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.