肺肠分化腺癌(PEAC)罕见病例:诊断挑战和治疗考虑

Bipneet Singh , Jahnavi Ethakota , Sakshi Bai , Waryaam Singh , Palak Grover , Gurleen Kaur , Sruthi Ramanan , Merritt Bern
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引用次数: 0

摘要

肠分化腺癌(PEAC)是一种罕见的肺腺癌变体,其特征是肠成分和独特的免疫组织化学标志物。由于其与原发性结直肠腺癌的相似性及其独特的临床表现,该变异在诊断和治疗方面提出了挑战。我们报告一位76岁男性病例,有一个月的呼吸道症状史,最初被诊断为肺炎。随后的评估显示左侧胸腔积液,促使进一步调查。胸膜活检组织病理学分析和免疫组织化学证实PEAC, CK7和CDX2染色阳性。PET扫描显示左胸膜及肺部有恶性肿瘤,可能有淋巴结转移。患者接受了抗癌治疗,但疾病进展需要改变治疗方法。PEAC通常表现为非特异性呼吸道症状,最初常被误诊。诊断依赖于组织病理学检查和免疫组化染色,强调与原发性结直肠腺癌和常规肺腺癌鉴别的重要性。PEAC的治疗策略仍未得到充分探索,需要进一步研究以建立最佳的管理方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare case of adenocarcinoma with intestinal differentiation (PEAC) in the lung: Diagnostic challenges and treatment considerations
Adenocarcinoma with intestinal differentiation (PEAC) is a rare variant of lung adenocarcinoma, characterized by an enteric component and distinct immunohistochemical markers. This variant poses challenges in diagnosis and management due to its resemblance to primary colorectal adenocarcinoma and its unique clinical presentation. We present the case of a 76-year-old male with a one-month history of respiratory symptoms, initially managed as pneumonia. Subsequent evaluation revealed a left-sided pleural effusion, prompting further investigation. Histopathological analysis of pleural biopsy and immunohistochemistry confirmed PEAC, supported by positive staining for CK7 and CDX2. PET scan demonstrated malignancy in the left pleura and lung with likely metastasis to lymph nodes. The patient underwent anti-cancer treatment, but disease progression necessitated a change in therapy. PEAC often presents with nonspecific respiratory symptoms and is frequently misdiagnosed initially. Diagnosis relies on histopathological examination and immunohistochemical staining, emphasizing the importance of distinguishing it from primary colorectal adenocarcinoma and conventional lung adenocarcinoma. Treatment strategies for PEAC remain underexplored, and further research is warranted to establish optimal management approaches.
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