Case Report: Amyloidosis Cutis Dyschromica: Dermoscopy and Reflectance Confocal Microscopy and Gene Mutation Analysis of a Chinese Pedigree

被引:4
作者
Wang, Hui [1 ,2 ,3 ,4 ,5 ]
Zhong, Zhenyu [1 ,2 ,3 ,4 ,5 ]
Wang, Xiuli [1 ,2 ,3 ,4 ,5 ]
Zheng, Liyun [1 ,2 ,3 ,4 ,5 ]
Wang, Yifan [1 ,2 ,3 ,4 ,5 ]
Wang, Shan [1 ,2 ,3 ,4 ,5 ]
Liu, Siqi [1 ,2 ,3 ,4 ,5 ]
Li, Hui [1 ,2 ,3 ,4 ,5 ]
Guo, Ze [1 ,2 ,3 ,4 ,5 ]
Gao, Min [1 ,2 ,3 ,4 ,5 ]
机构
[1] Anhui Med Univ, Hosp 1, Dept Dermatol, Hefei, Peoples R China
[2] Anhui Med Univ, Inst Dermatol, Hefei, Peoples R China
[3] Anhui Med Univ, Key Lab Dermatol, Minist Educ, Hefei, Peoples R China
[4] Anhui Prov Inst Translat Med, Hefei, Peoples R China
[5] Inflammat & Immune Mediated Dis Lab Anhui Prov, Hefei, Anhui, Peoples R China
关键词
amyloidosis cutis dyschromica; dermoscopy; reflectance confocal microscopy; non-invasive techniques; mutation; PRIMARY CUTANEOUS AMYLOIDOSIS;
D O I
10.3389/fmed.2021.774266
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Amyloidosis cutis dyschromica (ACD) is a rare type of primary localized cutaneous amyloidosis. Non-invasive techniques can provide important clues for early diagnosis.Objectives: To highlight the characteristic imaging changes of ACD under dermoscopy and reflectance confocal microscopy (RCM), investigate gene mutations in a Chinese Han pedigree of ACD, and analyze the genotype-phenotype correlation.Methods: Dermoscopy and RCM examinations were completed together for the pedigree, and the imaging characteristics were described. The diagnosis of ACD was confirmed by pathological examination. Sequencing was performed followed by bioinformatics and genotype-phenotype correlation. ACD-related articles published on PubMed between January 1970 and March 2021 were reviewed and summarized.Results: In ACD, dermoscopy showed patchy white hypopigmentation and brownish spots, stripes, or hyperpigmented blotches and patches. RCM showed a highly refractive substance with clumpy, dotted, and linear structures inside the papillary dermis. Sequencing identified glycoprotein non-metastatic melanoma protein B (GPNMB) missense mutations [c.393T>G (p.Y131X; NM_001005340.2)] and a frameshift deletion mutation [c.719_720delTG (p.V240fs; NM_001005340.2)]. The ANNOtate VARiation (ANNOVAR) software predicted that c.393T>G is a pathogenic mutation. The literature review found 14 mutations, namely, 5 (35.7%) frameshift mutations, 4 (28.6%) non-sense mutations, 4 (28.6%) missense mutations, and 1 (7.1%) splice site mutation. Blisters and epidermolysis were observed in several cases, but there was no significant association between clinical manifestations and mutations in ACD.Conclusions: This study was the first to combine dermoscopy and RCM to describe ACD. Two GPNMB gene mutations were reported in a Chinese ACD pedigree. The genotype-phenotype correlation was analyzed for the first time; however, there was no significant correlation.
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页数:6
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共 21 条
  • [11] Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica
    Onoufriadis, Alexandros
    Hsu, Chao-Kai
    Eide, Cindy R.
    Nanda, Arti
    Orchard, Guy E.
    Tomita, Kenji
    Sheriff, Adam
    Scott, William
    Tierney, Chloe
    Lee, John Y. W.
    Gomaa, Nesrin S.
    Desomchoke, Rasthawathana
    Lwin, Su M.
    Tu, Wei-Ting
    Chen, Liang-Yu
    Huang, Hsin-Yu
    Chao, Sheau-Chiou
    Lee, Julia Yu-Yun
    Bare, Yonis
    Hayday, Thomas
    Guy, Alyson L.
    Liu, Lu
    Lees, Chris
    Hirdler, Tessa
    Lovell, Patricia
    Xia, Lily
    Dayrit, Johannes F.
    Calonje, Eduardo
    Simpson, Michael A.
    Tolar, Jakub
    Parsons, Maddy
    McGrath, John A.
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2019, 139 (12) : 2550 - +
  • [12] Amyloidosis cutis dyschromica: A case treated with acitretin
    Ozcan, A
    Senol, M
    Aydin, NE
    Karaca, S
    [J]. JOURNAL OF DERMATOLOGY, 2005, 32 (06) : 474 - 477
  • [13] Amyloidosis cutis dyschromica
    Qiao, Jianjun
    Fang, Hong
    Yao, Hongtian
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2012, 7
  • [14] Two missense mutations in GPNMB cause autosomal recessive amyloidosis cutis dyschromica in the consanguineous pakistani families
    Rahman, Obaid Ur
    Kim, Jeena
    Mahon, Caroline
    Jelani, Musharraf
    Kang, Changsoo
    [J]. GENES & GENOMICS, 2021, 43 (05) : 471 - 478
  • [15] Three novel mutations in GPNMB in two pedigrees with amyloidosis cutis dyschromica
    Wang, J.
    Li, Y.
    Xing, L.
    Zhao, M.
    Zhang, S.
    Li, Z.
    Yao, Z.
    Li, M.
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 2019, 181 (06) : 1327 - 1329
  • [16] Case of amyloidosis cutis dyschromica with dermoscopy
    Wang, Lian
    Jiang, Xian
    Zhang, Nan
    Liu, Lian
    Zhou, Hui
    Liu, Hong-jie
    [J]. JOURNAL OF DERMATOLOGY, 2019, 46 (02) : E77 - E79
  • [17] Case Report: Diagnosis of Primary Cutaneous Amyloidosis Using Dermoscopy and Reflectance Confocal Microscopy
    Wang, Xiuli
    Wang, Hui
    Zhong, Zhenyu
    Zheng, Liyun
    Wang, Yifan
    Guo, Ze
    Li, Hui
    Gao, Min
    [J]. FRONTIERS IN MEDICINE, 2021, 7
  • [18] The first report of diagnosing of keratoacanthoma in Chinese Han patients using dermoscopy and reflectance confocal microscopy
    Wang, Xiuli
    Wang, Yifan
    Wang, Hui
    Zheng, Liyun
    Guo, Ze
    Fan, Xing
    Gao, Min
    [J]. SKIN RESEARCH AND TECHNOLOGY, 2021, 27 (03) : 422 - 427
  • [19] Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans
    Yang, Chi-Fan
    Lin, Shuan-Pei
    Chiang, Chien-Ping
    Wu, Yu-Hung
    H'ng, Weng Siong
    Chang, Chun-Ping
    Chen, Yuan-Tsong
    Wu, Jer-Yuarn
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2018, 102 (02) : 219 - 232
  • [20] Amyloidosis cutis dyschromica in two female siblings: cases report
    Yang, Wenlin
    Lin, Yangyang
    Yang, Jian
    Lin, Wensheng
    [J]. BMC DERMATOLOGY, 2011, 11