Glomus tumours most commonly occurs in the subcutis of the distal extremities but rare renal glomus cell tumours have been reported.
Presentation is usually with a renal mass.
The histological appearances cover the spectrum from solid glomus tumour1 to glomangioma1,2 to glomangiomyoma1,3.
3/31 |
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pericellular staining in 3/31 |
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endothelial cells only in 3/31 |
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endothelial cells in 3/3 and myoid cells in 1/31 |
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Cells are surrounded by a continuous external lamina and contain numerous mitochondria, clusters of actin microfilaments and numerous pinocytotic vesicles.
Epithelioid glomus tumour: renal cell carcinoma: Immunohistochemistry distinguishes, with renal cell carcinoma positive for cytokeratins and EMA but negative for SMA.
Angiomyolipoma: should show all three components, smooth muscle, adipose tissue and thick walled vessels; it is positive for HMB-45 and Melan-A.
Lymphangioleiomyomatosis
Leiomyoma
Renal haemangioma
Juxtaglomerular cell tumour: affects young adults and is associated with severe hypertension, hyperkalaemia and high plasma renin levels.
This page last revised 30.4.2007.
©SMUHT/PW Bishop