Atypical lichen myxedematosus

Classification	D ICD-10: L98.5;
External resources	Orphanet: 86797;

Atypical lichen myxedematosus
Other names	Intermediate lichen myxedematosus[1]
Specialty	Dermatology

Atypical lichen myxedematosus is a skin condition caused by fibroblasts producing abnormally large amounts of mucopolysaccharides.[2]^:186

References

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Atypical lichen myxedematosus". www.orpha.net. Retrieved 18 April 2019.
James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.

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Mucinosis/Lichen myxedematosus (L98.5, 701.8)
Localized lichen myxedematosus	Discrete papular lichen myxedematosus Acral persistent papular mucinosis Self-healing papular mucinosis/Self-healing juvenile cutaneous mucinosis Papular mucinosis of infancy Atypical lichen myxedematosus Atypical tuberous myxedema Nodular lichen myxedematosus
Other primary mucinoses	Cutaneous focal mucinosis Cutaneous lupus mucinosis Eccrine mucinosis Alopecia mucinosa Perifollicular mucinosis Stiff skin syndrome Generalized lichen myxedematosus
Secondary mucinoses	Basal-cell carcinoma Granuloma annulare

Classification	D ICD-10: L98.5
External resources	Orphanet: 86797