Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma) Follow-up
- Author: Tina S Chen, MD; Chief Editor: Dirk M Elston, MD more...
Further Inpatient Care
Neonatal epidermolytic hyperkeratosis (EHK, bullous congenital ichthyosiform erythroderma [bullous CIE]) patients may need to be transferred to the neonatal ICU for monitoring of infection, sepsis, electrolyte imbalance, and administration of intravenous fluids or antibiotics.
Further Outpatient Care
Schedule routine follow-up visits as needed for symptomatic relief or to follow laboratory studies during systemic therapies for epidermolytic hyperkeratosis (EHK, bullous congenital ichthyosiform erythroderma [bullous CIE]).
Inpatient & Outpatient Medications
Inpatient medications for epidermolytic hyperkeratosis (EHK, bullous congenital ichthyosiform erythroderma [bullous CIE]) are determined by clinical need to treat secondary effects of this condition (eg, sepsis, electrolyte imbalance). Outpatient medications for epidermolytic hyperkeratosis are determined by what works best with each individual patient (see Medication).
Transfer
Transfer of infants with epidermolytic hyperkeratosis (EHK, bullous congenital ichthyosiform erythroderma [bullous CIE]) to the neonatal ICU to monitor for sepsis and electrolyte imbalance may be necessary.
Complications
Patients with epidermolytic hyperkeratosis (EHK, bullous congenital ichthyosiform erythroderma [bullous CIE]) are at an increased risk for recurrent infections, and a pungent smell can be noted.
Prognosis
Epidermolytic hyperkeratosis (EHK, bullous congenital ichthyosiform erythroderma [bullous CIE]) is a lifelong condition. Some patients may experience amelioration of symptoms as they age.
Patient Education
Educate patients with epidermolytic hyperkeratosis (EHK, bullous congenital ichthyosiform erythroderma [bullous CIE]) about the potential of passing the chromosomal defect on to offspring.
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