Pham Minh Duc, Nguyen Minh Thao, Pham Ngoc Trinh Thi
Department of Surgery, Hue University of Medicine and Pharmacy, Hue University, Hue City, Viet Nam.
Anatomy and Surgical Training Department, Hue University of Medicine and Pharmacy, Hue University, Hue City, Viet Nam.
Ann Med Surg (Lond). 2021 Oct 30;71:102973. doi: 10.1016/j.amsu.2021.102973. eCollection 2021 Nov.
Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue, also called MALT lymphoma, is one of the entities of marginal zone lymphomas. These lymphomas are originated from indolent B-cell lymphomas and involve many organs such as the gastrointestinal tract, salivary gland, skin, lung, thyroid or breast. Ileal MALT lymphoma is relatively rare and clinical symptoms are usually atypical.
We report a case of a 99-year-old man who admitted to the emergency department with increasing and colicky periumbilical pain, vomiting and constipation. Non-contrast-enhanced computed tomography suggested small bowel obstruction due to phytobezoar. Intraoperatively, surgeon discovered the tumor at the site of phytobezoar. Histologically, there was a diffuse infiltration comprised of small to medium sized lymphocytes with monocytoid features. Immunohistochemical result confirmed CD20 positive B-lymphocytes and the Ki-67 proliferation index was 10%. Ileal mucosa-associated lymphoid tissue lymphoma was diagnosed based on histological findings and immunohistochemistry.
MALToma of the gastrointestinal tract is related to chronic antigenic, inflammatory bowel disease and malabsorption syndromes. However, the etiology of ileal MALToma is unclear. Moreover, symptom of ileal MALToma is really not typical and overleaped in the context of small intestinal obstruction. It should be differentiated small intestinal MALToma from immunoproliferative small intestinal disease and an alpha heavy chain disease.
Ileal MALT lymphoma remains little known in many previous studies. It is really difficult to preoperatively diagnose. The combination of clinical presentation, postoperative histology and immunohistochemistry contribute to diagnosis and carry out appropriate management.
黏膜相关淋巴组织结外边缘区淋巴瘤,也称为MALT淋巴瘤,是边缘区淋巴瘤的一种类型。这些淋巴瘤起源于惰性B细胞淋巴瘤,可累及许多器官,如胃肠道、唾液腺、皮肤、肺、甲状腺或乳腺。回肠MALT淋巴瘤相对罕见,临床症状通常不典型。
我们报告一例99岁男性患者,因脐周疼痛加剧、绞痛、呕吐和便秘入住急诊科。非增强计算机断层扫描提示因植物性粪石导致小肠梗阻。术中,外科医生在植物性粪石部位发现肿瘤。组织学检查显示,有由具有单核样特征的中小淋巴细胞组成的弥漫性浸润。免疫组化结果证实为CD20阳性B淋巴细胞,Ki-67增殖指数为10%。根据组织学检查结果和免疫组化诊断为回肠黏膜相关淋巴组织淋巴瘤。
胃肠道MALToma与慢性抗原性、炎症性肠病和吸收不良综合征有关。然而,回肠MALToma的病因尚不清楚。此外,回肠MALToma的症状确实不典型,在小肠梗阻的情况下易被漏诊。应将小肠MALToma与免疫增殖性小肠疾病和α重链病相鉴别。
在许多先前的研究中,回肠MALT淋巴瘤仍鲜为人知。术前诊断确实困难。临床表现、术后组织学检查和免疫组化相结合有助于诊断并进行适当的处理。