دوره 11، شماره 3 - ( 3-1399 )                   جلد 11 شماره 3 صفحات 342-340 | برگشت به فهرست نسخه ها


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Rafiei R, Eftekhari H, Rafiee B. Cutaneous amyloidosis as the first presentation of Waldenstrom macroglobulinemia. Caspian J Intern Med 2020; 11 (3) :340-342
URL: http://caspjim.com/article-1-1822-fa.html
Cutaneous amyloidosis as the first presentation of Waldenstrom macroglobulinemia. . 1399; 11 (3) :340-342

URL: http://caspjim.com/article-1-1822-fa.html


چکیده:   (3855 مشاهده)
Background: Waldenstrom macroglobulinemia is a lymphoplasmacytic lymphoma with elevated serum immunoglobulin M and multi-organ involvement. Primary systemic amyloidosis usually develops due to immunoglobulin light chains depositions in different organs due to an underlying gammopathy.
Case presentation: Our patient was an 86-year-old man with macroglossia, ecchymotic patches and bullous lesions associated with a skin laxity on the periorbital, palmar, and glans penis areas. Skin biopsy confirmed dermal amyloid depositions. In serum immunofixation electrophoresis, prominent monoclonal immunoglobulin-M lambda light chains were detected associated with prominent lymphoplasmacytic infiltration in bone marrow biopsy which was diagnosed as Waldenstrom macroglobulinemia.
Conclusion: Skin involvement presenting as cutaneous amyloidosis could be the first manifestation of Waldenstrom macroglobulinemia. We should think about an underlying gammopathy in an old patient with skin laxity and ecchymosis.
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نوع مطالعه: case report | موضوع مقاله: Dermathology
دریافت: 1398/1/4 | پذیرش: 1398/4/19 | انتشار: 1399/3/1

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