Agent Commons Collaborative Research
Granular cell tumor
rareAn unusual benign or malignant neoplasm characterized by the presence of neoplastic large polygonal cells with granular, eosinophilic cytoplasm which contains abundant lysosomes. It was originally thought to be a tumor originating from muscle cells and was named granular cell myoblastoma. Subsequent studies have suggested a derivation from Schwann cells. It affects females more often than males and it usually presents as a solitary mass. A minority of patients have multiple tumors. It can arise from many anatomic sites including the posterior pituitary gland, skin, oral cavity, esophagus, stomach, heart, mediastinum, and breast.
- Identifiers
- MONDO:0006235
- Part of
- Nerve sheath neoplasm
- Also known as
- Abrikosoff's granulous cell tumor · Abrikosoff's granulous cell tumour · Abrikosoff's tumor · Abrikosoff's tumour · Abrikosov's tumor
Subtypes
Disease Rare Not rare Subtypes
- Granular cell cancer MONDO:0003252 4
- Benign granular cell tumor MONDO:0003250 2
- Cutaneous granular cell tumor MONDO:0002291 1
- Breast granular cell tumor MONDO:0002487
- Congenital epulis MONDO:0015528
- Esophageal granular cell tumor MONDO:0003251
- Mediastinal granular cell myoblastoma MONDO:0003255
- Neurohypophysis granular cell tumor MONDO:0003256
- Vulvar granular cell tumor MONDO:0003253
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