“…9,10 The cytologic features of a metastatic focus would be expected, as was illustrated by Geisenger et al, 8 to show features of GCT, with at least a minority of the cells demonstrating nuclear atypia and mitotic activity. In the case reported by Liu et al, 3 FNA findings in aspirates of malignant GCT metastatic to a supraclavicular lymph node and liver revealed a high N:C ratio, vesicular nuclei with prominent nucleoli, pleomorphism and increased mitotic activity. These factors allowed the classification of the aspirate as malignant based solely on the cytologic features, independent of the metastatic nature of the tumor.…”
Section: Discussionmentioning
confidence: 86%
“…2 The diagnosis of malignant GCT is generally made when regional or distant metastases are present. 3 Histopathologically, primary malignant GCTs usually exhibit cytologic atypia, increased mitoses and necrosis. Metastatic GCTs most commonly occur in lymph nodes, lung, liver and bone, with most appearing several years after the initial diagnosis.…”
“…9,10 The cytologic features of a metastatic focus would be expected, as was illustrated by Geisenger et al, 8 to show features of GCT, with at least a minority of the cells demonstrating nuclear atypia and mitotic activity. In the case reported by Liu et al, 3 FNA findings in aspirates of malignant GCT metastatic to a supraclavicular lymph node and liver revealed a high N:C ratio, vesicular nuclei with prominent nucleoli, pleomorphism and increased mitotic activity. These factors allowed the classification of the aspirate as malignant based solely on the cytologic features, independent of the metastatic nature of the tumor.…”
Section: Discussionmentioning
confidence: 86%
“…2 The diagnosis of malignant GCT is generally made when regional or distant metastases are present. 3 Histopathologically, primary malignant GCTs usually exhibit cytologic atypia, increased mitoses and necrosis. Metastatic GCTs most commonly occur in lymph nodes, lung, liver and bone, with most appearing several years after the initial diagnosis.…”
“…11,12 This is the rarest of all sarcomas, with only a single case report available in the world literature describing its cytomorphology. 13 The patient was a 46-year-old woman with a midarm swelling with a synchronously enlarged axillary lymph node; 3-4 smears from the primary site were cellular, but lymph node aspirate showed only a few scattered cells. A cytologic diagnosis of malignancy was not possible 14 ; however, lymph node metastases are the only proof of malignancy in these cases and help in the diagnosis.…”
Granular cell tumors (GCTs) are uncommon soft tissue tumors, which are difficult to diagnose merely on clinical examination. Being an effective first-line investigation, the fine-needle aspiration cytology (FNAC) plays a significant role in its pre-operative recognition. However, as the tumor is likely to mimic certain other lesions, a cytopathologist needs to be aware of its characteristic cytomorphology. We report two cases of GCT who presented with subcutaneous swellings in the left lower back and the right-sided anterior abdominal wall for 6 and 2 months, respectively. Both the patients had a clinical diagnosis of lipoma/neurofibroma. FNAC was done in both. In the first case a cytodiagnosis of xanthogranuloma was suggested and GCT in the second. Subsequent histologic examination of both showed features of GCT. FNAC would aid in presumptive diagnosis of GCT.
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