首页> 外文期刊>International Journal of Surgery Case Reports >Duodeno-colic fistula as a rare presentation of lung cancer - surgical treatment of a stage IV oligometastatic lung disease
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Duodeno-colic fistula as a rare presentation of lung cancer - surgical treatment of a stage IV oligometastatic lung disease

机译:十二指肠结肠瘘是肺癌的罕见表现-IV期少转移性肺疾病的手术治疗

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Introduction: Rare adenosquamous carcinomas have no defined standard approach given their low incidence. They present with nonspecific imaging characteristics and are described as having worse prognosis than other lung malignancies, with greater likelihood of local invasion and early metastasis. Presentation of case: Male caucasian patient, 43 years, 26 pack-year smoking history, presented with watery diarrhea, early emesis and loss of 25% body weight (20kg) in four weeks. Colonoscopy identified a left colonic mass. Abdominal CT/ultrasound showed a large fistulous lesion between the 4th portion of the duodenum and left colon. CT showed a solid mass in the right upper lung lobe. Endoscopy and transthoracic biopsy were inconclusive. En bloc D3 and D4 duodenectomy, proximal enterectomy and left hemicolectomy were performed, with inconclusive histology of the specimen. Three months later, a right upper lung lobectomy with lymphadenectomy was performed, revealing an adenosquamous carcinoma of lung origin, R0, staged as pT2pN0pM1b. Six months later, a single dural metastasis in the left cerebellopontine angle was detected and resected, with subsequent holocranial radiotherapy and systemic adjuvant chemotherapy. Patient is currently with 18 months follow-up, in good general health and with no evidence of recurrent disease. Discussion: There are no specific guidelines to treat oligometastatic adenosquamous lung carcinoma. Our approach was abdominal surgery as a life-saving procedure and, months later, oncological resection of primary lung tumor and metachronous metastasis to the brain. Conclusion: A systematic, patient-oriented, patient-shared, multidisciplinary approach is particularly relevant when dealing with atypical presentations of rare diseases in young patients.
机译:简介:罕见的腺鳞癌由于其发病率较低,因此没有明确的标准方法。它们表现出非特异性的影像学特征,并被描述为比其他肺恶性肿瘤的预后更差,更有可能发生局部浸润和早期转移。病例介绍:男性白人患者,年龄43岁,吸烟史26包年,出现水样腹泻,早期呕吐,四周内体重减轻25%(20公斤)。结肠镜检查发现左结肠肿块。腹部CT /超声检查显示十二指肠第四部分和左结肠之间有较大的瘘管病变。 CT显示右上肺叶有实性肿块。内镜检查和经胸活检尚无定论。进行整体D3和D4十二指肠切除术,近端肠切除术和左半结肠切除术,标本组织学尚无定论。三个月后,进行了右上肺叶切除和淋巴结清扫术,发现肺源性腺鳞癌R0分期为pT2pN0pM1b。六个月后,发现并切除了左小脑桥角的单个硬脑膜转移,随后进行了全颅放疗和全身辅助化疗。该患者目前正在接受18个月的随访,总体健康状况良好,没有复发疾病的迹象。讨论:目前尚无治疗低转移性腺鳞癌的具体指南。我们的方法是进行挽救生命的腹部手术,几个月后,肿瘤切除了原发性肺肿瘤并转移到了大脑。结论:当处理年轻患者中罕见疾病的非典型表现时,系统的,以患者为中心,患者共享的多学科方法尤为重要。

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