Evidence map›Paper›PMID 41858772›Full record

ArticleExperimental and therapeutic medicine2026

A rare case of early-onset cerebral syphilitic gummata with severe neurological decline in early-stage syphilis: A case report.

Yujie Ji, Shelin Liu, Yunwei Wang, Youcai Zhao, Zheng Cai, Bing Li

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In one paragraph

Article in Experimental and therapeutic medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Yujie JiDepartment of Neurosurgery, Jiangnan University Medical Center, Jiangnan University, Wuxi, Jiangsu 214000, P.R. China.
Shelin LiuDepartment of Neurosurgery, Jiangnan University Medical Center, Jiangnan University, Wuxi, Jiangsu 214000, P.R. China.
Yunwei WangDepartment of Bioinformatics, School of Science, Xi'an Jiaotong-Liverpool University, Suzhou, Jiangsu 215000, P.R. China.
Youcai ZhaoDepartment of Pathology, Nanjing No. 1 People's Hospital, Nanjing, Jiangsu 210000, P.R. China.
Zheng CaiDepartment of Neurosurgery, Jiangnan University Medical Center, Jiangnan University, Wuxi, Jiangsu 214000, P.R. China.
Bing LiDepartment of Neurosurgery, Jiangnan University Medical Center, Jiangnan University, Wuxi, Jiangsu 214000, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral syphilitic gummata are rare granulomatous lesions associated with tertiary syphilis, typically developing several years after the initial infection. Early-stage syphilis with cerebral gummata and accompanying severe neurological symptoms is rare. Failure to recognize the lesions or delays in diagnosis may lead to marked and potentially irreversible central nervous system injury. In the present study, the case of a 60-year-old man with a 6-month history of syphilis who presented with progressive right-sided limb weakness and dysarthria is reported. Brain magnetic resonance imaging revealed multiple ring-enhancing lesions accompanied by extensive perilesional edema. Due to the severity of the symptoms and a notable mass effect, surgical intervention was performed to remove the gummatous lesion, followed by histopathological confirmation of syphilitic granuloma. The patient was subsequently treated with high-dose intravenous penicillin, which led to notable improvement in neurological function and resolution of the symptoms; follow-up imaging demonstrated no recurrence of intracranial lesions. In conclusion, the present case illustrates the importance of early recognition and a multidisciplinary approach in the management of neurosyphilis with cerebral gummata. Increased awareness of this rare presentation may facilitate a timely diagnosis and appropriate treatment in similar clinical scenarios.

Indexed as

case reportCSGearly-stage syphilisgranulomatous lesionsNS

Identifiers

PMID41858772
PMCPMC12997095

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