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Home > Resident Case Studies > Week 12 Case 1 > Case 1 Discussion

RESIDENT CASE STUDIES

Week 12 July 7 - July 11, 2003: Case 1  

Table of Contents | List of Diagnoses | Case 1 | Case 2

61 year old female with abdominal wall mass

Discussion
Granular cell tumor (GCT) is a benign neural tumor characterized by large granular-appearing eosinophilic cells.1 Granular cell tumors are tumors that may arise from various soft tissue, including extremity and visceral sites.2 These lesions often are multifocal (10-15% of cases), but usually benign.1,2 GCT can occur at any age, but commonly in the adults. It is very rare in children.1 It appears to be more common in women. 

GCT tends to be poorly circumscribed. The cells are rounded, polygonal or slightly spindled. The nuclei may be small and dark, or large with vesicular chromatin.1 The cytoplasm is eosinophilic with fine to coarse granules which represent phagolysosomes, strongly PAS-positive, diastatse resistance.1 There may be nuclear atypia occasionally, but this does not necessarily indicate malignancy.1

Granular cells do not contain glycogen. Immunohistochemically GCT is positive for S100, NSE, CD68.

Rarely, there may be malignant granular cell tumor. Features such as necrosis, spindling, vesicular nuclei with prominent nucleoli, greater than 2 mitoses/10 HP, high N/C ratio and pleomorphism are suggestive of malignancy. Tumors with 3 or more of these features are considered malignant and have, approximately, a 40% risk of causing death.1 

References:

1Weiss SW, Goldblum JR. Enzinger and Weiss’s soft tissue tumor. 4th Eds. Mosby.

2Elkousy H, Harrelson J, Dodd L, et al. Granular cell tumors of the extremities. Clin Orthop. 2000 Nov;(380):191-8.