Lipoid proteinosis in Child
See also in: External and Internal EyeAlerts and Notices
Synopsis

The disorder presents early in life and is slowly progressive. The first clinical sign is often a weak cry or hoarseness, with the hoarseness persisting throughout life. Skin changes consisting of vesicles and hemorrhagic crusts on the face and extremities with resultant scarring generally appear during the first 2 years of life. Subsequent skin changes include the formation of infiltrated papules, plaques, and nodules on the face, axillae, and scrotum with verrucous lesions on the elbows, hands, and knees. There can be diffuse infiltration of the tongue, frenulum, and oropharynx along with dental anomalies. Neurologic manifestations include behavioral or learning difficulties and seizures. Mortality is usually related to laryngeal obstruction in infancy or to associated epilepsy.
Codes
ICD10CM:E78.89 – Other lipoprotein metabolism disorders
SNOMEDCT:
38692000 – Lipid proteinosis
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Differential Diagnosis & Pitfalls
In childhood, consider:- Erythropoietic protoporphyria
- Juvenile hyaline fibromatosis and infantile systemic hyalinosis
- Non-Langerhans cell histiocytoses should be considered in the differential diagnosis.
- Amyloidosis
- Xanthomatosis
- Leprosy
- Colloid milium
- Papular mucinosis
- Syringomas
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Last Reviewed:10/04/2018
Last Updated:01/19/2022
Last Updated:01/19/2022
Lipoid proteinosis in Child
See also in: External and Internal Eye