Mao Mengke, Deng Shu
Department of Hematology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, Zhejiang 310006, P.R. China.
Oncol Lett. 2024 May 15;28(1):324. doi: 10.3892/ol.2024.14458. eCollection 2024 Jul.
Myeloid sarcoma (MS) is a rare extramedullary tumor mass that carries a high risk of progression to acute myeloid leukemia (AML), and patients with MS are commonly treated with the AML regimen. However, MS is frequently misdiagnosed due to its lack of clinical specificity. Patients with MS who harbor tumor protein p53 (TP53) mutations and complex karyotypes are considered to have a poorer prognosis. The present study reports a case of lymph node MS with TP53 (V173G)-related myelodysplastic syndrome (MDS). The mass was first considered to be a lymphoma and treated as such. However, following immunohistochemical analysis, which revealed cells positive for CD43, myeloperoxidase and CD117, the patient was later diagnosed with MS combined with MDS. The patient went into complete remission after the first cycle of chemotherapy, and showed a decrease in platelet, red blood cell and white blood cell counts following the second cycle of chemotherapy. After the third chemotherapy, agranulocytosis occurred, leading to refractory pneumonia and eventually death due to respiratory failure. MS with TP53-related MDS has a low incidence rate, a poor prognosis and a short survival time. The clinical manifestations of MS are non-specific and easy to misdiagnose, leading to delayed diagnosis and treatment, and ultimately worsening the prognosis of the patients. Therefore, a lymph node biopsy should be performed as soon as possible for patients with lymph node enlargement, and early treatment should be carried out to prolong the survival period.
髓系肉瘤(MS)是一种罕见的髓外肿瘤肿块,进展为急性髓系白血病(AML)的风险很高,MS患者通常采用AML方案治疗。然而,由于MS缺乏临床特异性,常被误诊。携带肿瘤蛋白p53(TP53)突变和复杂核型的MS患者被认为预后较差。本研究报告了1例伴有TP53(V173G)相关骨髓增生异常综合征(MDS)的淋巴结MS病例。该肿块最初被认为是淋巴瘤并按此治疗。然而,免疫组化分析显示细胞CD43、髓过氧化物酶和CD117呈阳性,该患者后来被诊断为MS合并MDS。患者在第一个化疗周期后完全缓解,第二个化疗周期后血小板、红细胞和白细胞计数下降。第三次化疗后发生粒细胞缺乏症,导致难治性肺炎,最终因呼吸衰竭死亡。伴有TP53相关MDS的MS发病率低、预后差、生存时间短。MS的临床表现无特异性,易误诊,导致诊断和治疗延误,最终使患者预后恶化。因此,对于淋巴结肿大的患者应尽快进行淋巴结活检,并尽早治疗以延长生存期。
Diagn Pathol. 2021-10-31
Int J Mol Sci. 2021-8-18
Pharmacol Ther. 2019-7-2
Indian J Hematol Blood Transfus. 2018-1