Diagnostic sensitivity of abdominal fat aspiration in cardiac amyloidosis

被引:153
作者
Quarta, Candida Cristina [1 ,2 ]
Gonzalez-Lopez, Esther [3 ]
Gilbertson, Janet A. [1 ]
Botcher, Nichola [1 ]
Rowczenio, Dorota [1 ]
Petrie, Aviva [4 ]
Rezk, Tamer [1 ]
Youngstein, Taryn [1 ]
Mahmood, Shameem [1 ]
Sachchithanantham, Sajitha [1 ]
Lachmann, Helen J. [1 ]
Fontana, Marianna [1 ]
Whelan, Carol J. [1 ]
Wechalekar, Ashutosh D. [1 ]
Hawkins, Philip N. [1 ]
Gillmore, Julian D. [1 ]
机构
[1] UCL, Royal Free Hosp, Div Med, Natl Amyloidosis Ctr, Rowland Hill St, London NW3 2PF, England
[2] Alma Mater Studiorum Univ Bologna, Ist Cardiol, Dipartimento Med Specialist Diagnost & Sperimenta, Via Massarenti 9, I-40100 Bologna, Italy
[3] Hosp Univ Puerta de Hierro Majadahonda, Dept Cardiol, Heart Failure & Inherited Cardiac Dis Unit, Manuel de Falla 1, Madrid 28222, Spain
[4] UCL, Eastman Dent Inst, 256 Grays Inn Rd, London WC1X 8LD, England
关键词
Amyloid; Amyloidosis; Cardiomyopathy; Diagnosis; Fat aspiration; Scintigraphy; SYSTEMIC AMYLOIDOSIS; BIOPSY; POLYNEUROPATHY; SCINTIGRAPHY; AL;
D O I
10.1093/eurheartj/ehx047
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Congo red staining of an endomyocardial biopsy is the diagnostic gold-standard in suspected cardiac amyloidosis (CA), but the procedure is associated with the risk, albeit small, of serious complications, and delay in diagnosis due to the requirement for technical expertise. In contrast, abdominal fat pad fine needle aspiration (FPFNA) is a simple, safe and well-established procedure in systemic amyloidosis, but its diagnostic sensitivity in patients with suspected CA remains unclear. Methods and results We assessed the diagnostic sensitivity of FPFNA in 600 consecutive patients diagnosed with CA [216 AL amyloidosis, 113 hereditary transthyretin (ATTRm), and 271 wild-type transthyretin (ATTRwt) amyloidosis] at our Centre. Amyloid was detected on Congo red staining of FPFNAs in 181/216 (84%) patients with cardiac AL amyloidosis, including 100, 97, and 78% of those with a large, moderate, and small whole-body amyloid burden, respectively, as assessed by serum amyloid P (SAP) component scintigraphy (P < 0.001); the deposits were successfully typed as AL by immunohistochemistry in 102/216 (47%) cases. Amyloid was detected in FPFNAs of 51/113 (45%) patients with ATTRm CA, and only 42/271 (15%) cases with ATTRwt CA. Conclusions FPFNA has reasonable diagnostic sensitivity in cardiac AL amyloidosis, particularly in patients with a large whole-body amyloid burden. Although the diagnostic sensitivity of FPFNA is substantially lower in transthyretin CA, particularly ATTRwt, it may nevertheless sometimes obviate the need for endomyocardial biopsy.
引用
收藏
页码:1905 / 1908
页数:4
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