Unusual brain images of a boy with adolescent cerebral X-linked adrenoleukodystrophy presenting with exhibitionism: A CARE-compliant case report

被引:3
|
作者
Zheng, Feixia
Lin, Zhongdong
Ye, Xiuyun
Shi, Xulai
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Pediat Neurol, Wenzhou, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Zhejiang, Peoples R China
关键词
adolescence; basal ganglia; exhibitionism; thalamus; X-linked adrenoleukodystrophy; IMAGING MANIFESTATIONS; WHITE-MATTER; FOLLOW-UP; LEUKODYSTROPHIES; DISORDERS; DIAGNOSIS; VARIANT; GENE; ALD;
D O I
10.1097/MD.0000000000009481
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale:The respective involvements of both the thalamus and exhibitionism in cerebral X-linked adrenoleukodystrophy (X-ALD) have not been reported.Patient concerns:An 11-year-old boy initially presented with exhibitionism and progressive neurobehavioral symptoms. He subsequently developed transient urinary and fecal incontinence, and an unwillingness to eat or communicate.Diagnoses:We conducted contrast-enhanced brain magnetic resonance imaging (MRI), which revealed symmetrical altered signal intensities in bilateral frontal white matter, the basal ganglia, and dorsal thalami, as well as a peripheral rim of contrast enhancement. Diagnosis of adolescent cerebral X-ALD was confirmed on the basis of next generation genetic sequencing analysis.Interventions:We initiated the patient on hormonal replacement therapy.Outcomes:We observed rapidly progressive neurologic deterioration in this patient, and the boy fell into a vegetative state 10 months after discharge.Lessons:We recommend that physicians should not disregard X-ALD in patients with isolated psychiatric symptoms, including hypersexual behavior. The combination of detailed clinical evaluation, MRI, and next generation genetic sequencing can expedite the diagnostic process of atypical variant of X-ALD.
引用
收藏
页数:4
相关论文
共 50 条
  • [21] A novel missense mutation in the ABCD1 gene of a Chinese boy diagnosed with X-linked adrenoleukodystrophy: case report
    Mengqi Zhang
    Shupeng Shi
    Haoran Zhang
    Lihui Liu
    Linchao Wu
    Bo Xiao
    Weiping Liu
    Neurological Sciences, 2019, 40 : 1093 - 1096
  • [22] A novel missense mutation in the ABCD1 gene of a Chinese boy diagnosed with X-linked adrenoleukodystrophy: case report
    Zhang, Mengqi
    Shi, Shupeng
    Zhang, Haoran
    Liu, Lihui
    Wu, Linchao
    Xiao, Bo
    Liu, Weiping
    NEUROLOGICAL SCIENCES, 2019, 40 (05) : 1093 - 1096
  • [23] Cerebral childhood and adolescent X-linked adrenoleukodystrophy. Clinical presentation, neurophysiological, neuroimaging and biochemical investigations
    Zgorzalewicz-Stachowiak, Malgorzata
    Stradomska, Teresa Joanna
    Bartkowiak, Zuzanna
    Galas-Zgorzalewicz, Bozena
    FOLIA NEUROPATHOLOGICA, 2006, 44 (04) : 319 - 326
  • [24] X-Linked Juvenile Retinoschisis Presenting with Rhegmatogenous Retinal Detachment in a Male Nigerian Adolescent: A Case Report
    Babalola, Yewande O.
    Ibiyemi, Abisola A.
    Oluseye, Moteniola O.
    NIGERIAN POSTGRADUATE MEDICAL JOURNAL, 2022, 29 (03) : 278 - 280
  • [25] Case report of dysregulation of primary bile acid synthesis in a family with X-linked adrenoleukodystrophy
    Platek, Teresa
    Orso, Evelyn
    Zapala, Barbara
    Polus, Anna
    Kiec-Wilk, Beata
    Piwowar, Monika
    Chojnacka, Monika
    Cialowicz, Urszula
    Malczewska-Malec, Malgorzata
    Schmitz, Gerd
    Solnica, Bogdan
    Dembinska-Kiec, Aldona
    MEDICINE, 2018, 97 (49)
  • [26] A CARE-compliant article: A case report of unusual eschar and extensive soft tissue necrosis in Tsutsugamushi disease
    Byeon, Je Yeon
    Kim, Hyun
    Lee, Da Woon
    Choi, Hwan Jun
    MEDICINE, 2023, 102 (45) : E36009
  • [27] Treating adolescent pseudomyopia and elevated intraocular pressure using chiropractic and moxibustion: A CARE-compliant case report
    Fang, Yiyan
    Li, Zengtu
    Hu, Hantong
    Ye, Ziyu
    MEDICINE, 2024, 103 (11) : E37564
  • [28] X-linked agammaglobulinemia presenting with pseudomonas skin abscesses: A case report
    Guler, T.
    Emiroglu, M.
    Duymus, F.
    Ozdemir, E. M.
    Artac, H.
    ALLERGY, 2021, 76 : 156 - 156
  • [29] ENTHESOPATHY AS THE PRESENTING FEATURE OF X-LINKED HYPOPHOSPHATEMIA - A CASE-REPORT
    CHALMERS, J
    ACTA ORTHOPAEDICA SCANDINAVICA, 1993, 64 (02): : 221 - 223
  • [30] X-Linked Agammaglobulinemia Presenting with Secondary Hemophagocytic Syndrome: A Case Report
    Ozturk, Can
    Sutcuoglu, Sumer
    Atabay, Berna
    Berdeli, Afig
    CASE REPORTS IN MEDICINE, 2013, 2013