Bullous Pemphigoid in X-linked Alport Syndrome

被引:2
|
作者
Yamawaki, Masahiro [1 ]
Katayama, Kan [1 ]
Fujimoto, Mika [1 ]
Goto, Hiroyuki [2 ]
Yuasa, Hiroto [3 ]
Kozuka, Yuji [3 ]
Mori, Mutsuki [1 ]
Takahashi, Daisuke [1 ]
Saiki, Ryosuke [1 ]
Hirabayashi, Yosuke [1 ]
Murata, Tomohiro [1 ]
Yamanaka, Keiichi [2 ]
Dohi, Kaoru [1 ]
机构
[1] Mie Univ, Dept Cardiol & Nephrol, Grad Sch Med, Tsu, Japan
[2] Mie Univ, Dept Dermatol, Grad Sch Med, Tsu, Japan
[3] Mie Univ Hosp, Dept Pathol, Tsu, Japan
关键词
basement membrane zone; bullous pemphigoid; X-linked Alport syndrome; SUBEPIDERMAL BLISTERS; COLLAGEN; IV; IDENTIFICATION; AUTOANTIBODIES; MUTATIONS; ALPHA-5;
D O I
10.2169/internalmedicine.0972-22
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Skin lesions in X-linked Alport syndrome (XLAS) are rarely observed. Bullous pemphigoid (BP) is caused by autoantibodies against BP180, also called & alpha;1 (XVII) chain, in the basement membrane zone (BMZ). A 48-year-old man with XLAS developed tense blisters. A skin biopsy showed a cleft between the basal cell layer and dermis, with the infiltration of neutrophils and eosinophils. & alpha;1 (XVII) staining was positive on the epidermal side of & alpha;2/5 (IV) staining. Oral prednisolone improved his symptoms gradually. Abundant tense blisters on the palms and soles might suggest an important role of the & alpha;5 (IV) chain in the integrity of BMZ.
引用
收藏
页码:2375 / 2379
页数:5
相关论文
共 50 条
  • [41] Genetic cause of X-linked Alport syndrome in a family of domestic dogs
    Melissa L. Cox
    George E. Lees
    Clifford E. Kashtan
    Keith E. Murphy
    Mammalian Genome, 2003, 14 : 396 - 403
  • [42] Gene expression analysis in a canine model of X-linked Alport syndrome
    Kimberly A. Greer
    Marnie A. Higgins
    Melissa L. Cox
    Timothy P. Ryan
    Brian R. Berridge
    Clifford E. Kashtan
    George E. Lees
    Keith E. Murphy
    Mammalian Genome, 2006, 17 : 976 - 990
  • [43] MOLECULAR AND IMMUNOLOGICAL STUDIES IN X-LINKED AND AUTOSOMAL RECESSIVE ALPORT SYNDROME
    SMEETS, HJ
    LEMMINK, HH
    VANDENHEUVEL, LP
    KLUIJTMANS, L
    SCHRODER, CH
    MOCHIZUKI, T
    ZHOU, J
    REEDERS, S
    TRYGGVASON, K
    MONNENS, L
    BRUNNER, HG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1230 - 1230
  • [44] The Value of Clinical Criteria in Identifying Patients with X-Linked Alport Syndrome
    Hanson, Helen
    Storey, Helen
    Pagan, Judith
    Flinter, Frances
    CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 6 (01): : 198 - 203
  • [45] IgA nephropathy in patient with X-linked Alport syndrome - a case report
    Horacek, M.
    Pavic, P.
    Senjug, P.
    Martic, T. Nikuseva
    Maksimovic, B.
    Simunov, B.
    Ljubanovic, D. Galesic
    VIRCHOWS ARCHIV, 2021, 479 : S273 - S273
  • [46] Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome
    Shaw, Elizabeth A.
    Colville, Deb
    Wang, Yan Yan
    Zhang, Ke Wei
    Dagher, Hayat
    Fassett, Rob
    Guymer, Robyn
    Savige, Judy
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2007, 22 (01) : 104 - 108
  • [47] Gene expression analysis in a canine model of X-linked Alport syndrome
    Greer, Kimberly A.
    Higgins, Marnie A.
    Cox, Melissa L.
    Ryan, Timothy P.
    Berridge, Brian R.
    Kashtan, Clifford E.
    Lees, George E.
    Murphy, Keith E.
    MAMMALIAN GENOME, 2006, 17 (09) : 976 - 990
  • [48] Glomerular expression of type TV collagen in X-linked Alport syndrome
    Heidet, L
    Cai, Y
    Guicharnaud, L
    Antignac, C
    Gubler, MC
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 113 (06) : 1145 - 1145
  • [49] Genetic cause of X-linked Alport syndrome in a family of domestic dogs
    Cox, ML
    Lees, GE
    Kashtan, CE
    Murphy, KE
    MAMMALIAN GENOME, 2003, 14 (06) : 396 - 403
  • [50] Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome
    Colville, DJ
    Shaw, A
    Wang, Y
    Dagher, H
    Fassett, R
    Savige, J
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2005, 46