Cantone Elena, Cavaliere Michele, Di Lullo Antonella Miriam, Guadagno Elia, Iengo Maurizio
Department of Neuroscience, Ear, Nose and Throat Section, Pathology Section, 'Federico II' University of Naples, I-Naples 80100, Italy.
Department of Advanced Biomedical Sciences, Pathology Section, 'Federico II' University of Naples, I-Naples 80100, Italy.
Oncol Lett. 2016 Oct;12(4):2777-2781. doi: 10.3892/ol.2016.5009. Epub 2016 Aug 16.
Granulocytic sarcoma (GS) is a rare extramedullary manifestation of acute myeloid leukemia (AML). GS may develop simultaneously to AML or as a relapse of leukemia, particularly following allogeneic hematopoietic stem cell transplant. Subperiosteal bone, lymph nodes and skin are commonly involved, whereas rhinopharyngeal involvement is less common, with only 14 cases reported in the literature. Due to its rarity, rhinopharyngeal GS may lead to diagnostic pitfalls, particularly when it is poorly differentiated or is without concomitant marrow involvement. Thus, immunohistochemical findings play a key role in diagnosis. The current report describes a case of a 53-year-old female suffering from rhinopharyngeal GS and with a history of AML treated with chemotherapy and radiotherapy, focusing on the importance of the immunohistochemical pattern to assess the right diagnosis. Recent studies have demonstrated that the immunophenotype is of utmost importance for the diagnosis of GS. The high expression of myeloperoxidase (MPO) is common in GS; however, ~30% of GSs do not contain MPO. Therefore, the presence of other markers is required to confirm the diagnosis of GS.
粒细胞肉瘤(GS)是急性髓系白血病(AML)一种罕见的髓外表现形式。GS可能与AML同时发生,或作为白血病复发出现,尤其是在异基因造血干细胞移植后。骨膜下骨、淋巴结和皮肤是常见受累部位,而鼻咽部受累较少见,文献中仅报道了14例。由于其罕见性,鼻咽部GS可能导致诊断陷阱,特别是当它分化不良或无骨髓受累时。因此,免疫组化结果在诊断中起关键作用。本报告描述了一例53岁女性患有鼻咽部GS且有AML病史,曾接受化疗和放疗,重点阐述免疫组化模式对正确诊断的重要性。最近的研究表明,免疫表型对GS的诊断至关重要。髓过氧化物酶(MPO)的高表达在GS中很常见;然而,约30%的GS不含MPO。因此,需要其他标志物的存在来确诊GS。