Dermoscopy of papular amyloidosis

Siham Boularbah, Sara Elloudi, Sabrina Oujdi, Meryem Soughi, Zakia Douhi, Hanane Baybay, Fatima Zahra Mernissi

Department of Dermatology, University Hospital Hassan II, Fes, Morocco

Corresponding author: Siham Boularbah, MD, E-mail: sihamboularbah1902@gmail.com

How to cite this article: Boularbah S, Elloudi S, Oujdi S, Soughi M, Douhi Z, Baybay H, Mernissi FZ. Dermoscopy of papular amyloidosis. Our Dermatol Online. 2025;16(2):195-196.
Submission: 02.09.2022; Acceptance: 11.05.2023
DOI: 10.7241/ourd.20252.18

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Papular amyloidosis (PA) is a form of primary cutaneous amyloidosis characterized by abnormal extracellular deposits of amyloid fibrils [1].

It presents as extremely pruriginous papular lesions, with the color of hyperkeratotic flesh, sitting electively on the anterior surfaces of the lower limbs. Diagnosis is based on histological examination. However, dermoscopy is of great help. Rare observations in the literature have focused on the interest of dermoscopy in the positive diagnosis of papular amyloidosis. The dermoscopic signs are pigmented granulations around a central crossroads histologically related to the amyloid deposit associated with striated pigmentation [2]. Herein, we describe a new case of dermoscopy of papular amyloidosis.

A 57-year-old female presented with pruritic, erythematous and violaceous lesions in the lower limbs evolving for seven years preceded by generalized pruritus and excoriated nodules persistent for fifteen years. A clinical examination revealed brownish, keratotic, and rough papules on confluent palpation in lichened plaques and purplish, erythematous nodules excoriated at the level of the extension faces of the two upper and lower limbs (Figs. 1a and 1b). Dermoscopy at the level of the papules revealed pigmented structures in “black peppercorns” arranged in rays around a central crossroads (Fig. 2). A skin biopsy confirmed the diagnosis of PA. The patient was put on dermocorticoids and the evolution was partially favorable with an improvement in the itching.

Figure 1: (a) Clinical picture showing a papulonodular rash on the lower limbs. (b) Dermoscopic image showing whitish central junction and grayish-brown granulations.
Figure 2: Dermoscopic image showing: Pigmented structures in the form of “black peppercorns” arranged in rays around a central crossroads.

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The examination of the patient was conducted according to the principles of the Declaration of Helsinki.

The authors certify that they have obtained all appropriate patient consent forms, in which the patients gave their consent for images and other clinical information to be included in the journal. The patients understand that their names and initials will not be published and due effort will be made to conceal their identity, but that anonymity cannot be guaranteed.

REFERENCES

1. Moon AO, Calamia KT, Walsh JS. Nodular amyloidosis:Review and long-term follow-up of 16 cases. Arch Dermatol. 2003;139:1157-9.

2. Gérard E, Ly S, Cogrel O, Pham-Ledard A, Fauconneau A, Penchet I, et al. Primary localized cutaneous nodular amyloidosis:A diagnostic and therapeutic challenge. Ann Dermatol Venereol. 2016;143:134-8.

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Conflict of Interest: The authors have no conflict of interest to declare.

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