自动羽状边缘血涂片分析:在一例伴有多器官功能衰竭的弥散性血管内凝血病例中早期诊断出癌细胞增多症。

Marth Briers, Marnix Mylemans, Thomas Tousseyn, Lo Man Lai, Mercedeh Tajdar, Christine Van Laer
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摘要

癌细胞血症(Carcinocythemia)是指外周血中存在循环肿瘤细胞,当癌细胞微量存在时很难被发现。我们描述了一例 56 岁患者出现弥散性血管内凝血(DIC)和多器官衰竭的病例。尽管最初怀疑是败血症,但外周血涂片显示存在非典型细胞,主要位于羽毛边缘,因此推断诊断为原发性不明的癌细胞血症。我们的血液分析仪(Sysmex XN-9100)检测到高荧光细胞群,并用泛影角蛋白 AE1/AE3 进行免疫组化染色,证实了癌细胞的来源。患者在转诊至我院4天后死亡。尸检显示为多形性小叶乳腺癌(三阴性,雄激素受体阴性)。鉴于癌细胞病患者的临床表现十分敏锐,早期诊断对于指导治疗至关重要。本病例强调了优化当前工作流程的重要性,即依靠复杂的标记算法和增强型数字成像来帮助早期发现这种罕见病症。当患者出现不明原因的 DIC 并在血液分析仪上检测到高荧光信号时,应通过广泛的外周血显微镜检查积极排除癌细胞增多症。
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Automated feathered edge blood smear analysis: early diagnosis of carcinocythemia in a case of disseminated intravascular coagulation with multi-organ failure.

Carcinocythemia, known as the presence of circulating tumor cells in the peripheral blood, is difficult to detect when the carcinoma cells are minimally present. We describe a case of a 56-year-old patient presenting with disseminated intravascular coagulation (DIC) and multiple organ failure. Despite initial suspicion of sepsis, a peripheral blood smear showed the presence of atypical cells, mainly located at the feathered edge, leading to a presumptive diagnosis of carcinocythemia of unknown primary origin. The presence of a high-fluorescent cell population detected by our hematology analyzer (Sysmex XN-9100) and immunohistochemical staining with pancytokeratin AE1/AE3 confirmed the carcinoma cell origin. The patient died 4 days after referral to our hospital. Postmortem examination revealed a pleomorphic lobular breast carcinoma (triple-negative, androgen receptor-negative). Given the clinical acuity of patients with carcinocythemia, early diagnosis is essential to guide management. This case underscores the importance of optimizing current workflows relying on complex flagging algorithms and enhanced digital imaging to aid in the early detection of such rare condition. When patients present with DIC of unknown origin and high fluorescent signals are detected on the hematology analyzer, carcinocythemia should actively be ruled out by extensive microscopic peripheral blood examination.

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