Davarmanesh Mehdy, Zahed Maryam, Sookhakian Asma, Jehbez Sina
Department of Oral and Maxillofacial Medicine, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran.
Oral and Dental Disease Research Center, Department of Oral and Maxillofacial Medicine, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran.
Evid Based Complement Alternat Med. 2022 Sep 17;2022:7583691. doi: 10.1155/2022/7583691. eCollection 2022.
Treating oral mucosal lesions of Pemphigus Vulgaris (PV) disease is usually challenging for clinicians. We studied the treatment outcomes of the oral PV patients referred to the Oral Medicine Department of Shiraz University of Medical Sciences from 2004 to 2018.
The medical records of 54 oral PV patients with histopathological confirmation who were treated by a single protocol were studied. The protocol consisted of initial treatment with 1 mg/kg/day of oral prednisolone for all patients. After 4-6 weeks, all patients were prescribed 40 mg of prednisolone. If lesion recovery was not observed or new lesions had developed, adjuvant therapy (maximum dose of 200 mg per day of Azathioprine (AZA)) was initiated anytime during the treatment. The oral prednisolone dosage was gradually tapered to 5 mg/alternate day in 9 months.
47 patients were included in the study. 34.04% were male and 65.96% were female with a mean age of 41.83 ± 12.520. The mean follow-up period was 50.806 ± 44.417 months (over 4 years). The severity of oral involvement was mild in 21.27%, moderate in 36.17%, and severe in 42.6%. During treatment, all patients except one experienced complete remission. The mean time to achieve complete remission was 150.39 ± 224.075 days. Most of the patients experienced relapse due to self-discontinuation of treatment. 55% had complete remission and 43% were in partial remission at the last follow-up session. In 65.96% of patients, treatment-associated side effects were observed. The patients treated with prednisolone alone had significantly more side effects than those using AZA as an adjuvant (80% vs 50%, respectively; =0.030). The mean duration of follow-ups was longer for patients with side effects ( < 0.01). Topical corticosteroids were used for all patients sometime during the treatment. No deaths were recorded.
Prescribing low-dose prednisolone and adding AZA in nonresponding cases has good clinical outcomes for the treatment of oral lesions of PV. Adjuvant therapy can avoid the increase in corticosteroid dosage and side effects. The treatment method described in this study can be a helpful guide for clinicians, especially when other immunosuppressive drugs are not available.
治疗寻常型天疱疮(PV)的口腔黏膜病变对临床医生来说通常具有挑战性。我们研究了2004年至2018年转诊至设拉子医科大学口腔医学系的口腔PV患者的治疗结果。
研究了54例经组织病理学确诊且采用单一方案治疗的口腔PV患者的病历。该方案包括所有患者初始口服泼尼松龙,剂量为1mg/kg/天。4-6周后,所有患者均服用40mg泼尼松龙。如果未观察到病变恢复或出现新病变,则在治疗期间的任何时间开始辅助治疗(硫唑嘌呤(AZA)最大剂量为每天200mg)。口服泼尼松龙剂量在9个月内逐渐减至5mg/隔日。
47例患者纳入研究。男性占34.04%,女性占65.96%,平均年龄为41.83±12.520岁。平均随访期为50.806±44.417个月(超过4年)。口腔受累严重程度轻度占21.27%,中度占36.17%,重度占42.6%。治疗期间,除1例患者外,所有患者均实现完全缓解。实现完全缓解的平均时间为150.39±224.075天。大多数患者因自行停药而复发。在最后一次随访时,55%的患者完全缓解,43%的患者部分缓解。65.96%的患者观察到治疗相关副作用。单独使用泼尼松龙治疗的患者比使用AZA作为辅助治疗的患者副作用明显更多(分别为80%和50%;P=0.030)。有副作用的患者平均随访时间更长(P<0.01)。所有患者在治疗期间的某个时间都使用了局部皮质类固醇。无死亡记录。
开具低剂量泼尼松龙并在无反应病例中添加AZA对治疗PV的口腔病变具有良好的临床效果。辅助治疗可避免皮质类固醇剂量增加和副作用。本研究中描述的治疗方法可为临床医生提供有益指导,尤其是在没有其他免疫抑制药物的情况下。