Freeman H J, Chiu B K
Gastroenterology. 1986 Jun;90(6):2008-12. doi: 10.1016/0016-5085(86)90275-1.
Malignant small intestinal lymphoma may complicate or antedate clinical recognition of celiac sprue. However, histologic diagnosis of lymphoma is made especially difficult in the presence of small bowel ulceration. A 70-yr-old man with celiac sprue and a history of dermatitis herpetiformis was initially seen for recurrent diarrhea; panmalabsorption with steatorrhea and protein-losing enteropathy were documented. Subsequent studies showed ectopic gastric mucosa in the small bowel, hyposplenism with mesenteric lymph node cavitation, and small bowel erosions and ulceration. Despite strong clinical suspicion for more than 2 yr, only 1 of 88 small bowel biopsy specimens was positive for lymphoma. At autopsy, shortly after histologic diagnosis of lymphoma, extensive small bowel involvement and infiltration were observed. This is the first report of lymphoma complicating the recently described nonneoplastic lymphoreticular syndrome associated with celiac sprue characterized by splenic atrophy and mesenteric lymph node cavitation.
恶性小肠淋巴瘤可能使乳糜泻的临床诊断复杂化或早于其出现。然而,在存在小肠溃疡的情况下,淋巴瘤的组织学诊断尤其困难。一名70岁患有乳糜泻且有疱疹样皮炎病史的男性最初因反复腹泻就诊;记录显示存在脂肪泻和蛋白质丢失性肠病导致的全吸收不良。随后的研究显示小肠中有异位胃黏膜、脾功能减退伴肠系膜淋巴结空洞形成以及小肠糜烂和溃疡。尽管临床高度怀疑超过2年,但88份小肠活检标本中只有1份淋巴瘤呈阳性。尸检时,在淋巴瘤组织学诊断后不久,观察到小肠广泛受累和浸润。这是关于淋巴瘤并发最近描述的与乳糜泻相关的非肿瘤性淋巴网状综合征(其特征为脾萎缩和肠系膜淋巴结空洞形成)的首例报告。