» Articles » PMID: 12220287

D-penicillamine Treatment for Lipoid Proteinosis

Overview
Publisher Wiley
Specialties Dermatology
Pediatrics
Date 2002 Sep 11
PMID 12220287
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Lipoid proteinosis, a rare disorder inherited in an autosomal recessive fashion, is characterized by the deposition of hyaline-like material in the skin, mucous membranes, and other tissues. Perturbation of collagen metabolism has been suggested to play an important role in the pathogenesis. No effective therapy is available for the disease. The chelating agent D-penicillamine has long been used to treat several diseases. In addition to its immunosuppressive and anti-inflammatory effects, it also impairs fibroblast proliferation and inhibits the formation of the cross-links in collagen and elastin fibers. A 13-year-old girl was clinically and histologically diagnosed with lipoid proteinosis. We treated her with 600 mg/day of D-penicillamine for 2 years. The patient had improved clinically and histopathologically by the end of this treatment. We suggest D-penicillamine as a promising agent, even in low doses, for the treatment of lipoid proteinosis.

Citing Articles

Lipoid proteinosis; a rare pathology, requiring multidisciplinary input.

Fenech M, Yeo D BMJ Case Rep. 2023; 16(11).

PMID: 37931963 PMC: 10632804. DOI: 10.1136/bcr-2023-257108.


Intra-Familial Variability of Lipoid Proteinosis: An Indian Case Series.

Lohia K, Doshi B, Chougule N, Manjunathswamy Indian J Dermatol. 2022; 66(5):547-550.

PMID: 35068513 PMC: 8751709. DOI: 10.4103/ijd.IJD_475_19.


D-Penicillamine: The State of the Art in Humans and in Dogs from a Pharmacological and Regulatory Perspective.

Pugliese M, Biondi V, Gugliandolo E, Licata P, Peritore A, Crupi R Antibiotics (Basel). 2021; 10(6).

PMID: 34071639 PMC: 8229433. DOI: 10.3390/antibiotics10060648.


Lipoid Proteinosis presenting as beaded papules of the eyelid: report of three cases.

Wei Z, Labbe A, Liang Q BMC Ophthalmol. 2021; 21(1):35.

PMID: 33441084 PMC: 7805162. DOI: 10.1186/s12886-021-01802-z.


A novel nonsense mutation in exon 9 in the extracellular matrix protein 1 gene associated with lipoid proteinosis: A case report.

Ghazawi F, Proulx E, Jafarian F SAGE Open Med Case Rep. 2019; 7:2050313X19850359.

PMID: 31205714 PMC: 6537054. DOI: 10.1177/2050313X19850359.