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Case Reports
. 2022 Aug 13:15:1639-1642.
doi: 10.2147/CCID.S378253. eCollection 2022.

Primary Localized Cutaneous Nodular Amyloidosis Presenting as Milia: An Unusual Clinical Manifestation

Affiliations
Case Reports

Primary Localized Cutaneous Nodular Amyloidosis Presenting as Milia: An Unusual Clinical Manifestation

Yanqing Wang et al. Clin Cosmet Investig Dermatol. .

Abstract

Primary localized cutaneous nodular amyloidosis (PLCNA) is rare and clinically noncharacteristic, presenting mostly as plaque-like lesions. We report a case of a progressively larger erythematous plaque following a contusion of the skin on the right zygomatic area, which was strangely covered with recurrent scattered 2 mm whiteish blisters to the extent that it was misdiagnosed as a herpesvirus infection several times over a decade. Pathology and special staining diagnosed nodular amyloidosis with milia.

Keywords: local trauma; milia; plaque; primary localized cutaneous nodular amyloidosis.

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Conflict of interest statement

The authors report no conflicts of interest related to this work.

Figures

Figure 1
Figure 1
Orange‒yellow plaque with overlying scattered 2 mm whiteish blisters on the right zygomatic area.
Figure 2
Figure 2
Three pathological images of nodular amyloidosis. (A) Deposition of acellular amorphous eosinophilic materials over the entire dermis and subcutis (H&E, ×200). (B) The amyloid deposits were positive for Congo red staining, and keratinous cysts were found in the superficial dermis. The arrows indicate the sites of amyloid deposits.(Congo red staining, ×200) (C) The amyloid deposits were positive for crystal violet staining, and keratinous cysts were found in the superficial dermis. The arrows indicate the sites of amyloid deposits. (Crystal violet staining, ×200).

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References

    1. Mena L, Carrasco C, Folch H, de la Parra R, Carreño L. Primary cutaneous nodular amyloidosis associated with the injection of autologous fat. Clin Exp Dermatol. 2021;46:552–554. doi:10.1111/ced.14429 - DOI - PubMed
    1. Vestery JP, Tidman MJ, Mclaren KM. Primary nodular cutaneous amyloidosis – long-term follow-up and treatment. Clin Exp Dermatol. 1994;19:159–162. doi:10.1111/j.1365-2230.1994.tb01148.x - DOI - PubMed
    1. Ung CY, Carr NJ, Ardern-Jones MR. Primary cutaneous nodular amyloidosis associated with psoriasis. Clin Exp Dermatol. 2014;39:608–611. doi:10.1111/ced.12347 - DOI - PubMed
    1. Dickison P, Howard V, Wylie B, Smith SD. Localized axillary milia en plaque: a rare cutaneous case presentation of systemic amyloidosis. Clin Exp Dermatol. 2016;41(7):764–767. doi:10.1111/ced.12914 - DOI - PubMed
    1. Yahya H. Idiopathic multiple eruptive milia: report of a case in a Nigerian woman. Niger J Clin Pract. 2018;21:395–396. doi:10.4103/njcp.njcp_43_17 - DOI - PubMed

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