Renal Amyloidosis Secondary to Dystrophic Epidermolysis Bullosa: A Case Report and Review of Literature

被引：0

作者：

Atas, Dilek Barutcu ^{[1
]}

Aykent, Mahmut Basar ^{[1
]}

Arikan, Izzet Hakki ^{[1
]}

Asicioglu, Ebru ^{[1
]}

Velioglu, Arzu ^{[1
]}

Filinte, Deniz ^{[2
]}

Koc, Mehmet ^{[1
]}

Tuglular, Zubeyde Serhan ^{[1
]}

Ozener, Ishak Cetin ^{[1
]}

机构：

[1] Marmara Univ, Sch Med, Dept Internal Med, Div Nephrol, Istanbul, Turkey

[2] Marmara Univ, Sch Med, Dept Pathol, Istanbul, Turkey

来源：

TURKISH JOURNAL OF NEPHROLOGY | 2020年 / 29卷 / 04期

关键词：

Amyloidosis; dystrophic epidermolysis bullosa; nephrotic syndrome; SQUAMOUS-CELL CARCINOMA; PULMONARY;

D O I：

10.5152/turkjnephrol.2020.4195

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Dystrophic epidermolysis bullosa (DEB) is a rare and severe hereditary dermatosis, associated with collagen VII deficiency. A chronic inflammatory syndrome secondary to recurrent cutaneous infections may be responsible for amyloid deposition in this patient population, causing renal amyloidosis. Amyloidosis should be included in the differential diagnosis of DEB patients presenting with edema and proteinuria. Herein, we report a case of DEB complicated by squamous cell carcinoma and amyloid A amyloidosis of the kidneys confirmed with renal biopsy.

引用

页码：322 / 325

页数：4

共 14 条

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