Efficacy of alprostadil in chilblain lupus erythematosus

IF 2.3 4区 医学 Q2 DERMATOLOGY
Wei-En Wang, Chung-Hsing Chang
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(f and g) Bilateral hand magnetic resonance angiography showed patent distal radial arteries, ulnar to interdigital arteries, and postcontrast enhancement of soft tissue swelling over the 1st to 5th digits.Blood tests revealed high titers of anti-Ro/SSA antibodies (50.1 EliA U/mL) and low C4 levels (18.2 mg/dL). However, she tested negative for antinuclear antibodies (ANA), anticardiolipin antibodies, anti-Scl-70 antibodies, and anti-double-stranded DNA antibodies. The cryoglobulin and cold agglutinin tests were negative. A diagnosis of systemic lupus erythematosus (SLE) was not fulfilled. Bilateral hand magnetic resonance angiography showed patent distal radial arteries, ulnar to interdigital arteries, and postcontrast enhancement of soft-tissue swelling over the 1st to 5th digits [Figure 1f and g]. Based on her clinical symptoms and laboratory results, she was diagnosed with chilblain lupus erythematosus (CHLE). The proposed CHLE diagnostic criteria have not yet been validated, although the Mayo Clinic diagnostic criteria proposed by Su et al. include clinical presentation, laboratory findings, and histopathology.[1] She was treated with oral pentoxifylline and nifedipine for 5 months; however, only mild improvement was seen. We further administrated a 10-day regimen of intravenous alprostadil at a dose of 60 µg/day. Significant improvement in the digital ulcers was observed within 2 weeks [Figure 2a]. Laser Doppler flowmetry revealed increased microvascular perfusion in the digits of the left hand at 30°C and 44°C during the 8-week follow-up [Figure 2b].Figure 2: (a) The digital ulcers showed significant improvement within 2 weeks (left hand). (b) Laser Doppler flowmetry revealed an increase in microvascular perfusion in the middle digit of the left hand both at 30°C and 44°C after alprostadil treatment during an 8-week follow-up.CHLE is a rare form of cutaneous lupus erythematosus; based on previous studies, it coexists with SLE in 33%–88% of patients.[2,3] Moreover, SLE developed in these patients before or after the onset of CHLE.[2,3] CHLE lesions initially present as violaceous-erythematous papules and plaques on the toes, fingers, or face, and they worsen during exposure to cold stimuli or decreased temperature. As CHLE lesions progress, hyperkeratosis, ulceration, and dyspigmentation may occur. The antibody profile of CHLE is nonspecific.[4] Among patients with CHLE, 80% were ANA positive and 50% were anti-SSA positive, according to a retrospective study involving 30 patients.[3] The treatment for CHLE has not been standardized, although the protection from the cold is an integral part of its management. The current treatment options consist of topical or systemic corticosteroids, topical calcineurin inhibitors, antimalarials, or immunomodulators, such as mycophenolate mofetil, depending on the severity of the disease. Furthermore, calcium channel blockers are reportedly beneficial against vasoconstriction.[5] Prostaglandin E1, also known as alprostadil, has been used to treat peripheral circulatory insufficiency as it induces vasodilation and angiogenesis and inhibits platelet aggregation, leukocyte adhesion, and inflammation.[6,7] In the current study, alprostadil was the first used to treat digital ulcers in a patient with CHLE. Alprostadil (30 μg) was dissolved in 0.9% normal saline (500 mL) and administered intravenously over a 2-h period, twice daily for 10 days. Significant improvement in pain and ulceration was observed within 2 weeks. Laser Doppler flowmetry demonstrated increased microvascular perfusion of the digits during the 8-week follow-up period. Few studies have discussed CHLE, and this case report highlighted the efficacy of alprostadil in the treatment of CHLE. Further investigation and long-term follow-up will be conducted. Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given her consent for her images and other clinical information to be reported in the journal. The patient understands that name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed. Data availability statement The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request. Financial support and sponsorship Nil. Conflicts of interest Prof. Chung-Hsing Chang, an editorial board member at Dermatologica Sinica, had no role in the peer review process of or decision to publish this article. 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引用次数: 0

Abstract

Dear Editor, A 56-year-old woman presented with chronic pain in her digits. She had worked in the seafood frozen-packaging line of a food factory for many years. Physical examination revealed ulcerations on the pulps and knuckles of her digits, with hyperkeratosis and fissures [Figure 1a-d]. No similar lesions on toes were found. The lesions were worsened by exposure to a cold environment. Raynaud’s phenomenon and sclerodactyly were not observed. In addition, a patch of cicatricial alopecia was observed on the vertex of the scalp [Figure 1e]. Discoid lupus erythematosus was confirmed by skin biopsy.Figure 1: (a-d) Erythematous plaques with fissures and ulceration on the fingers and pulps of the digits. (e) A patch of cicatricial alopecia on the vertex of the scalp. (f and g) Bilateral hand magnetic resonance angiography showed patent distal radial arteries, ulnar to interdigital arteries, and postcontrast enhancement of soft tissue swelling over the 1st to 5th digits.Blood tests revealed high titers of anti-Ro/SSA antibodies (50.1 EliA U/mL) and low C4 levels (18.2 mg/dL). However, she tested negative for antinuclear antibodies (ANA), anticardiolipin antibodies, anti-Scl-70 antibodies, and anti-double-stranded DNA antibodies. The cryoglobulin and cold agglutinin tests were negative. A diagnosis of systemic lupus erythematosus (SLE) was not fulfilled. Bilateral hand magnetic resonance angiography showed patent distal radial arteries, ulnar to interdigital arteries, and postcontrast enhancement of soft-tissue swelling over the 1st to 5th digits [Figure 1f and g]. Based on her clinical symptoms and laboratory results, she was diagnosed with chilblain lupus erythematosus (CHLE). The proposed CHLE diagnostic criteria have not yet been validated, although the Mayo Clinic diagnostic criteria proposed by Su et al. include clinical presentation, laboratory findings, and histopathology.[1] She was treated with oral pentoxifylline and nifedipine for 5 months; however, only mild improvement was seen. We further administrated a 10-day regimen of intravenous alprostadil at a dose of 60 µg/day. Significant improvement in the digital ulcers was observed within 2 weeks [Figure 2a]. Laser Doppler flowmetry revealed increased microvascular perfusion in the digits of the left hand at 30°C and 44°C during the 8-week follow-up [Figure 2b].Figure 2: (a) The digital ulcers showed significant improvement within 2 weeks (left hand). (b) Laser Doppler flowmetry revealed an increase in microvascular perfusion in the middle digit of the left hand both at 30°C and 44°C after alprostadil treatment during an 8-week follow-up.CHLE is a rare form of cutaneous lupus erythematosus; based on previous studies, it coexists with SLE in 33%–88% of patients.[2,3] Moreover, SLE developed in these patients before or after the onset of CHLE.[2,3] CHLE lesions initially present as violaceous-erythematous papules and plaques on the toes, fingers, or face, and they worsen during exposure to cold stimuli or decreased temperature. As CHLE lesions progress, hyperkeratosis, ulceration, and dyspigmentation may occur. The antibody profile of CHLE is nonspecific.[4] Among patients with CHLE, 80% were ANA positive and 50% were anti-SSA positive, according to a retrospective study involving 30 patients.[3] The treatment for CHLE has not been standardized, although the protection from the cold is an integral part of its management. The current treatment options consist of topical or systemic corticosteroids, topical calcineurin inhibitors, antimalarials, or immunomodulators, such as mycophenolate mofetil, depending on the severity of the disease. Furthermore, calcium channel blockers are reportedly beneficial against vasoconstriction.[5] Prostaglandin E1, also known as alprostadil, has been used to treat peripheral circulatory insufficiency as it induces vasodilation and angiogenesis and inhibits platelet aggregation, leukocyte adhesion, and inflammation.[6,7] In the current study, alprostadil was the first used to treat digital ulcers in a patient with CHLE. Alprostadil (30 μg) was dissolved in 0.9% normal saline (500 mL) and administered intravenously over a 2-h period, twice daily for 10 days. Significant improvement in pain and ulceration was observed within 2 weeks. Laser Doppler flowmetry demonstrated increased microvascular perfusion of the digits during the 8-week follow-up period. Few studies have discussed CHLE, and this case report highlighted the efficacy of alprostadil in the treatment of CHLE. Further investigation and long-term follow-up will be conducted. Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given her consent for her images and other clinical information to be reported in the journal. The patient understands that name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed. Data availability statement The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request. Financial support and sponsorship Nil. Conflicts of interest Prof. Chung-Hsing Chang, an editorial board member at Dermatologica Sinica, had no role in the peer review process of or decision to publish this article. The other authors declared no conflicts of interest in writing this paper.
前列地尔治疗冻疮红斑狼疮疗效观察
亲爱的编辑:一位56岁的女性,因手指慢性疼痛而就诊。她曾在一家食品厂的海鲜冷冻包装生产线工作多年。体格检查显示其指髓和指关节溃疡,角化过度和裂缝[图1a-d]。足趾未见类似病变。暴露在寒冷的环境中会使病变恶化。未观察到雷诺现象和指关节硬化。此外,在头皮顶点处观察到一块瘢痕性脱发[图1e]。皮肤活检证实为盘状红斑狼疮。图1:(a-d)手指和指髓的红斑斑块伴裂隙和溃疡。(e)头皮顶点的一块瘢痕性脱发。(f和g)双侧手磁共振血管造影显示桡动脉远端通畅,尺侧至指间动脉通畅,1 - 5趾软组织肿胀增强。血液检查显示抗ro /SSA抗体高滴度(50.1 EliA U/mL)和低C4水平(18.2 mg/dL)。然而,她的抗核抗体(ANA)、抗心磷脂抗体、抗scl -70抗体和抗双链DNA抗体检测均为阴性。冷球蛋白和冷凝集素试验均为阴性。诊断为系统性红斑狼疮(SLE)不满足。双侧手磁共振血管造影显示桡动脉远端通畅,尺侧至指间动脉通畅,1 - 5趾软组织肿胀增强[图1f和g]。根据她的临床症状和实验室结果,诊断为冻疮红斑狼疮(CHLE)。虽然Su等人提出的梅奥诊所诊断标准包括临床表现、实验室结果和组织病理学,但建议的CHLE诊断标准尚未得到验证。[1]口服己酮茶碱、硝苯地平5个月;然而,只看到了轻微的改善。我们进一步以60µg/天的剂量静脉注射前列地尔,为期10天。2周内观察到手指溃疡的显著改善[图2a]。激光多普勒血流仪显示,在8周的随访中,在30°C和44°C时,左手手指微血管灌注增加[图2b]。图2:(a)手指溃疡在2周内明显改善(左手)。(b)激光多普勒血流测量显示,在8周的随访中,前列地尔治疗后,左手中指在30°C和44°C时微血管灌注增加。CHLE是一种罕见的皮肤红斑狼疮;根据以往的研究,33%-88%的患者与SLE共存。[2,3]此外,这些患者在CHLE发病之前或之后发生SLE。[2,3] CHLE病变最初表现为脚趾、手指或面部的紫色红斑丘疹和斑块,并在暴露于寒冷刺激或温度降低时恶化。随着CHLE病变的进展,可能会出现角化过度、溃疡和色素沉着。CHLE的抗体谱是非特异性的[4]。一项涉及30例CHLE患者的回顾性研究显示,80%的CHLE患者ANA阳性,50%的CHLE患者抗ssa阳性[3]。CHLE的治疗尚未标准化,尽管防寒是其管理的一个组成部分。目前的治疗方案包括局部或全身皮质类固醇、局部钙调磷酸酶抑制剂、抗疟药或免疫调节剂,如霉酚酸酯,这取决于疾病的严重程度。此外,据报道,钙通道阻滞剂对血管收缩有益。[5]前列腺素E1,又称前列地尔,已被用于治疗外周循环功能不全,因为它能诱导血管舒张和血管生成,抑制血小板聚集、白细胞粘附和炎症。[6,7]在目前的研究中,前列地尔是第一个用于治疗CHLE患者手指溃疡的药物。将前列地尔(30 μg)溶于0.9%生理盐水(500 mL)中,静脉滴注2 h,每日2次,连用10 d。2周内疼痛和溃疡明显改善。激光多普勒血流测量显示,在8周的随访期间,手指微血管灌注增加。很少有研究讨论CHLE,本病例报告强调了前列地尔治疗CHLE的疗效。将进行进一步调查和长期随访。患者同意声明作者证明他们已经获得了所有适当的患者同意表格。在此表格中,患者已同意她的图像和其他临床信息将在杂志上报道。患者明白姓名和首字母不会被公布,并将尽力隐藏身份,但不能保证匿名。
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来源期刊
Dermatologica Sinica
Dermatologica Sinica DERMATOLOGY-
CiteScore
2.80
自引率
20.00%
发文量
28
审稿时长
>12 weeks
期刊介绍: Dermatologica Sinica aims to publish high quality scientific research in the field of dermatology, with the goal of promoting and disseminating dermatological-related medical science knowledge to improve global health. Articles on clinical, laboratory, educational, and social research in dermatology and other related fields that are of interest to the medical profession are eligible for consideration. Review articles, original articles, brief reports, case reports and correspondence are accepted.
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