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hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers.
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.
Afiliação
  • Luigetti M; Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Neurologia, 00168 Roma, Italy.
  • Romozzi M; Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
  • Bisogni G; Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Neurologia, 00168 Roma, Italy.
  • Cardellini D; Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
  • Cavallaro T; Centro Clinico NEMO-Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Di Paolantonio A; Dipartimento di Neuroscienze, Biomedicina e Scienze del Movimento, Università di Verona, 37134 Verona, Italy.
  • Fabrizi GM; Dipartimento di Neuroscienze, Biomedicina e Scienze del Movimento, Università di Verona, 37134 Verona, Italy.
  • Fenu S; Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
  • Gentile L; Dipartimento di Neuroscienze, Biomedicina e Scienze del Movimento, Università di Verona, 37134 Verona, Italy.
  • Grandis M; Rare Neurodegenerative and Neurometabolic Diseases Unit, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.
  • Marucci G; Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.
  • Massucco S; Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno Infantili (DINOGMI), Università degli studi di Genova, 16132 Genova, Italy.
  • Mazzeo A; IRCCS San Martino, 16132 Genova, Italy.
  • Pareyson D; Neuropathology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.
  • Romano A; Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno Infantili (DINOGMI), Università degli studi di Genova, 16132 Genova, Italy.
  • Russo M; Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.
  • Schenone A; Rare Neurodegenerative and Neurometabolic Diseases Unit, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.
  • Tagliapietra M; Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
  • Tozza S; Centro Clinico NEMO-Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Vita G; Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.
  • Sabatelli M; Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno Infantili (DINOGMI), Università degli studi di Genova, 16132 Genova, Italy.
Brain Sci ; 10(11)2020 Oct 26.
Article em En | MEDLINE | ID: mdl-33114611
ABSTRACT
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. Patients and

Methods:

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 (TTR) mutations. Sural nerve biopsy was performed according to standard protocols.

Results:

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.

Conclusions:

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.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2020 Tipo de documento: Article