模仿肉芽肿性炎症的肺纺锤形细胞癌:罕见病例报告与文献简评

IF 5.1 Q1 ONCOLOGY
Lung Cancer: Targets and Therapy Pub Date : 2024-08-29 eCollection Date: 2024-01-01 DOI:10.2147/LCTT.S480969
Qian Liu, Jun Zhang, Mingqin Wei, Xue Zhou, Hao Sun, Youhong Dong, Dongdong Zhang
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引用次数: 0

摘要

背景:肺纺锤形细胞癌(PSCC)是一种高度恶性肿瘤,其组织病理学特征是细胞多形性。由于其发病率极低、影像学和临床表现不典型以及临床医生对其认识不足,PSCC 经常被误诊,导致治疗延误。在此,我们报告了一例罕见的PSCC病例,该病例最初被误诊为肉芽肿性炎症:一名 66 岁的男性因咳嗽和咯血等症状到当地医院就诊。胸部计算机断层扫描(CT)显示其右肺有肿块,未发现纵隔淋巴结病变。支气管镜检查未发现重大异常,细针穿刺活检结果显示为肉芽肿性炎症。尽管患者接受了抗感染治疗,但症状并没有明显改善。两个月后,随访的肺部 CT 扫描显示右肺上叶有一个明显增大的肿块,并伴有多处纵隔淋巴结病变。因此,他在我院接受了第二次 CT 引导下的肺活检。病理报告显示为 PSCC。由于经济拮据,没有进行基因检测。鉴于患者的整体身体状况较差,他无法接受全身化疗,只能接受姑息性放疗。针对右上肺叶肺癌和多个转移淋巴结的放疗剂量为 60 Gy,分 30 次进行。不幸的是,他未能按时复诊,6 个月后因病去世,电话随访时证实了这一点:结论:PSCC 是一种罕见但高度恶性的肺癌。结论:PSCC 是一种罕见但高度恶性的肺癌,必须进行多次病理活检才能准确、及时地诊断出这种疾病,这对早期治疗干预和改善患者预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary Spindle Cell Carcinoma Mimicking Granulomatous Inflammation: A Rare Case Report and Brief Review of the Literature.

Background: Pulmonary spindle cell carcinoma (PSCC), a highly malignant tumor, often exhibits cell pleomorphism, a histopathological characteristic. Owing to its extremely low incidence, atypical imaging and clinical presentations, and insufficient awareness among clinicians, PSCC is often misdiagnosed, which results in delays in treatment. Herein, we reported a rare case of PSCC that was initially misdiagnosed as granulomatous inflammation.

Case presentation: A 66-year-old male visited a local hospital with symptoms such as cough and hemoptysis. A computed tomography (CT) scan of the chest revealed a mass in his right lung, and no mediastinal lymphadenopathy was observed. Bronchoscopy showed no major abnormalities, and the results of fine needle aspiration biopsy showed granulomatous inflammation. Even though the patient received anti-infection treatment, his symptoms did not improve markedly. After two months, a follow-up CT scan of the lung showed a noticeably enlarged mass accompanied by multiple instances of mediastinal lymphadenopathy in the upper lobe of the right lung. Consequently, he underwent a second CT-guided lung biopsy at our hospital. The pathology report indicated PSCC. Due to financial constraints, genetic testing was not performed. Given his poor overall physical condition, the patient was unable to undergo systemic chemotherapy and instead received palliative radiotherapy. The prescribed radiotherapy dose for the right upper lobe lung cancer and multiple metastatic lymph nodes was 60 Gy, administered in 30 fractions. Unfortunately, he failed to adhere to scheduled follow-ups and succumbed to the disease 6 months later, as confirmed during a telephone follow-up.

Conclusion: PSCC is a rare but highly malignant lung cancer. Multiple pathological biopsies are necessary to accurately and promptly diagnose the disease, which is crucial for early treatment intervention as well as improving patient prognosis.

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来源期刊
CiteScore
8.10
自引率
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审稿时长
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