Have one's view of the important overshadowed by the trivial: chronic progressive external ophthalmoplegia combined with unilateral facial nerve injury: a case report and literature review

被引:0
作者
Feng, Ziyang [1 ]
Lai, Rui [2 ]
Wei, Jia [1 ,3 ]
Liu, Xuan [1 ,3 ]
Chen, Xueqin [1 ,3 ]
Liu, Yangsicheng [1 ]
Qin, Wenxin [1 ]
Qin, Xiude [1 ,3 ]
Kong, Fanxin [1 ,3 ]
机构
[1] Guangzhou Univ Chinese Med, Clin Med Coll 4, Shenzhen, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Sch Acupuncture & Tuina, Chengdu, Peoples R China
[3] Shenzhen Tradit Chinese Med Hosp, Dept Encephalopathy & Psychol, Shenzhen, Peoples R China
来源
FRONTIERS IN NEUROLOGY | 2024年 / 14卷
关键词
chronic progressive external ophthalmoplegia; case report; misdiagnosis; muscle biopsy; genetic testing; MITOCHONDRIAL-DNA DELETIONS; MUSCLE; DISEASE; MUTATION; REPEAT;
D O I
10.3389/fneur.2023.1268053
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic progressive external ophthalmoplegia (CPEO) is a mitochondrial encephalomyopathy that is characterized by progressive ptosis and impaired ocular motility. Owing to its nonspecific clinical manifestations, CPEO is often misdiagnosed as other conditions. Herein, we present the case of a 34-year-old woman who primarily presented with incomplete left eyelid closure and limited bilateral eye movements. During the 6-year disease course, she was diagnosed with myasthenia gravis and cranial polyneuritis. Finally, skeletal muscle tissue biopsy confirmed the diagnosis. Biopsy revealed pathological changes in mitochondrial myopathy. Furthermore, mitochondrial gene testing of the skeletal muscle revealed a single chrmM:8469-13447 deletion. In addition, we summarized the findings of 26 patients with CPEO/Kearns-Sayre syndrome who were misdiagnosed with other diseases owing to ocular symptoms. In conclusion, we reported a rare clinical case and emphasized the symptomatic diversity of CPEO. Furthermore, we provided a brief review of the diagnosis and differential diagnosis of the disease.
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页数:10
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共 43 条
  • [1] Optimizing Muscle Biopsy for the Diagnosis of Mitochondrial Myopathy
    Almousa, Radwan
    Charlton, Amanda
    Rajesh, Shruthi Tara
    Sundar, Gangadhara
    Amrith, Shantha
    [J]. OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY, 2009, 25 (05) : 366 - 370
  • [2] OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes
    Amati-Bonneau, Patrizia
    Valentino, Maria Lucia
    Reynier, Pascal
    Gallardo, Maria Esther
    Bornstein, Belen
    Boissiere, Anne
    Campos, Yolanda
    Rivera, Henry
    de la Aleja, Jesus Gonzalez
    Carroccia, Rosanna
    Iommarini, Luisa
    Labauge, Pierre
    Figarella-Branger, Dominique
    Marcorelles, Pascale
    Furby, Alain
    Beauvais, Katell
    Letournel, Franck
    Liguori, Rocco
    La Morgia, Chiara
    Montagna, Pasquale
    Liguori, Maria
    Zanna, Claudia
    Rugolo, Michela
    Cossarizza, Andrea
    Wissinger, Bernd
    Verny, Christophe
    Schwarzenbacher, Robert
    Martin, Miguel Angel
    Arenas, Joaquin
    Ayuso, Carmen
    Garesse, Rafael
    Lenaers, Guy
    Bonneau, Dominique
    Carelli, Valerio
    [J]. BRAIN, 2008, 131 : 338 - 351
  • [3] Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant
    Bacalhau, Mafalda
    Simoes, Marta
    Rocha, Mariana C.
    Hardy, Steven A.
    Vincent, Amy E.
    Duraes, Joao
    Macario, Maria C.
    Santos, Maria Joao
    Rebelo, Olinda
    Lopes, Carla
    Pratas, Joao
    Mendes, Candida
    Zuzarte, Monica
    Cristina Rego, A.
    Girao, Henrique
    Wong, Lee-Jun C.
    Taylor, Robert W.
    Grazina, Manuela
    [J]. NEUROMUSCULAR DISORDERS, 2018, 28 (04) : 350 - 360
  • [4] Update on Chronic Progressive External Ophthalmoplegia
    Bau, Viktoria
    Zierz, Stephan
    [J]. STRABISMUS, 2005, 13 (03) : 133 - 142
  • [5] PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND BENIGN RETINAL PIGMENTATION
    BECKERMAN, BL
    HENKIND, P
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1976, 81 (01) : 89 - 92
  • [6] Clinical, Histological, and Genetic Features of 25 Patients with Autosomal Dominant Progressive External Ophthalmoplegia (ad-PEO)/PEO-Plus Due to TWNK Mutations
    Bermejo-Guerrero, Laura
    de la Hoz, Carlos Pablo de Fuenmayor-fernandez
    Serrano-Lorenzo, Pablo
    Blazquez-Encinar, Alberto
    Gutierrez-Gutierrez, Gerardo
    Martinez-Vicente, Laura
    Galan-Davila, Lucia
    Garcia-Garcia, Jorge
    Arenas, Joaquin
    Muelas, Nuria
    Hernandez-Lain, Aurelio
    Dominguez-Gonzalez, Cristina
    Martin, Miguel A.
    [J]. JOURNAL OF CLINICAL MEDICINE, 2022, 11 (01)
  • [7] Selected Case From the Arkadi M. Rywlin International Pathology Slide Series Mitochondrial Myopathy Presenting With Chronic Progressive External Ophthalmoplegia (CPEO): A Case Report
    Bisceglia, Michele
    Crociani, Paola
    Fogli, Danilo
    Centola, Antonio
    Galliani, Carlos A.
    Pasquinelli, Gianandrea
    [J]. ADVANCES IN ANATOMIC PATHOLOGY, 2014, 21 (06) : 461 - 468
  • [8] CLINICAL-FEATURES OF MITOCHONDRIAL MYOPATHY
    BYRNE, E
    BLUMBERGS, PC
    HALLPIKE, JF
    MUKHERJEE, TM
    [J]. AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1983, 13 (04): : 353 - 358
  • [9] Calderon-Garciduenas AL., 2000, Rep Case Rev Liter Gaceta Medica de Mexico, V136, P267
  • [10] Mitochondrial disease mimicking polymyositis: A case report
    Corrado, A
    Cantatore, FP
    Serlenga, L
    Amati, A
    Petruzzella, V
    Lapadula, G
    [J]. CLINICAL RHEUMATOLOGY, 2002, 21 (05) : 411 - 414