Acral persistent papular mucinosis

Acral persistent papular mucinosis
Acral persistent papular mucinosis
Specialty	Dermatology

Acral persistent papular mucinosis is a skin condition caused by fibroblasts producing abnormally large amounts of mucopolysaccharides, characterized by bilaterally symmetrical, flesh-colored papules localized to the hands and wrists.[1]^: 185[2]

References

James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.

External links

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[Andrews-1] James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.

[Bolognia-2] Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.

Classification	D ICD-10: L98.5
External resources	Orphanet: 90396

Mucinosis/Lichen myxedematosus
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

Acral persistent papular mucinosis

See also

References

External links