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. 2018 Jan 24:6:2324709617752737.
doi: 10.1177/2324709617752737. eCollection 2018 Jan-Dec.

Oligosecretory Myeloma With Amyloidosis and Alopecia

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Oligosecretory Myeloma With Amyloidosis and Alopecia

Anum Bilal et al. J Investig Med High Impact Case Rep. .

Abstract

Amyloidosis is a systemic illness characterized by the extracellular deposition of abnormal proteins in body tissues and organs. In addition to renal involvement, amyloidosis can also present with a variety of skin manifestations, though rarely with alopecia. Sixteen cases of alopecia secondary to systemic amyloidosis are reported. There is one reported case that presented with alopecia universalis. We report a case of a 68-year-old woman presenting with alopecia universalis, rapid decline in kidney function, and nephrotic syndrome who was found to have multiple myeloma-associated AL amyloidosis (immunoglobulin light chain). Her serological workup including serum electrophoresis was negative and she underwent renal biopsy. Pathology revealed eosinophilic material within the mesangium that was Congo-red positive, had apple-green birefringence under polarized light, and ultramicroscopically appeared as fibrillary material. Subsequent bone marrow examination showed a diffuse increase in plasma cells with atypia indicating plasma cell neoplasm. This case underlines several interesting aspects of multiple myeloma and the way it may present with amyloidosis. The lack of monoclonal spike on electrophoresis yet positive light chain analysis deserves special attention by clinicians to avoid a missed diagnosis. The extensive skin involvement also raises several questions regarding the pathologic mechanisms of alopecia in a patient with amyloidosis.

Keywords: alopecia universalis; amyloidosis; multiple myeloma; nonsecretory multiple myeloma.

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Conflict of interest statement

Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Scalp picture showing alopecia.
Figure 2.
Figure 2.
Picture showing hair loss of arm, underarm.
Figure 3.
Figure 3.
Electron microscopy picture showing fibrils.

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References

    1. Breathnach SM. Amyloid and amyloidosis. J Am Acad Dermatol. 1988;18(1 pt 1):1-16. - PubMed
    1. Glenner GG. Amyloid deposits and amyloidosis. The beta-fibrilloses (first of two parts). N Engl J Med. 1980;302:1283-1292. - PubMed
    1. Khan MF, Falk RH. Amyloidosis. Postgrad Med J. 2001;77:686-693. - PMC - PubMed
    1. Falk RH, Comenzo RL, Skinner M. The systemic amyloidoses. N Engl J Med. 1997;337:898-909. - PubMed
    1. Sipe JD, Benson MD, Buxbaum JN, et al. Amyloid fibril protein nomenclature: 2010 recommendations from the nomenclature committee of the International Society of Amyloidosis. Amyloid. 2010;17:101-104. - PubMed

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