Barnadas Maria A, Curell Román, Alomar Agustín, Gelpí Carmen
Department of Dermatology, Hospital Sta. Creu i St. Pau, Barcelona, Spain.
J Cutan Pathol. 2009 Jan;36(1):34-8. doi: 10.1111/j.1600-0560.2008.00993.x. Epub 2008 Jun 17.
Paraneoplastic pemphigus (PNP) is considered an autoimmune, multiorgan disease caused by antiplakin antibodies. We present three PNP patients who had negative epithelial direct immunofluorescence (DIF) findings in one or more biopsies.
An early lip biopsy of uninvolved oral epithelia in patient 1 was negative. A later biopsy from foreskin showed intense intercellular immunoglobulin G (IgG) deposits in the epithelia. In the early phase of the disease in patient 2, the intercellular fluorescence was negative in the epidermis, while intercellular IgG and C3 were observed in the sweat ducts. A later biopsy showed weak intercellular epidermal IgG and C3 fluorescence. Patient 3 showed intercellular IgG and/or C3 in follicular, sebaceous and sweat duct structures in several biopsies. No intercellular IgG or C3 was observed in the epithelia.
The presence of immunoreactants in adnexal structures suggests that desmoplakins can be more strongly expressed in adnexa than in the epidermis, facilitating visualization of antibody deposits.
Negative DIF findings in epithelia do not rule out the diagnosis of PNP, and the presence of IgG and/or C3 at the intercellular level of adnexal structures can help establish this diagnosis.
副肿瘤性天疱疮(PNP)被认为是一种由抗桥粒斑蛋白抗体引起的自身免疫性多器官疾病。我们报告了3例PNP患者,他们在一次或多次活检中上皮直接免疫荧光(DIF)检查结果为阴性。
患者1未受累口腔上皮的早期唇部活检结果为阴性。后来取自包皮的活检显示上皮细胞间有强烈的免疫球蛋白G(IgG)沉积。患者2在疾病早期,表皮细胞间荧光为阴性,而在汗腺导管中观察到细胞间IgG和C3。后来的活检显示表皮细胞间IgG和C3荧光较弱。患者3在多次活检中,在毛囊、皮脂腺和汗腺导管结构中显示细胞间IgG和/或C3。在上皮细胞中未观察到细胞间IgG或C3。
附属器结构中存在免疫反应物表明桥粒斑蛋白在附属器中的表达可能比在表皮中更强,这有利于抗体沉积的显现。
上皮DIF检查结果为阴性不能排除PNP的诊断,附属器结构细胞间水平存在IgG和/或C3有助于确立这一诊断。