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Journal of Clinical & Experimental Pathology - Localized Cutaneous Amyloidosis Revealed by Immunohistochemistry: An Interesting Diagnostic Tool
ISSN: 2161-0681

Journal of Clinical & Experimental Pathology
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  • Image Article   
  • J Clin Exp Pathol
  • DOI: 10.4172/2161-0681.1000002

Localized Cutaneous Amyloidosis Revealed by Immunohistochemistry: An Interesting Diagnostic Tool

Derqaoui Sabrine1*, Essaoudi Mohamed Amine2 and Elktaibi Abderrahim2
1Department of Pathology, Mohamed V Military Instruction Hospital, Rabat, Morocco
2Department of Medicine and Pharmacy of Rabat, Mohamed V University, Rabat, Morocco
*Corresponding Author: Derqaoui Sabrine, Department of Pathology, Mohamed V Military Instruction Hospital, Rabat, Morocco, Email: s.derqaoui@gmail.com

Received: 09-Mar-2022 / Manuscript No. JCEP-22-56584 / Editor assigned: 11-Mar-2022 / PreQC No. JCEP-22-56584 (PQ) / Reviewed: 01-Apr-2022 / QC No. JCEP-22-56584 / Revised: 08-Apr-2022 / Manuscript No. JCEP-22-56584 (R) / Published Date: 15-Apr-2022 DOI: 10.4172/2161-0681.1000002

Keywords: cytokeratin, Localised Cutaneous Amyloidosis

Case Description

An 85-year-old woman had a lightly pruritic firm plaque on the forearm for 28 years. She had no major medical trouble and she didn’t receive any medical treatment before visiting dermatology’s department. Biopsy specimen from the lesion revealed an amorphous acellular eosinophilic deposit (black star) in the papillary dermis (Figures 1A and 1B). The overlying epidermis was of normal thickness without hyperkeratosis. The deposits were negative for Congo red staining (Figure 1C), without typical green birefrengence on polarizing microscopy (Figure 1D). On immunohistochemistry, they stained diffusely positive with pan cytokeratin AE1/AE3 (Figure 2).

2161-0681-dermal

Figure 1: Amyloid dermal deposits : HE staining at (A) low power and (B) high power, These deposits are negative for (C) Congo red), without typical green birefringence on (D) polarizing microscopy.

2161-0681-positive

Figure 2: Immunohistochemistry, positive staining for pan cytokeratin AE1/AE3.

Localised Cutaneous Amyloidosis (LCA) is defined by the deposition of amyloid in the skin with the absence of systemic involvement [1]. LCA can be divided into: primary and secondary LCA [1]. The latter, is observed in several inflammatory and neoplastic skin disordes such as seborrheic keratosis, Bowen’s disease and basal cell carcinoma [1,2]. Primary cutaneous amyloid is a chronic pruritic condition [1]. On histology, PCA shows amorphous eosinophilic deposits in the papillary dermis. Definite diagnosis requires special stains and sometimes immnohistochemistry [3] Amyloid is usually positive with Congo red staining; and shows green birefringence in polarizing microscopy. However, Cong red staining might be negative; as in the present case. Immunohistochemistry for cytokeratins (high molecular weight cytokeratins and ck 5/6) represents a useful diagnostic tool in LCA, because Congo red staining may not detect small deposits. In the study of et al., the authors recommend performing IHC for high molecular weight cytokeratins to exclude the diagnosis, when Congo red is negative [4]. These findings confirm the origin of amyloid: epidermal keratins due to epidermal long term damage [3].

References

Citation: Sabrine D, Amine EM, Abderrahim E (2022) Localized Cutaneous Amyloidosis Revealed by Immunohistochemistry : An Interesting Diagnostic Tool. J Clin Exp Pathol S1:002. DOI: 10.4172/2161-0681.1000002

Copyright: © 2022 Sabrine D, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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