Congenital dermal melanocytosis in Infant/Neonate
See also in: AnogenitalAlerts and Notices
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Synopsis
 
                     
               Congenital dermal melanocytosis (CDM), previously referred to as Mongolian spot, is one of the most commonly encountered newborn pigmented lesions. It is a benign, ill-defined, blue-to-gray patch present at birth or shortly after. CDM patches are commonly seen in the sacrococcygeal area in infants of Asian or African descent but may be found on any cutaneous surface in infants of all ethnicities. The pigmentation becomes most intense at 1 year of age, reaches its peak diameter by 2 years of age, and usually fades completely by adulthood.
CDM occurs due to the delayed disappearance of dermal melanocytes within the deep dermis.
Related topic: acquired dermal melanocytosis
            CDM occurs due to the delayed disappearance of dermal melanocytes within the deep dermis.
Related topic: acquired dermal melanocytosis
Codes
                  ICD10CM:
Q82.8 – Other specified congenital malformations of skin
SNOMEDCT:
40467008 – Mongolian spot
            Q82.8 – Other specified congenital malformations of skin
SNOMEDCT:
40467008 – Mongolian spot
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               Last Reviewed:08/27/2024
Last Updated:08/28/2024
            
               
             Last Updated:08/28/2024
 Patient Information for Congenital dermal melanocytosis  in Infant/Neonate
Patient Information for Congenital dermal melanocytosis  in Infant/Neonate
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        Congenital dermal melanocytosis  in Infant/Neonate
                  See also in: Anogenital