Luigetti Marco, Romozzi Marina, Bisogni Giulia, Cardellini Davide, Cavallaro Tiziana, Di Paolantonio Andrea, Fabrizi Gian Maria, Fenu Silvia, Gentile Luca, Grandis Marina, Marucci Gianluca, Massucco Sara, Mazzeo Anna, Pareyson Davide, Romano Angela, Russo Massimo, Schenone Angelo, Tagliapietra Matteo, Tozza Stefano, Vita Giuseppe, Sabatelli Mario
Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Neurologia, 00168 Roma, Italy.
Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
Brain Sci. 2020 Oct 26;10(11):780. doi: 10.3390/brainsci10110780.
Pathological evidence of amyloid on nerve biopsy has been the gold standard for diagnosis in hereditary transthyretin amyloidosis polyneuropathy (hATTR-PN) for a long time. In this article, we reviewed the pathological findings of a large series of sural nerve biopsies from a cohort of hATTR-PN patients, collected by different Italian referral centers. We reviewed clinical and pathological data from hATTR-PN patients, diagnosed and followed in five Italian referral centers for peripheral neuropathies. Diagnosis was formulated after a positive genetic test for transthyretin () mutations. Sural nerve biopsy was performed according to standard protocols. Sixty-nine sural nerve biopsies from hATTR-PN patients were examined. Congo red positive deposits were found in 73% of cases. Only the Phe64Leu mutation failed to show amyloid deposits in a high percentage of biopsies (54%), as already described. Unusual pathological findings, such as myelin abnormalities or inflammatory infiltrates, were detected in occasional cases. Even if no longer indicated to confirm hATTR-PN clinical suspicion, nerve biopsy remains, in expert hands, a rapid and inexpensive tool to detect amyloid deposition. In Italy, clinicians should be aware that a negative biopsy does not exclude hATTR-PN, particularly for Phe64Leu, one of the most frequent mutations in this country.
长期以来,神经活检中淀粉样蛋白的病理证据一直是遗传性转甲状腺素蛋白淀粉样变多发性神经病(hATTR-PN)诊断的金标准。在本文中,我们回顾了由不同意大利转诊中心收集的一大系列hATTR-PN患者腓肠神经活检的病理结果。我们回顾了在意大利五个外周神经病转诊中心诊断和随访的hATTR-PN患者的临床和病理数据。在转甲状腺素蛋白(TTR)突变基因检测呈阳性后做出诊断。腓肠神经活检按照标准方案进行。对69例hATTR-PN患者的腓肠神经活检进行了检查。73%的病例中发现刚果红阳性沉积物。正如之前所描述的,只有Phe64Leu突变在高比例(54%)的活检中未显示淀粉样沉积物。偶尔会检测到异常的病理结果,如髓鞘异常或炎性浸润。即使不再建议通过神经活检来证实hATTR-PN的临床怀疑,但在专家手中,神经活检仍然是一种快速且廉价的检测淀粉样蛋白沉积的工具。在意大利,临床医生应意识到活检结果为阴性并不排除hATTR-PN,特别是对于Phe64Leu这种该国最常见的突变之一。