Chorzelski T, Hashimoto T, Maciejewska B, Amagai M, Anhalt G J, Jablonska S
Department of Dermatology, Warsaw School of Medicine, Poland.
J Am Acad Dermatol. 1999 Sep;41(3 Pt 1):393-400. doi: 10.1016/s0190-9622(99)70111-8.
Cases of paraneoplastic pemphigus (PNP) have been reported associated with various lymphoproliferative malignancies and benign Castleman tumors, with the most severe course and fatal outcome seen in patients with bronchiolitis obliterans.
The aim was to establish immunologic associations by coexistence of Castleman tumor, myasthenia gravis, and bronchiolitis obliterans and to evaluate the treatment modalities.
Clinical studies included computed tomography of the mediastinum, computed tomography and magnetic resonance imaging of the abdominal cavity, and quantitative electromyography. Direct and indirect immunofluorescence on various substrates, immunoblot analysis, immunoprecipitation, and specific enzyme-linked immunosorbent assay using recombinant desmogleins (Dsg) were performed as immunologic assays.
Direct and indirect immunofluorescence including rat bladder showed intercellular antibodies. Immunoblotting disclosed antibodies to envoplakin (210 kd protein) and periplakin (190 kd protein); in addition, immunoprecipitation detected antibodies to desmoplakin I (250 kd protein). Antibodies to Dsg3 (pemphigus vulgaris antigen) were detected by specific enzyme-linked immunosorbent assay. Myasthenia gravis was controlled by drugs; however, mucocutaneous changes were not fully responsive to corticosteroids and cyclophosphamide pulses, cyclosporine, and intravenous immunoglobulins. The surgical removal of Castleman tumor did not change the course of the disease. The fatal outcome was the result of bronchiolitis obliterans that occurred after the surgery and was only transitionally controlled by plasmapheresis.
This is the first case of paraneoplastic pemphigus associated with Castleman tumor, myasthenia gravis, and bronchiolitis obliterans. Despite a benign character of the tumor the patient died, as do all patients with bronchiolitis obliterans. Massive plasmapheresis has only a transient effect. We confirmed the presence of antibodies to Dsg 3, in addition to the set of specific paraneoplastic pemphigus antibodies against various proteins of plakin family.
副肿瘤性天疱疮(PNP)病例已被报道与各种淋巴增生性恶性肿瘤和良性Castleman肿瘤相关,闭塞性细支气管炎患者的病程最为严重且预后 fatal。
通过Castleman肿瘤、重症肌无力和闭塞性细支气管炎共存来建立免疫关联,并评估治疗方式。
临床研究包括纵隔计算机断层扫描、腹腔计算机断层扫描和磁共振成像以及定量肌电图。作为免疫测定,对各种底物进行直接和间接免疫荧光、免疫印迹分析、免疫沉淀以及使用重组桥粒芯糖蛋白(Dsg)的特异性酶联免疫吸附测定。
包括大鼠膀胱在内的直接和间接免疫荧光显示细胞间抗体。免疫印迹揭示了针对内披蛋白(210kd蛋白)和周膜蛋白(190kd蛋白)的抗体;此外,免疫沉淀检测到针对桥粒斑蛋白I(250kd蛋白)的抗体。通过特异性酶联免疫吸附测定检测到针对Dsg3(寻常型天疱疮抗原)的抗体。重症肌无力通过药物得到控制;然而,皮肤黏膜改变对皮质类固醇、环磷酰胺脉冲、环孢素和静脉注射免疫球蛋白反应不完全。Castleman肿瘤的手术切除并未改变疾病进程。fatal结局是手术后发生的闭塞性细支气管炎的结果,并仅通过血浆置换得到短暂控制。
这是首例与Castleman肿瘤、重症肌无力和闭塞性细支气管炎相关的副肿瘤性天疱疮病例。尽管肿瘤具有良性特征,但患者仍死亡,闭塞性细支气管炎患者均如此。大规模血浆置换仅具有短暂效果。除了一组针对桥粒斑蛋白家族各种蛋白质的特异性副肿瘤性天疱疮抗体外我们还证实了针对Dsg 3抗体的存在。