Marked Leukocytosis and Subclavian Vein Occlusion from Pancoast Tumor Mimicking Cellulitis: A Case Report.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI:10.1159/000551217
Hiroshi Shintani, Naoki Kataoka
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引用次数: 0

Abstract

Introduction: Lung cancer can present with atypical clinical manifestations that may mimic benign conditions. We report an extremely rare case of lung cancer initially misdiagnosed as cellulitis due to unilateral upper limb swelling and elevated inflammatory markers.

Case presentation: A 65-year-old woman with a history of heavy smoking presented with progressive swelling and pain in the left upper limb, accompanied by leukocytosis and elevated inflammatory markers. She was initially diagnosed with cellulitis and treated with antibiotics without improvement. Contrast-enhanced computed tomography revealed a left apical lung tumor invading the chest wall and occluding the subclavian vein. Histopathological examination confirmed primary non-small-cell lung carcinoma, favoring adenocarcinoma. The patient also exhibited tumor-associated extreme leukocytosis and experienced rapid disease progression despite supportive care, dying 37 days after admission.

Discussion: This case illustrates the diagnostic challenges posed by lung cancer presenting with atypical, infection-like manifestations. Pancoast tumors involving the subclavian vein can cause upper limb edema, while tumor-associated leukocytosis can mimic inflammatory responses. Because extreme leukocytosis in solid tumors is associated with poor prognosis, early recognition is crucial.

Conclusion: Even when clinical findings suggest infection, malignancy should be considered in the differential diagnosis, particularly in patients with risk factors such as smoking or advanced age. Prompt chest imaging is essential to avoid diagnostic delay in such cases.

模拟蜂窝织炎的Pancoast肿瘤伴明显白细胞增多和锁骨下静脉阻塞1例。
简介:肺癌可以呈现非典型的临床表现,可能模仿良性条件。我们报告一例极为罕见的肺癌病例,由于单侧上肢肿胀和炎症标志物升高,最初被误诊为蜂窝织炎。病例介绍:65岁女性,有重度吸烟史,左上肢进行性肿胀和疼痛,伴有白细胞增多和炎症标志物升高。她最初被诊断为蜂窝织炎,并接受抗生素治疗,但没有好转。增强计算机断层扫描显示一左肺顶端肿瘤侵入胸壁并阻塞锁骨下静脉。组织病理学检查证实为原发性非小细胞肺癌,倾向于腺癌。患者还表现出肿瘤相关的极端白细胞增多,尽管有支持治疗,但病情进展迅速,在入院后37天死亡。讨论:本病例说明了以非典型感染样表现的肺癌所带来的诊断挑战。累及锁骨下静脉的Pancoast肿瘤可引起上肢水肿,而肿瘤相关的白细胞增多可模拟炎症反应。由于实体瘤中白细胞过多与预后不良有关,因此早期识别至关重要。结论:即使临床表现提示感染,在鉴别诊断时也应考虑恶性肿瘤,特别是有吸烟或高龄等危险因素的患者。在这种情况下,及时的胸部成像是必不可少的,以避免诊断延误。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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