Thakur Brijesh, Varma Kachnar, Misra Vatsala, Chauhan Smita
Assistant Professor, Department of Pathology, SGRRIM & HS , Dehradun, India .
J Clin Diagn Res. 2013 Aug;7(8):1704-6. doi: 10.7860/JCDR/2013/5582.3260. Epub 2013 Aug 1.
Granulocytic sarcoma is a rare variant of a myeloid malignancy, which shows an extra-medullary tumour mass which is composed of myeloblasts and myeloid precursors with varying degrees of differentiation. It occurs most commonly in bone, periosteum, soft tissue, lymph nodes, and skin; although it can occur anywhere throughout the body. Here, we are reporting two cases of orbital granulocytic sarcoma in children, which presented clinically with proptosis and periorbital swellings, which were first diagnosed by Fine Needle Aspiration Cytology (FNAC). Later, peripheral blood and bone marrow aspirate examinations revealed the evidence of Acute Myeloid Leukaemia (AML). These cases are being documented to demonstrate the utility and diagnostic accuracy of FNAC in evaluation of this entity, in cases of unsuspected AML. Recognition of this rare entity is important, because giving an early aggressive chemotherapy can cause regression of the tumour and thus improve the patient survival.
粒细胞肉瘤是一种罕见的髓系恶性肿瘤变体,表现为髓外肿瘤肿块,由不同分化程度的成髓细胞和髓系前体细胞组成。它最常见于骨骼、骨膜、软组织、淋巴结和皮肤;尽管它可发生于全身任何部位。在此,我们报告两例儿童眼眶粒细胞肉瘤病例,临床上表现为眼球突出和眶周肿胀,最初通过细针穿刺抽吸细胞学检查(FNAC)诊断。后来,外周血和骨髓穿刺检查发现了急性髓系白血病(AML)的证据。记录这些病例是为了证明FNAC在评估未怀疑AML的此类病例中的实用性和诊断准确性。认识到这种罕见实体很重要,因为早期积极化疗可使肿瘤消退,从而提高患者生存率。