原发性肝淀粉样变合并多发性骨髓瘤引起急性肝衰竭1例报告

Q4 Medicine Jordan Medical Journal Pub Date : 2022-08-24 DOI:10.35516/jmj.v56i3.360
Awni T. Abu Sneineh, Sara Haj Ali, T. Tamimi, Eman Alshebli, Reem Rajab, T. Dada, Deema Rayyan, Y. Rayyan
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引用次数: 0

摘要

原发性淀粉样变性是最常见的淀粉样变性类型,通常由浆细胞病变引起。它更常见的表现是累及肾脏和心脏,虽然原发性淀粉样变常累及肝脏,但很少引起临床明显的疾病。最常见的肝脏受累形式是肝肿大和碱性磷酸酶轻度升高。诊断需要组织活检显示刚果红染色阳性,治疗是理想的化疗和造血细胞移植的结合。肝淀粉样变合并肝功能衰竭的预后较差。在这里,我们报告一个致命的病例原发性淀粉样变在多发性骨髓瘤的设置在一个54岁的男子谁提出了急性肝功能衰竭。
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Primary Hepatic Amyloidosis Associated with Multiple Myeloma Causing Acute Liver Failure: A Case Report
Primary amyloidosis is the most prevalent type of amyloidosis and is usually due to plasma cell dyscrasia. It more commonly presents with renal and cardiac involvement and, although the liver is frequently involved in primary amyloidosis, it rarely causes clinically apparent disease. The most common form of hepatic involvement is hepatomegaly and mild elevation of alkaline phosphatase. Diagnosis requires tissue biopsy that demonstrates positive staining for Congo red and treatment is ideally a combination of chemotherapy and hematopoietic cell transplantation. The prognosis of hepatic amyloidosis associated with liver failure is poor. Here, we report a fatal case of primary amyloidosis in the setting of multiple myeloma in a 54-year-old man who presented with acute liver failure.
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来源期刊
Jordan Medical Journal
Jordan Medical Journal Medicine-Medicine (all)
CiteScore
0.20
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0.00%
发文量
33
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