First report of Mal de Meleda with pseudo-ainhum treated with gabapentin in a 17-year-old Chinese girl.
作者信息
Zhou Weinan, Zhang Zhen, Zhang Jia, Yao Zhirong
机构信息
Department of Dermatology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Institute of Dermatology, Shanghai Jiaotong University School of Medicine, Shanghai, China.
出版信息
Australas J Dermatol. 2021 Aug;62(3):e466-e468. doi: 10.1111/ajd.13625. Epub 2021 May 13.
PMID:33984155
Abstract
摘要
相似文献
1
First report of Mal de Meleda with pseudo-ainhum treated with gabapentin in a 17-year-old Chinese girl.17岁中国女孩患伴有假自发性断指症的梅勒达病，用加巴喷丁治疗的首例报告。
Australas J Dermatol. 2021 Aug;62(3):e466-e468. doi: 10.1111/ajd.13625. Epub 2021 May 13.
2
Mal de Meleda Palmoplantar Keratoderma with Pseudoainhum.伴有假性断指的梅勒达掌跖角化病
Skinmed. 2021 Oct 1;19(5):383-384. eCollection 2021.
3
Novel p.Ala675Thr missense mutation in TRPV3 in Olmsted syndrome.奥尔姆斯特德综合征中TRPV3基因的新型p.Ala675Thr错义突变。
Clin Exp Dermatol. 2020 Aug;45(6):796-798. doi: 10.1111/ced.14228. Epub 2020 May 14.
4
Mal de Meleda without mutations in the ARS coding sequence.无ARS编码序列突变的梅勒达病
Eur J Dermatol. 2002 Mar-Apr;12(2):129-32.
5
Mal de Meleda: recessive transgressive palmoplantar keratoderma with three unusual facultative features.梅勒达病：隐性过度性掌跖角化病，具有三种不寻常的兼性特征。
Dermatology. 1992;184(1):78-82. doi: 10.1159/000247506.
6
Successful treatment of keratoderma hereditaria mutilans with an aromatic retinoid.芳香维甲酸成功治疗遗传性残毁性角化病
Arch Dermatol. 1981 Apr;117(4):225-8. doi: 10.1001/archderm.117.4.225.
7
[Mal de Meleda. 16 cases].[梅勒达病。16例]
Tunis Med. 2006 Jul;84(7):423-6.
8
[Ainhum and "African acral keratoderma": three cases].[阿洪病与“非洲肢端角化病”：三例]
Ann Dermatol Venereol. 2015 Mar;142(3):170-5. doi: 10.1016/j.annder.2014.11.013. Epub 2015 Jan 23.
9
Hanging on by a thread: a rare case of secondary pseudoainhum.危在旦夕：一例罕见的继发性自发性断指（趾）病例
BMJ Case Rep. 2016 Feb 2;2016:bcr2015213854. doi: 10.1136/bcr-2015-213854.
10
[Acral melanoma in a patient with hereditary keratoderma of the palms and soles (mal de Meleda): A chance association?].[一名患有掌跖遗传性角化病（梅勒达病）患者的肢端黑色素瘤：偶然关联？]
Ann Dermatol Venereol. 2019 Nov;146(11):730-736. doi: 10.1016/j.annder.2019.08.013. Epub 2019 Sep 30.
引用本文的文献
1
A Case of Palmoplantar Keratodermas Complicated by Pseudoainhum and Literature Review.1例并发假性断肢的掌跖角化病病例及文献复习
Clin Cosmet Investig Dermatol. 2025 Jul 31;18:1827-1831. doi: 10.2147/CCID.S534631. eCollection 2025.
2
Identification of a novel compound heterozygous mutation and a homozygous mutation of SLURP1 in Chinese families with Mal de Meleda.鉴定马拉色菌毛囊炎中国家系中 SLURP1 的一个新的复合杂合突变和一个纯合突变。
BMC Med Genomics. 2023 Jul 1;16(1):152. doi: 10.1186/s12920-023-01580-1.
3
Case Report: Challenges in the Diagnosis of a Case of Mal de Meleda and a Therapeutic Attempt of Ixekizumab and Adalimumab.病例报告：一例梅勒达病诊断中的挑战以及使用司库奇尤单抗和阿达木单抗的治疗尝试
Front Med (Lausanne). 2022 Mar 10;9:821301. doi: 10.3389/fmed.2022.821301. eCollection 2022.
Zotero 插件