Glomeruloid hemangioma is a distinctive vascular tumor first described in 1990 when found to be associated with POEMS syndrome and Castleman disease.
[1][2] Glomeruloid hemangiomas can manifest as wine-red sessile or pedunculated papules, papulonodules, subcutaneous bluish compressible tumors, or small, firm, reddish-violaceous, dome-shaped papules.
[3] They mostly reside on the trunk and proximal limbs and range in size from a few millimeters to a few centimeters in diameter.
[10] Rarely glomeruloid hemangiomas can occur in individuals with no systematic conditions.
[11] The histopathologic examination displays well-defined, dispersed dermal structures in different sizes that have resemblance to renal glomeruli.