Non-paraneoplastic autoimmune subepidermal bullous disease associated with fatal bronchiolitis obliterans

被引:3
作者
Orime, Mari [1 ]
Tomiyama, Katsuhiro [2 ]
Hashidate, Hideki [3 ]
Yoshida, Satoru [4 ]
Hokari, Satoshi [5 ]
Tsuda, Akiko [6 ]
Yokoyama, Hisashi [7 ]
Narita, Jun-ichi [8 ]
Uchida, Youhei [9 ]
Kanekura, Takuro [9 ]
Abe, Riichiro [1 ]
Ishii, Norito [10 ,11 ]
Hashimoto, Takashi [10 ,11 ]
Kawai, Kazuhiro [9 ,12 ]
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Div Dermatol, Niigata, Japan
[2] Niigata City Gen Hosp, Dept Dermatol, Niigata, Japan
[3] Niigata City Gen Hosp, Dept Pathol, Niigata, Japan
[4] Niigata City Gen Hosp, Dept Emergency & Crit Care Med Ctr, Niigata, Japan
[5] Niigata Univ, Grad Sch Med & Dent Sci, Dept Resp Med & Infect Dis, Niigata, Japan
[6] Kido Hosp, Dept Endocrinol & Metab, Niigata, Japan
[7] Kido Hosp, Dept Gastroenterol & Hepatol, Niigata, Japan
[8] Kido Hosp, Dept Resp Med, Niigata, Japan
[9] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Dermatol, Kagoshima, Japan
[10] Kurume Univ, Sch Med, Dept Dermatol, Kurume, Fukuoka, Japan
[11] Kurume Univ, Inst Cutaneous Cell Biol, Kurume, Fukuoka, Japan
[12] Kido Hosp, Dept Dermatol, Niigata, Japan
基金
日本学术振兴会;
关键词
bronchiolitis obliterans; collagen type XVII; kalinin; linear immunoglobulin A bullous dermatosis; pemphigoid; PEMPHIGUS; IGA; DERMATOSIS; ANTIBODIES; ANTIGENS; CELLS;
D O I
10.1111/1346-8138.13706
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Bronchiolitis obliterans is a small-airway obstructive lung disease for which immunologically mediated pathogenesis is supposed. Frequent association of bronchiolitis obliterans with paraneoplastic pemphigus is well known, but its association with other autoimmune bullous diseases has not been reported except for a case of anti-laminin-332-type mucous membrane pemphigoid in a patient with chronic graft-versus-host disease. We report a case of non-paraneoplastic autoimmune subepidermal bullous disease associated with fatal bronchiolitis obliterans in a patient without transplantation. Although the patient's serum contained immunoglobulin (Ig)A antibodies to the 180-kDa bullous pemphigoid antigen/type XVII collagen and IgG antibodies to laminin-332, diagnosis of either linear IgA bullous dermatosis or mucous membrane pemphigoid could not be made because of the failure to detect linear IgA deposition at the basement membrane zone by direct immunofluorescence and the lack of mucous membrane lesions. Physicians should be aware that autoimmune bullous diseases other than paraneoplastic pemphigus can also associate with this rare but potentially fatal lung disease.
引用
收藏
页码:461 / 464
页数:4
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