Subscribe to RSS

DOI: 10.1055/s-0042-1756638
O número relativo de linfócitos é menor quando o agente etiológico da doença de Pott é isolado com sucesso[*]
Article in several languages: português | English
Resumo
Objetivo Descrever as características clínico-epidemiológicas, laboratoriais e radiológicas da espondilodiscite tuberculosa na população brasileira e avaliar se há diferenças entre pacientes em que o agente etiológico da doença de Pott foi isolado ou não.
Métodos Os pacientes diagnosticados com tuberculose (TB) da coluna (doença de Pott) foram acompanhados em um hospital quaternário entre 2009 e 2019 e divididos em 2 grupos: isolamento positivo (IP) do agente etiológico (por baciloscopia, cultura ou teste rápido molecular positivo) e isolamento negativo (IN) do agente etiológico.
Resultados De um total de 26 pacientes com diagnóstico de TB da coluna, 21 (80,7%) eram do sexo masculino, e a média de idade era de 40 ± 22,5 anos. As contagens médias de linfócitos foram maiores no grupo IN (25,35 ± 13,08; p = 0,025) do que no grupo IP (14,18 ± 7,48). Além disso, a relação monócito/linfócito foi menor no grupo IN (0,39 ± 0,22; p = 0,009) do que no grupo IP (0,89 ± 0,65). O número relativo de linfócitos maior ou igual a 16,7 teve sensibilidade de 76,9% e especificidade de 62,5% no grupo IN. A razão monócito/linfócito maior ou igual a 0,58 teve sensibilidade de 84,6% e especificidade de 75,0% no grupo IN.
Conclusão Não observamos diferenças em relação às características clínico-epidemiológicas e radiológicas entre os dois grupos experimentais. No entanto, o grupo IN apresentou maior número de linfócitos e menor razão monócito/linfócito.
Suporte Financeiro
Não houve apoio financeiro de fontes públicas, comerciais ou sem fins lucrativos.
* Trabalho desenvolvido no Grupo de Afecções da Coluna Vertebral, Departamento de Ortopedia e Traumatologia, Santa Casa de Misericórdia de São Paulo, São Paulo, SP, Brasil.
Publication History
Received: 26 October 2021
Accepted: 18 July 2022
Article published online:
24 March 2023
© 2023. Sociedade Brasileira de Ortopedia e Traumatologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
-
Referências
- 1
Qian J,
Rijiepu A,
Zhu B,
Tian D,
Chen L,
Jing J.
Outcomes of radical debridement versus no debridement for the treatment of thoracic
and lumbar spinal tuberculosis. Int Orthop 2016; 40 (10) 2081-2088
MissingFormLabel
- 2
Wang G,
Dong W,
Lan T.
et al.
Diagnostic accuracy evaluation of the conventional and molecular tests for Spinal
Tuberculosis in a cohort, head-to-head study. Emerg Microbes Infect 2018; 7 (01) 109
MissingFormLabel
- 3
Dean A,
Zyck S,
Toshkezi G,
Galgano M,
Marawar S.
Challenges in the Diagnosis and Management of Spinal Tuberculosis: Case Series. Cureus
2019; 11 (01) e3855
MissingFormLabel
- 4
Dunn RN,
Ben Husien M.
Spinal tuberculosis: review of current management. Bone Joint J 2018; 100-B (04) 425-431
MissingFormLabel
- 5
Chen CH,
Chen YM,
Lee CW,
Chang YJ,
Cheng CY,
Hung JK.
Early diagnosis of spinal tuberculosis. J Formos Med Assoc 2016; 115 (10) 825-836
MissingFormLabel
- 6
BRASIL Ministério da Saúde.
Manual de recomendações para o controle da Tuberculose no Brasil. 2019 ;(61). Disponível
em: http://bvsms.saude.gov.br/bvs/publicacoes/manual_recomendacoes_controle_tuberculose_brasil.pdf
MissingFormLabel
- 7
Kilborn T,
Janse van Rensburg P,
Candy S.
Pediatric and adult spinal tuberculosis: imaging and pathophysiology. Neuroimaging
Clin N Am 2015; 25 (02) 209-231
MissingFormLabel
- 8
Uppal SS,
Tewari SC,
Verma S,
Dhot PS.
Comparison of CD4 and CD8 lymphocyte counts in HIV-negative pulmonary TB patients
with those in normal blood donors and the effect of antitubercular treatment: hospital-based
flow cytometric study. Cytometry B Clin Cytom 2004; 61 (01) 20-26
MissingFormLabel
- 9
Jones BE,
Oo MM,
Taikwel EK.
et al.
CD4 cell counts in human immunodeficiency virus-negative patients with tuberculosis.
Clin Infect Dis 1997; 24 (05) 988-991
MissingFormLabel
- 10
Couto BB,
Umeta RSG,
Caffaro MFS,
Meves R,
Landim E,
Avanzi O.
Análise radiológica comparativa entre espondilodiscite tuberculosa e inespecífica.
Coluna/Columna 2010; 9 (04) 394-400
MissingFormLabel
- 11
Rivas-Garcia A,
Sarria-Estrada S,
Torrents-Odin C,
Casas-Gomila L,
Franquet E.
Imaging findings of Pott's disease. Eur Spine J 2013; 22 (Suppl. 04) 567-578
MissingFormLabel
- 12
Kanna RM,
Babu N,
Kannan M,
Shetty AP,
Rajasekaran S.
Diagnostic accuracy of whole spine magnetic resonance imaging in spinal tuberculosis
validated through tissue studies. Eur Spine J 2019; 28 (12) 3003-3010
MissingFormLabel
- 13
Shi T,
Zhang Z,
Dai F.
et al.
Retrospective Study of 967 Patients With Spinal Tuberculosis. Orthopedics 2016; 39
(05) e838-e843
MissingFormLabel
- 14
Lee KY.
Comparison of pyogenic spondylitis and tuberculous spondylitis. Asian Spine J 2014;
8 (02) 216-223
MissingFormLabel
- 15
Durovni B,
Saraceni V,
van den Hof S.
et al.
Impact of replacing smear microscopy with Xpert MTB/RIF for diagnosing tuberculosis
in Brazil: a stepped-wedge cluster-randomized trial. PLoS Med 2014; 11 (12) e1001766
MissingFormLabel
- 16
Batirel A,
Erdem H,
Sengoz G.
et al.
The course of spinal tuberculosis (Pott disease): results of the multinational, multicentre
Backbone-2 study. Clin Microbiol Infect 2015; 21 (11) 1008.e9-1008.e18
MissingFormLabel
- 17
Nayak S,
Acharjya B.
VDRL test and its interpretation. Indian J Dermatol 2012; 57 (01) 3-8
MissingFormLabel
- 18
Rama Krishna M,
Gottam US,
Mahendra N.
Disseminated tuberculosis with severe immune thrombocytopenia. Respir Med Case Rep
2019; 27: 100812
MissingFormLabel
- 19
O'Shea MK,
Tanner R,
Müller J.
et al.
Immunological correlates of mycobacterial growth inhibition describe a spectrum of
tuberculosis infection. Sci Rep 2018; 8 (01) 14480
MissingFormLabel
- 20
Bashir AB,
Abufatima AS,
Mohamedani AA.
Impact of pulmonary tuberculosis on total and differential peripheral blood leukocytes
count. Int J Trop Med 2014; 9 (03) 33-37
MissingFormLabel
- 21
Liana P,
Brestilova B,
Yakub Rahadiyanto K.
The ratio of monocytes to lymphocytes accuracy as tuberculosis predictor. J Phys Conf
Ser 2019; 1246: 012024
MissingFormLabel
- 22
Djordjevic D,
Rondovic G,
Surbatovic M.
et al.
Neutrophil-to-Lymphocyte Ratio, Monocyte-to-Lymphocyte Ratio, Platelet-to-Lymphocyte
Ratio, and Mean Platelet Volume-to-Platelet Count Ratio as Biomarkers in Critically
Ill and Injured Patients: Which Ratio to Choose to Predict Outcome and Nature of Bacteremia?.
Mediators Inflamm 2018; 2018: 3758068
MissingFormLabel
- 23
Wang J,
Yin Y,
Wang X.
et al.
Ratio of monocytes to lymphocytes in peripheral blood in patients diagnosed with active
tuberculosis. Braz J Infect Dis 2015; 19 (02) 125-131
MissingFormLabel
- 24
La Manna MP,
Orlando V,
Dieli F.
et al.
Quantitative and qualitative profiles of circulating monocytes may help identifying
tuberculosis infection and disease stages. PLoS One 2017; 12 (02) e0171358
MissingFormLabel
- 25
Roy Chowdhury R,
Vallania F,
Yang Q.
et al.
A multi-cohort study of the immune factors associated with M. tuberculosis infection
outcomes. Nature 2018; 560 (7720): 644-648
MissingFormLabel
- 26
Jasenosky LD,
Scriba TJ,
Hanekom WA,
Goldfeld AE.
T cells and adaptive immunity to Mycobacterium tuberculosis in humans. Immunol Rev
2015; 264 (01) 74-87
MissingFormLabel
- 27
Cooper AM.
Cell-mediated immune responses in tuberculosis. Annu Rev Immunol 2009; 27: 393-422
MissingFormLabel
- 28
Monina L,
Khadera SA.
Chemokines in tuberculosis: The good, the bad and the ugly. Semin Immunol 2008; 23
(01) 1-7
MissingFormLabel