Vol 6, No 4 (2020)
Case report
Published online: 2020-12-02
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Primary cutaneous amyloidosis — case report

Kamila Jaworecka1, Robert Kijowski1, Elżbieta Ostańska2, Piotr Mazur-Chromiak1, Adam Reich13
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Forum Dermatologicum 2020;6(4):126-129.
Affiliations
  1. Klinika Dermatologii, Kliniczny Szpital Wojewódzki nr 1 im. F. Chopina w Rzeszowie
  2. Kliniczny Zakład Patomorfologii, Kliniczny Szpital Wojewódzki Nr 1 w Rzeszowie
  3. Zakład Dermatologii, Instytut Nauk Medycznych, Kolegium Nauk Medycznych, Uniwersytet Rzeszowski

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Vol 6, No 4 (2020)
CASE STUDY
Published online: 2020-12-02

Abstract

Amyloidosis refers to a group of diseases in which tissues and organs accumulate amyloid — a protein with an abnormal structure, which leads to impairment of their function. There are systemic forms of amyloidosis, involving the internal organs and skin, and cutaneous ones, where the disease process affects only the skin. Here, we present a case of a seventy-year-old woman diagnosed with primary cutaneous amyloidosis.

Abstract

Amyloidosis refers to a group of diseases in which tissues and organs accumulate amyloid — a protein with an abnormal structure, which leads to impairment of their function. There are systemic forms of amyloidosis, involving the internal organs and skin, and cutaneous ones, where the disease process affects only the skin. Here, we present a case of a seventy-year-old woman diagnosed with primary cutaneous amyloidosis.

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Keywords

amyloid; gammopathy; amyloidosis

About this article
Title

Primary cutaneous amyloidosis — case report

Journal

Forum Dermatologicum

Issue

Vol 6, No 4 (2020)

Article type

Case report

Pages

126-129

Published online

2020-12-02

Page views

974

Article views/downloads

46

DOI

10.5603/FD.a2020.0018

Bibliographic record

Forum Dermatologicum 2020;6(4):126-129.

Keywords

amyloid
gammopathy
amyloidosis

Authors

Kamila Jaworecka
Robert Kijowski
Elżbieta Ostańska
Piotr Mazur-Chromiak
Adam Reich

References (7)
  1. Wechalekar A, Gillmore J, Hawkins P. Systemic amyloidosis. The Lancet. 2016; 387(10038): 2641–2654.
  2. Ruzicka T, Bruch-Gerharz D. Skrobiawice i hialinozy. In: Burgdorf WHC, Plewig G, Wolff HH, Landthaler M. ed. Braun-Falco Dermatologia. Tom 4. Wydawnictwo Czelej, Lublin 2017: 1275–1284.
  3. Myślak M, Mazurkiewicz J. Amyloidoza nerek. Algorytm dla nefrologa. Forum Nefrol. 2017; 10: 100–107.
  4. Hazenberg B. Amyloidosis. Rheum Dis Clin North Am. 2013; 39(2): 323–345.
  5. Pepys M. Amyloidosis. Ann Rev Med. 2006; 57: 223–41.
  6. Desport E, Bridoux F, Sirac C, et al. Centre national de référence pour l’amylose AL et les autres maladies par dépôts d’immunoglobulines monoclonales. Al amyloidosis. Orphanet J Rare Dis. 2012; 7: 54.
  7. Westermark GT, Fändrich M, Westermark P. AA amyloidosis: pathogenesis and targeted therapy. Annu Rev Pathol. 2015; 10: 321–344.

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