Esophagogastroduodenoscopy and Esophageal Involvement in Patients with Pemphigus Vulgaris

被引:0
作者
Katharine A. Ozeki
Thomas A. Zikos
John O. Clarke
Irene Sonu
机构
[1] Stanford University School of Medicine,Department of Medicine
[2] Stanford University School of Medicine,Division of Gastroenterology and Hepatology, Department of Medicine
来源
Dysphagia | 2020年 / 35卷
关键词
Esophagogastroduodenoscopy; Autoimmune; Pemphigus vulgaris; Dysphagia; Esophageal symptoms; Deglutition; Deglutition disorders;
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摘要
Pemphigus vulgaris (PV) is a rare autoimmune blistering disease involving the skin and mucous membranes. The prevalence of esophageal involvement remains uncertain. The aim of our study was to determine the frequency of esophageal involvement in patients with PV. This is a single-center electronic database retrospective review of patients with a diagnosis of PV. Data abstracted included demographics, disease characteristics (biopsy results, symptoms, areas affected, treatments), and esophagogastroduodenoscopy (EGD) reports. Of the 111 patients that met eligibility criteria, only 22 (19.8%) underwent EGD. Demographic data were similar except those who underwent EGD were more likely to be female (77.3% vs. 51.7%, p = 0.05) and have hypertension (50.0% vs. 24.7%, p = 0.04). Esophageal symptoms were common in both groups; however, those experiencing dysphagia were more likely to undergo EGD (50.0% vs. 20.2%, p = 0.007). Those who underwent EGD had more refractory disease (≥ 3 treatment modalities: 100% vs. 58.4%, p < 0.001), but did not differ in areas affected. Of those who underwent EGD, only 4 (18.2%) had esophageal abnormalities either prior to PV diagnosis (1) or during a disease flare (3). Those having a flare were more likely to experience odynophagia (69.2%) or weight loss (61.5%), p = 0.02 and p = 0.05, respectively. While esophageal symptoms were common in our cohort of PV patients, a minority of patients underwent EGD, and the vast majority of those were unremarkable. This suggests that while esophageal symptoms are common in PV, permanent esophageal injury is more rare.
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页码:503 / 508
页数:5
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[1]  
Mihai S(2007)Immunopathology and molecular diagnosis of autoimmune bullous diseases J Cell Mol Med 11 462-481
[2]  
Sitaru C(1996)Pemphigus: from immunofluorescence to molecular biology J Dermatol Sci 12 1-9
[3]  
Nishikawa T(2005)Pemphigus Lancet 366 61-73
[4]  
Hashimoto T(2015)Oral mucosal manifestations of autoimmune skin diseases Autoimmun Rev 14 930-951
[5]  
Shimizu H(2011)Ear, nose and throat involvement in patients with pemphigus vulgaris: correlation with severity, phenotype and disease activity J Eur Acad Dermatol Venereol 25 1324-1327
[6]  
Ebihara T(2015)Genital involvement in pemphigus vulgaris (PV): correlation with clinical and cervicovaginal Pap smear findings J Am Acad Dermatol 73 655-659
[7]  
Amagai M(1996)The adjuvant therapy of pemphigus. An update Arch Dermatol 132 203-212
[8]  
Bystryn JC(2009)Mortality of bullous skin disorders from 1979 through 2002 in the United States Arch Dermatol 145 1005-1008
[9]  
Rudolph JL(2008)Bullous pemphigoid and pemphigus vulgaris–incidence and mortality in the UK: population based cohort study BMJ 337 a180-199
[10]  
Mustafa MB(2005)The role of upper endoscopy in identifying oesophageal involvement in patients with oral pemphigus vulgaris Dig Liver Dis 37 195-519