ⓘ Congenital melanocytic nevus


ⓘ Bathing trunk nevus

The congenital melanocytic nevus is a type of melanocytic nevus found in infants at birth. This type of birthmark occurs in an estimated 1% of infants worldwide, it is located in the area of the head and neck 15% of the time.

  • Atypical nevus Becker s nevus Blue nevus Nevus spilus Spitz nevus Congenital melanocytic nevus Nevus of Ota Nevus anemicus Nevus depigmentosus Nevus anemicus
  • A melanocytic nevus also known as nevocytic nevus nevus - cell nevus and commonly as a mole is a type of melanocytic tumor that contains nevus cells
  • a cutaneous condition that may resemble a Spitz nevus or an acquired or congenital melanocytic nevus Melanoma List of cutaneous conditions Rapini, Ronald
  • Nevus spilus also known as speckled lentiginous nevus and zosteriform lentiginous nevus is a skin lesion that presents as a light brown or tan macule
  • Pseudomelanoma also known as a recurrent melanocytic nevus and recurrent nevus is a cutaneous condition in which melantic skin lesions clinically
  • Becker s nevus also known as Becker s melanosis Becker s pigmentary hamartoma nevoid melanosis and pigmented hairy epidermal nevus is a skin
  • described in patients with CMTC include nevus flammeus, hemangioma, nevus anemicus, cafe - au - lait spots, melanocytic nevus aplasia cutis and acral cyanosis
  • hemifacial microsomia craniofrontonasal syndrome, congenital melanocytic nevus melanoma, and certain congenital heart defects of the outflow tract. Recently
  • affected than men, and it is rare among Caucasian people. Nevus of Ota may not be congenital and may appear during puberty. A Q - switched 1064 nm laser
  • that vascular birthmarks are not hereditary. Congenital melanocytic nevus is a type of melanocytic nevus the medical term for what is colloquially called
  • Neurocutaneous melanosis is a congenital disorder characterized by the presence of congenital melanocytic nevi on the skin and melanocytic tumors in the leptomeninges
  • White sponge nevus WSN, is an autosomal dominant condition of the oral mucosa the mucous membrane lining of the mouth It is caused by a mutations in