What is the cause of a facial rash in a 20-day-old neonate?

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Differential Diagnosis for Rash on the Face of a 20-Day-Old Infant

Single Most Likely Diagnosis

  • Erythema Toxicum Neonatorum: This is a common, benign condition that appears as a rash on the face and body of newborns, typically within the first few days of life but can persist. It is characterized by small, yellow or white bumps on a red base and is thought to be an allergic reaction to the shift in environment from the womb to the outside world.

Other Likely Diagnoses

  • Acne Neonatorum: Also known as neonatal acne, this condition is caused by exposure to maternal hormones and can appear as small pimples or comedones on the face, particularly the nose, chin, and forehead.
  • Seborrhoeic Dermatitis (Cradle Cap): This condition can cause a rash on the face, scalp, and other areas, characterized by a greasy, yellow, scaly appearance. It's relatively common in infants and is thought to be related to overactive sebaceous glands.
  • Atopic Dermatitis (Eczema): Although less common at this age, atopic dermatitis can present as a rash on the face, especially on the cheeks, and is associated with itching and dry skin.

Do Not Miss Diagnoses

  • Congenital Infections (e.g., Congenital Syphilis, Rubella, CMV): These infections can cause a variety of skin manifestations, including rashes, and are critical to diagnose early due to their potential for serious complications.
  • Herpes Simplex Virus (HSV) Infection: Neonatal HSV can present with skin, eye, or mouth lesions and is a medical emergency requiring prompt antiviral treatment.
  • Staphylococcal Scalded Skin Syndrome (SSSS): Caused by staphylococcal toxins, SSSS can lead to widespread skin blistering and peeling, starting on the face, and is life-threatening if not treated promptly.

Rare Diagnoses

  • Incontinentia Pigmenti: A genetic disorder that can cause skin lesions, including a rash, typically following the lines of Blaschko, and is often associated with other systemic manifestations.
  • Epidermolysis Bullosa: A group of genetic conditions that result in blistering of the skin and mucous membranes, which can appear as a rash or blisters on the face and other areas.
  • Langerhans Cell Histiocytosis: A rare disorder characterized by an overproduction of Langerhans cells, which can lead to skin lesions, among other systemic symptoms.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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