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Diagnosis and Treatment of Spinal Syphilitic Gumma: A Case Report

Neurosyphilis, which is caused by Treponema pallidum, is a rare sexually transmitted disease involving the central nervous system (CNS). Among all the sub-categories, spinal syphilitic gumma is extremely rare. In previous literature, limited cases of spinal syphilitic gumma have been reported, most...

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Autores principales: Cui, Linyang, Xu, Zushan, Hou, Hongjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974620/
https://www.ncbi.nlm.nih.gov/pubmed/32010040
http://dx.doi.org/10.3389/fneur.2019.01352
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author Cui, Linyang
Xu, Zushan
Hou, Hongjun
author_facet Cui, Linyang
Xu, Zushan
Hou, Hongjun
author_sort Cui, Linyang
collection PubMed
description Neurosyphilis, which is caused by Treponema pallidum, is a rare sexually transmitted disease involving the central nervous system (CNS). Among all the sub-categories, spinal syphilitic gumma is extremely rare. In previous literature, limited cases of spinal syphilitic gumma have been reported, most of which underwent surgery treatment. In this study, we reported a 46-year-old man, who presented with 5-day numbness of bilateral lower limbs, lower back pain, and irregular defecation. Magnetic resonance imaging (MRI) revealed a homogeneous peripheral enhancement and intramedullary nodule at the T7 level with extensive thoracic cord edema. Combining with laboratory examination results, the syphilitic gumma was considered. One month after the administration of penicillin G, the symptoms vanished. Six months later, MRI indicated no intramedullary nodule.
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spelling pubmed-69746202020-01-31 Diagnosis and Treatment of Spinal Syphilitic Gumma: A Case Report Cui, Linyang Xu, Zushan Hou, Hongjun Front Neurol Neurology Neurosyphilis, which is caused by Treponema pallidum, is a rare sexually transmitted disease involving the central nervous system (CNS). Among all the sub-categories, spinal syphilitic gumma is extremely rare. In previous literature, limited cases of spinal syphilitic gumma have been reported, most of which underwent surgery treatment. In this study, we reported a 46-year-old man, who presented with 5-day numbness of bilateral lower limbs, lower back pain, and irregular defecation. Magnetic resonance imaging (MRI) revealed a homogeneous peripheral enhancement and intramedullary nodule at the T7 level with extensive thoracic cord edema. Combining with laboratory examination results, the syphilitic gumma was considered. One month after the administration of penicillin G, the symptoms vanished. Six months later, MRI indicated no intramedullary nodule. Frontiers Media S.A. 2020-01-15 /pmc/articles/PMC6974620/ /pubmed/32010040 http://dx.doi.org/10.3389/fneur.2019.01352 Text en Copyright © 2020 Cui, Xu and Hou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Cui, Linyang
Xu, Zushan
Hou, Hongjun
Diagnosis and Treatment of Spinal Syphilitic Gumma: A Case Report
title Diagnosis and Treatment of Spinal Syphilitic Gumma: A Case Report
title_full Diagnosis and Treatment of Spinal Syphilitic Gumma: A Case Report
title_fullStr Diagnosis and Treatment of Spinal Syphilitic Gumma: A Case Report
title_full_unstemmed Diagnosis and Treatment of Spinal Syphilitic Gumma: A Case Report
title_short Diagnosis and Treatment of Spinal Syphilitic Gumma: A Case Report
title_sort diagnosis and treatment of spinal syphilitic gumma: a case report
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974620/
https://www.ncbi.nlm.nih.gov/pubmed/32010040
http://dx.doi.org/10.3389/fneur.2019.01352
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