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一名急性髓系白血病患者的鼻窦髓系肉瘤

Myeloid Sarcoma of the Paranasal Sinuses in a Patient with Acute Myeloid Leukemia.

作者信息

Suzuki Jun, Harazaki Yoriko, Morita Shinkichi, Kaga Yoshiko, Nomura Kazuhiro, Sugawara Mitsuru, Katori Yukio

机构信息

Department of Otolaryngology-Head and Neck Surgery, Tohoku University School of Medicine.

Department of Otolaryngology, Tohoku Kosai Hospital.

出版信息

Tohoku J Exp Med. 2018 Oct;246(2):141-146. doi: 10.1620/tjem.246.141.

Abstract

Myeloid sarcoma (MS) is an uncommon extramedullary malignant tumor, and often represents a subgroup of acute myeloid leukemia (AML). MS of paranasal sinus origin is extremely rare. We report an uncommon case of sinonasal MS associated with AML, who was successfully treated with hematopoietic stem-cell transplantation. A 39-year-old male was admitted with complaints of left nasal obstruction and proptosis. Computed tomography and magnetic resonance imaging identified a left ethmoidal mass involving the maxillary sinus, the orbit, and the skull base. Nasal endoscopic examination detected a whitish homogeneous mass occupying the left nasal cavity. Although accumulation of atypical lymphocytes was suspected based on initial pathological inspection, immunohistochemical analysis showed myeloperoxidase-positive myeloid cells. Together with concomitant leukocytosis (149,000/µL) composed of myeloid blast cells and excess of myeloblasts in the bone marrow, the patient was diagnosed as sinonasal MS with AML with maturation (French-American-British Classification M2). The patient was treated by chemotherapy (remission induction therapy with daunorubicin and cytarabine; salvage chemotherapy with high-dose cytarabine), radiotherapy (30 Gy in 10 fractions) and allogeneic hematopoietic stem-cell transplantation, and followed up for 12 months with no recurrence. Early diagnosis is critical for the best improvement of MS. MS of the paranasal sinuses may easily be misdiagnosed as malignant lymphoma or poorly differentiated carcinoma. Prompt hematological and immunohistological investigations with suspicion of MS are essential for correct diagnosis. Furthermore, we concisely review nine previously reported patients with MS and indicate the importance of hematopoietic stem-cell transplantation for good prognosis.

摘要

髓系肉瘤(MS)是一种罕见的髓外恶性肿瘤,常为急性髓系白血病(AML)的一个亚组。起源于鼻窦的MS极为罕见。我们报告一例罕见的鼻窦MS合并AML病例,该患者通过造血干细胞移植成功治愈。一名39岁男性因左侧鼻塞和眼球突出入院。计算机断层扫描和磁共振成像显示左侧筛窦肿物累及上颌窦、眼眶和颅底。鼻内镜检查发现左侧鼻腔有一个白色均质肿物。尽管根据初始病理检查怀疑有非典型淋巴细胞聚集,但免疫组化分析显示髓过氧化物酶阳性的髓系细胞。结合骨髓中髓母细胞组成的白细胞增多(149,000/µL)以及髓母细胞过多,该患者被诊断为鼻窦MS合并成熟型AML(法美英分类M2)。患者接受了化疗(柔红霉素和阿糖胞苷诱导缓解治疗;大剂量阿糖胞苷挽救化疗)、放疗(10次分割共30 Gy)和异基因造血干细胞移植,并随访12个月无复发。早期诊断对MS的最佳改善至关重要。鼻窦MS易被误诊为恶性淋巴瘤或低分化癌。怀疑MS时及时进行血液学和免疫组织学检查对正确诊断至关重要。此外,我们简要回顾了9例先前报道的MS患者,并指出造血干细胞移植对良好预后的重要性。

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