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.
引用
收藏
页数:6
相关论文
共 21 条
  • [1] Molecular basis and inheritance patterns of amyloidosis cutis dyschromica
    Chiu, F. P. C.
    Wessagowit, V.
    Cakmak, M. F.
    Doolan, B. J.
    Kootiratrakarn, T.
    Chaowalit, P.
    Bunnag, T.
    Simpson, M. A.
    McGrath, J. A.
    Onoufriadis, A.
    [J]. CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2020, 45 (05) : 650 - 653
  • [2] Amyloidosis cutis dyschromica: a rare pigmentary disorder
    Garg, Taru
    Chander, Ram
    Jabeen, Masarat
    Barara, Meenu
    Mittal, Kanika
    Jain, Manjula
    Puri, Vandana
    [J]. JOURNAL OF CUTANEOUS PATHOLOGY, 2011, 38 (10) : 823 - 826
  • [3] Amyloidosis cutis dyschromica treated with acitretin. A case report
    Hennessy, Kerry
    Kim, Anna
    Rodriguez-Waitkus, Paul
    Morey, Gabriel
    Seminario-Vidal, Lucia
    [J]. DERMATOLOGIC THERAPY, 2020, 33 (06)
  • [4] In vivo Diagnosis of Primary Cutaneous Amyloidosis -The Role of Reflectance Confocal Microscopy
    Ionescu, Ana-Maria
    Ilie, Mihaela-Adriana
    Chitu, Virginia
    Razvan, Andrei
    Lixandru, Daniela
    Tanase, Cristiana
    Boda, Daniel
    Caruntu, Constantin
    Zurac, Sabina
    [J]. DIAGNOSTICS, 2019, 9 (03)
  • [5] Amyloidosis Cutis Dyschromica, a Rare Cause of Hyperpigmentation: a New Case and Literature Review
    Kuseyri, Oya
    Haas, Dorothea
    Lang, Nina
    Schaekel, Knut
    Bettendorf, Markus
    [J]. PEDIATRICS, 2017, 139 (05)
  • [6] Kutlu Omer, 2019, Dermatol Online J, V25
  • [7] Reflectance confocal microscopy for the characterization of primary cutaneous amyloidosis: a pilot study
    Lei, W.
    Ai-E, X.
    [J]. SKIN RESEARCH AND TECHNOLOGY, 2017, 23 (03) : 441 - 443
  • [8] A rare type of primary cutaneous amyloidosis: amyloidosis cutis dyschromica
    Madarasingha, N. P.
    Satgurunathan, K.
    de Silva, M. V. C.
    [J]. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2010, 49 (12) : 1416 - 1418
  • [9] Amyloidosis cutis dyschromica in two siblings and review of the epidemiology, clinical features and management in 48 cases
    Mahon, Caroline
    Oliver, Fergus
    Purvis, Diana
    Agnew, Karen
    [J]. AUSTRALASIAN JOURNAL OF DERMATOLOGY, 2016, 57 (04) : 307 - 311
  • [10] AMYLOIDOSIS-CUTIS-DYSCHROMICA - DNA-REPAIR REDUCTION IN THE CELLULAR-RESPONSE TO UV-LIGHT
    MORIWAKI, S
    NISHIGORI, C
    HORIGUCHI, Y
    IMAMURA, S
    TODA, K
    TAKEBE, H
    [J]. ARCHIVES OF DERMATOLOGY, 1992, 128 (07) : 966 - 970