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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Misdiagnosis and diagnostic delay in non-paraneoplastic sensory neuronopathies

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Author(s):
Muro Martinez, Alberto Rolim [1] ; Ribeiro, Mayani Costa [1] ; de Lima, Fabricio Diniz [1] ; Martins Jr, Carlos Roberto ; Martins, Melina Pazian [2] ; Nucci, Anamarli [2] ; Franca Jr, Marcondes Cavalcante
Total Authors: 7
Affiliation:
[1] Univ Estadual Campinas, Dept Neurol, Serv Doencas Neuromusculares, Campinas, SP - Brazil
[2] Martins Jr, Jr., Carlos Roberto, Univ Estadual Campinas, Dept Neurol, Serv Doencas Neuromusculares, Campinas, SP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: Arquivos de Neuro-Psiquiatria; v. 77, n. 7, p. 451-455, JUL 2019.
Web of Science Citations: 1
Abstract

ABSTRACT Sensory neuronopathies (SN) are a group of peripheral nerve disorders characterized by multifocal non-length-dependent sensory deficits and sensory ataxia. Its recognition is essential not only for proper management but also to guide the etiological investigation. The uncommon SN clinical picture and its rarity set the conditions for the misdiagnosis and the diagnostic delay, especially in non-paraneoplastic SN. Therefore, our objectives were to characterize the diagnostic odyssey for non-paraneoplastic SN patients, as well as to identify possible associated factors. Methods We consecutively enrolled 48 non-paraneoplastic SN patients followed in a tertiary neuromuscular clinic at the University of Campinas (Brazil). All patients were instructed to retrieve their previous medical records, and we collected the data regarding demographics, disease onset, previous incorrect diagnoses made and the recommended treatments. Results There were 34 women, with a mean age at the diagnosis of 45.9 ± 12.2 years, and 28/48 (58%) of the patients were idiopathic. Negative sensory symptoms were the heralding symptoms in 25/48 (52%); these were asymmetric in 36/48 (75%) and followed a chronic course in 35/48 (73%). On average, it took 5.4 ± 5.3 years for SN to be diagnosed; patients had an average of 3.4 ± 1.5 incorrect diagnoses. A disease onset before the age of 40 was associated to shorter diagnosis delay (3.7 ± 3.4 vs. 7.8 ± 6.7 years, p = 0.01). Conclusions These results suggest that diagnostic delay and misdiagnosis are frequent in non-paraneoplastic SN patients. As in other rare conditions, increased awareness in all the healthcare system levels is paramount to ensure accurate diagnosis and to improve care of these patients. (AU)

FAPESP's process: 13/26410-0 - Clinical, immunological and neurophysiological characterization of sensory neuronopathies
Grantee:Alberto Rolim Muro Martinez
Support Opportunities: Scholarships in Brazil - Doctorate (Direct)