部X线检查显示双侧浸润。他随后接受了非典型肺炎的治疗,但不幸的是症状并未改善。急诊室的初步检查显示严重贫血和大便潜血试验阳性。影像学检查显示双侧肺部浸润和一个不规则的胃部肿块。胃和经支气管活检提示结外边缘区B细胞淋巴瘤并同时转移至支气管。他接受了对症治疗,输注浓缩红细胞(PRBC)和静脉补铁,随后进行了放疗。排除了幽门螺杆菌感染,消除了用根除疗法治疗他的可能性。
尽管胃是MALT淋巴瘤最常见且研究最广泛的受累部位,但它们也可出现在许多其他部位。MALT淋巴瘤有很高的扩散到其他部位的倾向;因此,可能需要进行广泛的分期以寻找可疑病变。