Table 2. Review of congenital tufted angiomas described in the literature.
|
Patient’s sex |
Clinical manifestations |
Site |
Course to regression |
Complications |
Lam et al6 |
2 cases ♀ ♂ |
6x3cm blue plaque 12x7 cm erythematous macula |
Thorax Right scapula |
3 years 5 years |
None |
Jang et al7 |
1 case ♀ |
5x0.5 cm purple-erythematous plaque |
Abdomen |
10 months |
None |
Enjolras et al8 |
1 case ♂ |
Purple-erythematous mass |
Right leg |
< 1year |
Kasabach-Merritt syndrome |
Igarashi et al9 |
9 cases |
Unknown |
9 cases |
Unknown course |
Unknown |
Kim et al10 |
1 case ♀ |
6x6 cm subcutaneous mass with blue-erythematous telangiectasias |
Right thigh |
Course unknown |
Unknown |
Kimura et al11 |
3 cases 2 ♂ 1 ♀ |
Unknown |
2Leg Hand |
17 month 6 years Unknown |
Unknown |
Kato et al12 |
1 case ♂ |
Unknown |
Ankle |
6 months |
Unknown |
Wong et al13 |
5 cases (1 congenital) ♀ |
Plaque |
Right leg |
PR in 1 year |
None |
Satter et al14 |
1 case ♀ |
4x2cm brown erythematous plaque |
Right arm |
Persisted after 7 years |
None |
Browning et al15 |
5 cases 3 ♂ and 2 ♀ |
|
3 head 1 left arm 1 right leg |
4 CR in 4-15 months 1 PR in 1 year |
None |
Barco et al16 |
1 case ♂ |
5 cm purple plaque |
Right arm |
PR in 1 year |
None |
Our case |
♀ |
4x2 cm purple plaque |
Medial aspect of right arm |
PR in 6 months |
None |
CR: complete regression. PR: partial regression.