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Late Discovering Spina Ventosa: A Case Report

INTRODUCTION: Spina Ventosa is a rare condition that is easy to misdiagnose as other diseases. We present a case of late-diagnosed Spina Ventosa, which had not only the osteoarticular tuberculosis symptoms but also some severe symptoms, including pleural effusion, ascites, and anemia. By intensive t...

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Autores principales: Nguyen Ngoc, Sang, Nguyen Thai, Ha, Vu Van, Quang, Vu Tung, Lam, Nguyen Ngoc, Rang, Nguyen Van, Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273899/
https://www.ncbi.nlm.nih.gov/pubmed/34262359
http://dx.doi.org/10.2147/IMCRJ.S318003
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author Nguyen Ngoc, Sang
Nguyen Thai, Ha
Vu Van, Quang
Vu Tung, Lam
Nguyen Ngoc, Rang
Nguyen Van, Hung
author_facet Nguyen Ngoc, Sang
Nguyen Thai, Ha
Vu Van, Quang
Vu Tung, Lam
Nguyen Ngoc, Rang
Nguyen Van, Hung
author_sort Nguyen Ngoc, Sang
collection PubMed
description INTRODUCTION: Spina Ventosa is a rare condition that is easy to misdiagnose as other diseases. We present a case of late-diagnosed Spina Ventosa, which had not only the osteoarticular tuberculosis symptoms but also some severe symptoms, including pleural effusion, ascites, and anemia. By intensive treatment, our patient recovered completely. CASE REPORT: A 7-year-old boy was admitted with complaints of painless swelling of metacarpals, metatarsals, and phalanges of his hands and feet and a discharging sinus of the left toe. There was no family or past history of tuberculosis. His immunizations were up to date. General examination revealed that the child had pallor and was emaciated. No lymphadenopathy was detected. Investigations revealed hemoglobin: 74 g/l, and erythrocyte sedimentation rate (ESR) was 42 mm/hour. QuantiFERON-TB test was positive. The radiograph showed irregular swelling with sclerosis of the underlying bones. The right-hand x-ray showed cortical destruction, sclerosis, and cystic expansion or right second metacarpal. Chest x-ray indicated pleural effusion. Histopathological examination of specimen from the foot and lung and abdomen fluid confirmed tuberculosis. The child was treated with the first-line tuberculosis treatment regimen (Isoniazid, Rifampicin, Ethambutol, and Pyrazinamide) for two months, followed by Isoniazid, Rifampicin, and Pyrazinamide for a further four months. His lesions disappeared after six weeks of intensive treatment. CONCLUSION: A delay in diagnosis and treatment of tuberculosis can lead to systemic manifestations in multiple organs. Despite the delay in diagnosis, this child had a good outcome due to being treated promptly and adequately after the presentation.
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spelling pubmed-82738992021-07-13 Late Discovering Spina Ventosa: A Case Report Nguyen Ngoc, Sang Nguyen Thai, Ha Vu Van, Quang Vu Tung, Lam Nguyen Ngoc, Rang Nguyen Van, Hung Int Med Case Rep J Case Report INTRODUCTION: Spina Ventosa is a rare condition that is easy to misdiagnose as other diseases. We present a case of late-diagnosed Spina Ventosa, which had not only the osteoarticular tuberculosis symptoms but also some severe symptoms, including pleural effusion, ascites, and anemia. By intensive treatment, our patient recovered completely. CASE REPORT: A 7-year-old boy was admitted with complaints of painless swelling of metacarpals, metatarsals, and phalanges of his hands and feet and a discharging sinus of the left toe. There was no family or past history of tuberculosis. His immunizations were up to date. General examination revealed that the child had pallor and was emaciated. No lymphadenopathy was detected. Investigations revealed hemoglobin: 74 g/l, and erythrocyte sedimentation rate (ESR) was 42 mm/hour. QuantiFERON-TB test was positive. The radiograph showed irregular swelling with sclerosis of the underlying bones. The right-hand x-ray showed cortical destruction, sclerosis, and cystic expansion or right second metacarpal. Chest x-ray indicated pleural effusion. Histopathological examination of specimen from the foot and lung and abdomen fluid confirmed tuberculosis. The child was treated with the first-line tuberculosis treatment regimen (Isoniazid, Rifampicin, Ethambutol, and Pyrazinamide) for two months, followed by Isoniazid, Rifampicin, and Pyrazinamide for a further four months. His lesions disappeared after six weeks of intensive treatment. CONCLUSION: A delay in diagnosis and treatment of tuberculosis can lead to systemic manifestations in multiple organs. Despite the delay in diagnosis, this child had a good outcome due to being treated promptly and adequately after the presentation. Dove 2021-07-05 /pmc/articles/PMC8273899/ /pubmed/34262359 http://dx.doi.org/10.2147/IMCRJ.S318003 Text en © 2021 Nguyen Ngoc et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Case Report
Nguyen Ngoc, Sang
Nguyen Thai, Ha
Vu Van, Quang
Vu Tung, Lam
Nguyen Ngoc, Rang
Nguyen Van, Hung
Late Discovering Spina Ventosa: A Case Report
title Late Discovering Spina Ventosa: A Case Report
title_full Late Discovering Spina Ventosa: A Case Report
title_fullStr Late Discovering Spina Ventosa: A Case Report
title_full_unstemmed Late Discovering Spina Ventosa: A Case Report
title_short Late Discovering Spina Ventosa: A Case Report
title_sort late discovering spina ventosa: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273899/
https://www.ncbi.nlm.nih.gov/pubmed/34262359
http://dx.doi.org/10.2147/IMCRJ.S318003
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