颈淋巴结粒细胞性肉瘤:一个诊断挑战

Hemlata Das , Jagadish Hansa , Mahesh Chandra Sahu , Rabindra Nath Padhy
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引用次数: 1

摘要

粒细胞肉瘤是一种与急性或慢性髓性白血病相关的疾病,髓外部位由髓细胞母细胞和/或未成熟髓细胞组成。原发性粒细胞肉瘤成为一个诊断挑战,特别是在没有引用血液系统疾病或当淋巴结成为髓外与远程共发。这是一个15岁女孩的粒细胞肉瘤病例,表现为颈部右侧肿块,并伴有进行性吞咽困难和失语。组织形态学诊断通过免疫组织化学研究支持,该研究采用亲和素-生物素-过氧化物酶复合物技术对患者的福尔马林固定组织进行。由于孤立的宫颈肿块表现,恶性淋巴瘤的临床病理诊断仍然是一个难以捉摸的决定。此外,患者血流动力学稳定,外周血中无任何白血病母细胞存在。结论对颈部肿块组织进行免疫组化检查有助于正确诊断。骨髓穿刺活检进一步证实了诊断。髓系标志物的最后试验是圆细胞瘤鉴别诊断的最后选择。肿瘤细胞对CD68、CD34、CD117和髓过氧化物酶有免疫反应,提示髓系肉瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
“Granulocytic sarcoma of cervical lymphnode: A diagnostic challenge”

Introduction

Granulocytic sarcoma is an event associated with acute or chronic myeloid leukemia in which, the extramedullary site consists of myeloid blasts and/or immature myeloid cells. Primary granulocytic sarcoma becomes a diagnostic challenge especially in the absence of cited hematological disorder or when lymphnode becomes an extramedullary with remote co-incidence.

Presentation of case

This is a case of granulocytic sarcoma in a 15-year-old girl, who presented with a mass in the right side of neck, along with progressive dysphagia and aphasia. Histomorphologic diagnosis of the tissue was supported by immunohistochemical study with Avidin-biotin-peroxidase complex technique that was performed on formalin fixed tissue from the patient.

Discussion

The clinicopathologic diagnosis remains an elusive decision with a malignant lymphoma, because of the isolated cervical mass presentation. Moreover, the patient was hemodynamically stable without the presence of any leukemic blast cell in the peripheral blood.

Conclusion

Immunohistochemical study of the tissue from the neck mass helped to reach a correct diagnosis. The diagnosis was further reconfirmed on bone marrow trephine biopsy. A final trial with myeloid panel markers was the last alternatives to all differential diagnosis to round cell tumor. Tumor cells were immunoreactive to CD68, CD34, CD117 and myeloperoxidase, suggesting myeloid sarcoma.

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