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Occult Non-small Cell Lung Cancer Presenting as Paraneoplastic Gastroparesis: A Case Report and Literature Review

机译:隐匿性非小细胞肺癌表现为副肿瘤性胃轻瘫:一例报道并文献复习

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Paraneoplastic gastrointestinal syndromes rarely precede the actual detection of an overt cancer with gastroparesis being a very rare initial presentation. To increase the clinical awareness of this rare clinical entity, we present a case of severe gastroparesis that was later proven to be associated with an occult poorly differentiated non-small cell lung cancer.?We then continue to briefly review the relevant literature on paraneoplastic gastrointestinal syndromes to date. A 61-year-old African-American man presented with two months history of severe post-prandial nausea, vomiting and bloating associated with unintentional weight loss of 20 pounds. General physical examination revealed cachexia, temporal muscle wasting and clubbing of nails in both hands. The following investigations were normal or negative: basic metabolic panel, liver function tests, chest X-ray and esophagogastroduodenoscopy. Computed tomography (CT) scan of the abdomen showed residual food in the stomach and scintigraphic gastric emptying studies were consistent with gastroparesis. CT scan of the chest was performed which revealed a spiculated nodule sized 9 mm?in right upper lobe of the lung with right hilar lymphadenopathy. Positron emission tomography (PET) scan revealed hyper-metabolic activity in the right upper lobe nodule and right hilar adenopathy. Nodule resection and biopsy revealed a poorly differentiated non-small cell lung carcinoma. Due to the concern of paraneoplastic origin of his gastroparesis further serological testing showed positive anti-neuronal nuclear antibodies type 1 (Anti-Hu) and cytoplasmic purkinje cell antibodies (Anti-Yo). The patient was started on a chemotherapy combination of Carboplatin and Paclitaxel with a three-week course of local radiation therapy. Moreover, for the relief of his severe gastrointestinal (GI) symptoms dietary modifications, pro-kinetic agents and psychological counseling were used with gradual clinical improvement observed on follow-up visits.
机译:副肿瘤胃肠综合征很少在实际发现明显癌症之前发生,而胃轻瘫是非常罕见的初始表现。为了提高对这种罕见临床实体的临床认识,我们介绍了一例严重的胃轻瘫,后来被证实与隐匿性低分化非小细胞肺癌有关。然后我们继续简要回顾有关副肿瘤胃肠道的相关文献。迄今为止的综合症。一名61岁的非洲裔美国人,有两个月的严重餐后恶心,呕吐和腹胀史,并意外体重减轻了20磅。常规体格检查发现恶病质,颞部肌肉消瘦和两只手的指甲杵状。以下检查为正常或阴性:基本代谢检查,肝功能检查,胸部X线检查和食管胃十二指肠镜检查。腹部计算机断层扫描(CT)扫描显示胃中残留食物,闪烁显像胃排空研究与胃轻瘫相符。胸部CT扫描显示肺右上叶有一个大小为9 mm?的小结节,并伴有右肺门淋巴结肿大。正电子发射断层扫描(PET)扫描显示右上叶结节和右肺门腺病的代谢活跃。结节切除和活检显示低分化的非小细胞肺癌。由于担心他胃轻瘫的副肿瘤起源,进一步的血清学检查显示阳性的1型抗神经元核抗体(Anti-Hu)和胞质浦肯野细胞抗体(Anti-Yo)。该患者开始接受卡铂和紫杉醇的化学疗法联合治疗,疗程为三周。此外,为缓解他的严重胃肠道症状,饮食调整,促动剂和心理咨询被采用,并在随访中观察到临床逐渐改善。

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