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硬斑病中的癫痫发作:帕里-龙贝格综合征病例报告

Seizure in Morphea: A Case Report of Parry-Romberg Syndrome.

作者信息

S Veerasivabalan, Murugesan Hema, Ramanathan Kalpana, Selvaraj Chandrasekar

机构信息

Department of General Medicine, Stanley Medical College and Hospital, Chennai, IND.

Department of Rheumatology, Stanley Medical College and Hospital, Chennai, IND.

出版信息

Cureus. 2024 Jul 23;16(7):e65210. doi: 10.7759/cureus.65210. eCollection 2024 Jul.

DOI:10.7759/cureus.65210
PMID:39176365
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11340906/
Abstract

Parry-Romberg syndrome is a rare neurocutaneous disease characterized by progressive hemifacial atrophy. We present the case of a 14-year-old, a known case of linear morphea, who presented with seizure and on evaluation was diagnosed with Parry-Romberg syndrome. It causes a profound impact on aesthetic well-being and has a significant psychosocial morbidity. This case report aims to highlight the effective multidisciplinary team approach involving a rheumatologist, dermatologist, neurologist, and ophthalmologist which ultimately culminated in the meticulous management of the disease in our patient.

摘要

帕里-龙贝格综合征是一种罕见的神经皮肤疾病,其特征为进行性半侧面部萎缩。我们报告一例14岁已知线状硬皮病患者,该患者出现癫痫发作,经评估被诊断为帕里-龙贝格综合征。它对美观有深远影响,且具有显著的社会心理发病率。本病例报告旨在强调多学科团队的有效方法,该团队由风湿病学家、皮肤科医生、神经科医生和眼科医生组成,最终对我们的患者进行了精心的疾病管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/edb709d69bef/cureus-0016-00000065210-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/b00b67489556/cureus-0016-00000065210-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/28608f25219b/cureus-0016-00000065210-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/70d7c91dc7c2/cureus-0016-00000065210-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/6301a8e96593/cureus-0016-00000065210-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/edb709d69bef/cureus-0016-00000065210-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/b00b67489556/cureus-0016-00000065210-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/28608f25219b/cureus-0016-00000065210-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/70d7c91dc7c2/cureus-0016-00000065210-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/6301a8e96593/cureus-0016-00000065210-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db0/11340906/edb709d69bef/cureus-0016-00000065210-i05.jpg

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本文引用的文献

1
Late-onset Parry-Romberg Syndrome with atypical neurological manifestations: A case report.伴有非典型神经表现的迟发性帕里-龙贝格综合征:一例报告
Radiol Case Rep. 2023 Nov 17;19(1):459-463. doi: 10.1016/j.radcr.2023.10.032. eCollection 2024 Jan.
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Morphea: The 2023 update.硬斑病:2023年更新版
Front Med (Lausanne). 2023 Feb 13;10:1108623. doi: 10.3389/fmed.2023.1108623. eCollection 2023.
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Epilepsy in paediatric patients with Parry-Romberg syndrome: A review of the literature.患有帕里-龙贝格综合征的儿科患者的癫痫:文献综述
Seizure. 2020 Jan 28;76:89-95. doi: 10.1016/j.seizure.2020.01.017.
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Parry-Romberg syndrome in an adolescent: a case report on progressive hemifacial atrophy.青少年帕里-罗姆伯格综合征:一例进行性半侧面部萎缩病例报告
Oxf Med Case Reports. 2020 Jan 31;2020(1):omz127. doi: 10.1093/omcr/omz127. eCollection 2020 Jan.
5
Neurological Manifestations in Parry-Romberg Syndrome: 2 Case Reports.帕里-龙贝格综合征的神经学表现:2例病例报告。
Medicine (Baltimore). 2015 Jul;94(28):e1147. doi: 10.1097/MD.0000000000001147.
6
Parry Romberg Syndrome: 7 Cases and Literature Review.帕里-龙贝格综合征:7例病例及文献综述
AJNR Am J Neuroradiol. 2015 Jul;36(7):1355-61. doi: 10.3174/ajnr.A4297. Epub 2015 Jun 11.