Diagnostic Snapshot: A Patient With Gastrointestinal Symptoms and Eosinophilia
Rashida Taher, S. Kurtin
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引用次数: 0
Abstract
© 2019 Harborside Press® J Adv Pract Oncol 2019;10(2):180–183 HISTORY Mr. C, a 63-year-old Cape Verdean male, was referred to the hematology/oncology office for evaluation of eosinophilia in May 2017. The eosinophilia was first documented in December 2003 by his primary care provider. In March 2005, Mr. C underwent colonoscopy for mild rectal bleeding and was incidentally found to have eosinophilic colitis. Stool ova and parasite testing was negative. Because he was asymptomatic at the time, no treatment was initiated. One year later (2006), Mr. C developed dyspepsia in the presence of continued eosinophilia. An upper endoscopy with biopsy was performed, revealing Helicobacter pylori–positive chronic active gastritis. He was treated with a 14-day course of triple therapy. Follow-up H. pylori antigen stool test was negative. In April 2017, Mr. C developed recurrent abdominal pain for which an endoscopy and colonoscopy were performed. Biopsies of the cecum, splenic flexure, and sigmoid colon were significant for eosinophilic infiltrates. A complete blood count demonstrated eosinophilia with normal hemoglobin, white blood cell, and platelet counts. Stool testing using an extended gastrointestinal panel was unremarkable. It was at this time that Mr. C was referred to hematology/oncology. Past medical history was significant for diabetes, hypertension, and hyperlipidemia. Mr. C did not have a history of asthma or food/drug allergies. His medications included amlodipine at 25 mg, aspirin at 325 mg, glipizide at 5 mg, metformin at 1,000 mg, and pravastatin at 80 mg. A review of systems revealed that Mr. C was negative for any fevers, night sweats, weight loss, rash/pruritus, dyspnea, or diarrhea. A physical exam showed normal vital signs, no palpable adenopathy, normal cardiopulmonary exam, no hepatosplenomegaly, no palpable masses, and no skin rashes or nodules. A computed tomography scan of the chest, abdomen, and pelvis was unremarkable. No adenopathy, masses, or hepatosplenomegaly were noted. Mr. C’s labs are shown in Tables 1 and 2. Th is ar tic le is dis tri bu te d u nd er th e t er m s o f t he Cr ea tiv e C om m on s A ttr ibu tio n N on -C om m er cia l L ice ns e, wh ich pe rm its
诊断快照:一个有胃肠道症状和嗜酸性粒细胞增多的病人
©2019 Harborside Press®J Adv Pract Oncol 2019;10(2):180-183病史C先生,63岁,佛得角男性,于2017年5月被转诊至血液学/肿瘤学办公室进行嗜酸性粒细胞增多症评估。2003年12月,他的初级保健提供者首次记录了嗜酸性粒细胞增多症。2005年3月,C先生因轻度直肠出血接受了结肠镜检查,偶然发现患有嗜酸性结肠炎。粪便卵和寄生虫检测呈阴性。因为他当时没有症状,所以没有开始治疗。一年后(2006年),C先生在持续的嗜酸性粒细胞增多的情况下出现消化不良。进行了带活检的上内镜检查,发现幽门螺杆菌阳性的慢性活动性胃炎。他接受了为期14天的三联治疗。随访幽门螺杆菌抗原粪便检测结果为阴性。2017年4月,C先生出现复发性腹痛,为此进行了内窥镜检查和结肠镜检查。盲肠、脾曲和乙状结肠的活检对嗜酸性粒细胞浸润有重要意义。全血细胞计数显示嗜酸性粒细胞增多,血红蛋白、白细胞和血小板计数正常。使用扩展胃肠道小组进行大便测试并不显著。正是在这个时候,C先生被转诊到血液学/肿瘤学。既往病史对糖尿病、高血压和高脂血症具有重要意义。C先生没有哮喘或食物/药物过敏史。他的药物包括25 mg的氨氯地平、325 mg的阿司匹林、5 mg的格列吡嗪、1000 mg的二甲双胍和80 mg的普伐他汀。系统审查显示,C先生发烧、盗汗、体重减轻、皮疹/瘙痒、呼吸困难或腹泻均为阴性。体检显示生命体征正常,无明显腺病,心肺检查正常,无肝脾肿大,无明显肿块,无皮疹或结节。胸部、腹部和骨盆的计算机断层扫描并不明显。未发现腺病、肿块或肝脾肿大。C先生的实验室如表1和表2所示。这是对Cr ea tive C om m on s A ttr ibu tio n n on-C om m er cia l ice es e的三次分解,其结果是
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