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A Case of Allopurinol-Induced Drug Reaction with Eosinophilia and Systemic Symptoms in a Patient With Polycystic Kidney Disease and Chronic Kidney Disease. 别嘌呤醇诱导的药物反应伴嗜酸性粒细胞增多及慢性肾病患者全身症状1例
Emily Koller, Neil Dixit, Remy Lee, Pinky Jha

Introduction: Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a severe drug hypersensitivity reaction.

Case presentation: A 59-year-old male with a history of stage IV chronic kidney disease, polycystic kidney disease, hypertension, and hyperuricemia on allopurinol presented to the emergency department directly from an outpatient nephrology appointment with concern for severe DRESS syndrome with acute-on-chronic kidney failure, liver failure, and pancreatic involvement.

Discussion: The existing literature on the course of DRESS syndrome in patients with preexisting kidney dysfunction is limited.

Conclusions: We report a case of DRESS syndrome in a patient with chronic kidney disease who presented after initiating allopurinol for hyperuricemia. Care should be taken to quickly identify DRESS, stop the offending agent, and initiate systemic corticosteroids to prevent long-term morbidity and mortality. Furthermore, patient counseling should emphasize follow-up to identify and treat potential long-term sequelae, including thyroiditis and cardiac disease.

药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)综合征是一种严重的药物超敏反应。病例介绍:一名59岁男性,有IV期慢性肾病、多囊肾病、高血压和别嘌呤醇所致的高尿酸血症病史,因严重DRESS综合征并发急性慢性肾衰竭、肝功能衰竭和胰腺受累,直接从门诊肾脏病预约就诊到急诊科。讨论:关于既往肾功能不全患者DRESS综合征病程的现有文献有限。结论:我们报告了一例慢性肾病患者在服用别嘌呤醇治疗高尿酸血症后出现DRESS综合征。应注意迅速识别DRESS,停用不良药物,并开始全身性皮质类固醇治疗,以防止长期发病率和死亡率。此外,患者咨询应强调随访,以识别和治疗潜在的长期后遗症,包括甲状腺炎和心脏病。
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引用次数: 0
Epidemiology of Xylazine-Positive Fatal Overdoses in Milwaukee County, Wisconsin, 2019-2023. 2019-2023年威斯康星州密尔沃基县噻嗪阳性致死性用药过量流行病学
Max Mantych, Cassandra Laibly, Hunter Russell, Kirsten M M Beyer, Yuhong Zhou, Ronald Anguzu

Introduction: Xylazine association with fentanyl poses an emerging threat to public health. We conducted a retrospective study to analyze xylazine-related fatal overdoses in Milwaukee County, Wisconsin from 2019 through 2023.

Methods: Using medical examiner data, we compared fatal xylazine overdoses (n = 243) with fentanyl overdoses without xylazine (n = 1946). Demographic, polysubstance, temporal, and geographic characteristics were analyzed.

Results: Xylazine fatalities have surged since 2019, exhibiting different polysubstance profiles than fentanyl overdoses without xylazine. We identified 8 geospatial clusters contributing to 64% of xylazine overdoses.

Discussion: We encourage localized interventions to address the xylazine-fentanyl syndemic. Policy measures such as Wisconsin Act 217, which legalized xylazine testing materials, promote evidence-based harm reduction tools to mitigate the risks associated with xylazine's increasing prevalence in the Midwest.

简介:噻嗪与芬太尼的联用对公众健康构成了新的威胁。我们进行了一项回顾性研究,分析了2019年至2023年威斯康星州密尔沃基县与氯嗪相关的致命过量用药。方法:利用法医资料,将致死性过量使用噻嗪(n = 243)与未使用噻嗪的芬太尼过量使用(n = 1946)进行比较。分析了人口统计学、多物质、时间和地理特征。结果:自2019年以来,噻嗪类药物死亡人数激增,与不含噻嗪的芬太尼类药物过量相比,表现出不同的多物质特征。我们确定了8个地理空间集群导致64%的噻嗪过量。讨论:我们鼓励采取局部干预措施来解决噻嗪-芬太尼综合症。政策措施,如威斯康星州第217号法案,该法案将木嗪检测材料合法化,促进了以证据为基础的减少危害工具,以减轻木嗪在中西部日益流行的风险。
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引用次数: 0
Proceedings from the 2024 Medical College of Wisconsin Innovations in Healthcare Education Research Annual Conference. 2024年威斯康星医学院医疗保健教育创新研究年会论文集。
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引用次数: 0
Assessing the Educational Needs of Wisconsin Primary Care Clinicians Caring for Persons Living With Dementia. 评估威斯康星州初级保健临床医生照顾痴呆症患者的教育需求。
Tyler Ballweg, Tamara J LeCaire, Uriel Paniagua, Molly Schroeder, Tammi Albrecht, Sarina Schrager, Cynthia M Carlsson, Art Walaszek

Introduction: Nearly 90% of persons living with dementia experience behavioral and psychological symptoms of dementia (BPSD). Primary care clinicians may require more training to address these symptoms.

Methods: We surveyed Wisconsin primary care clinicians to assess their current approaches, needs, and interest in future educational interventions related to managing BPSD.

Results: Over 60% of clinicians reported lack of ability or training in managing BPSD, while over 75% expressed interest in educational interventions that included discussion of treatment algorithms or virtual didactics.

Discussion: Given the apparent widespread demand and need for educational interventions on BPSD for primary care clinicians, future studies are needed to assess the efficacy of such interventions in improving clinicians' preparedness to care for patients with BPSD.

引言:我们调查了威斯康星州的初级保健临床医生,以评估他们目前的方法、需求和对未来与管理BPSD相关的教育干预的兴趣。方法:利用法医资料,将致死性过量使用噻嗪(n = 243)与未使用噻嗪的芬太尼过量使用(n = 1946)进行比较。分析了人口统计学、多物质、时间和地理特征。结果:超过60%的临床医生报告缺乏管理BPSD的能力或培训,而超过75%的临床医生表示对教育干预感兴趣,包括讨论治疗算法或虚拟教学。讨论:鉴于初级保健临床医生对BPSD的教育干预的明显广泛需求和需求,需要进一步的研究来评估这种干预在提高临床医生对BPSD患者护理准备方面的效果。
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引用次数: 0
Multiple Myeloma Presenting as Spinal Cord Compressive Plasmacytoma in Young Adults: A Case Series. 年轻人多发性骨髓瘤表现为脊髓压缩浆细胞瘤:一个病例系列。
Ryan T Shields, Nathan B Rose, Charlotte E Ball

Introduction: Multiple myeloma is a hematologic malignancy characterized by clonal proliferation of plasma cells. It is rare in young adults and may present in atypical forms, complicating timely diagnosis.

Case presentation: Patient 1 was a 23-year-old female who presented with subacute onset of leg pain, progressive weakness, and urinary retention. Lumbar spine magnetic resonance imaging (MRI) revealed a sacral mass causing cauda equina syndrome. Biopsy confirmed the diagnosis of plasmacytoma. At discharge, she exhibited gait abnormalities, neuropathic pain, and persistent urinary retention. She functioned at a modified independent level, using a manual wheelchair for mobility and performing intermittent self-catheterization. Patient 2 was a 28-year-old female who presented with acute onset of leg pain, weakness, and urinary retention. MRI of the spine revealed an epidural mass extending from T1 to T11, resulting in spinal cord compression. She underwent thoracolumbosacral laminectomies, and biopsy confirmed plasmacytoma. At discharge, she had motor complete paraplegia, neuropathic pain, and urinary retention managed with intermittent self-catheterization. She was modified independent, using a manual wheelchair for mobility.

Discussion: Despite advances in diagnosis and treatment, multiple myeloma remains a complex disease that poses diagnostic and therapeutic challenges. These cases emphasize the importance of standardized treatment protocols in management of spinal cord compressive plasmacytoma.

Conclusions: Early diagnosis, coordinated multidisciplinary care, and comprehensive rehabilitation are essential for improved management and outcomes.

简介:多发性骨髓瘤是一种以浆细胞克隆性增殖为特征的血液恶性肿瘤。它在年轻人中很少见,可能以非典型形式出现,使及时诊断复杂化。病例描述:患者1是一名23岁女性,表现为亚急性腿部疼痛,进行性虚弱和尿潴留。腰椎磁共振成像(MRI)显示一个骶骨肿块引起马尾综合征。活检证实浆细胞瘤的诊断。出院时,她表现出步态异常、神经性疼痛和持续性尿潴留。她在一个改良的独立水平上工作,使用手动轮椅行动,并进行间歇性的自我导尿。患者2是一名28岁女性,表现为急性腿部疼痛、虚弱和尿潴留。脊柱MRI显示硬膜外肿块从T1延伸至T11,导致脊髓受压。她接受了胸腰骶椎板切除术,活检证实为浆细胞瘤。出院时,患者出现运动性完全截瘫、神经性疼痛和尿潴留,并采用间歇性自我导尿。她被改造独立,使用手动轮椅行动。讨论:尽管在诊断和治疗方面取得了进展,多发性骨髓瘤仍然是一种复杂的疾病,给诊断和治疗带来了挑战。这些病例强调了标准化治疗方案在脊髓压缩浆细胞瘤管理中的重要性。结论:早期诊断、协调的多学科护理和全面康复对改善治疗和预后至关重要。
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引用次数: 0
Association of Frailty Score and Surgical Site Infection After Open Lower Extremity Revascularization. 开放性下肢血运重建术后虚弱评分与手术部位感染的关系。
Andrew Edsall, Andrew J Borgert, Alec Fitzsimmons, Irina Shakhnovich

Introduction: Surgical site infection (SSI) after lower extremity procedures is a persistent source of significant morbidity for vascular surgery patients. Frailty scores capture risk factors for postoperative outcomes associated with SSI. This study aimed to retrospectively evaluate the association between SSI and a validated measure of frailty, the Vascular Quality Initiative-Risk Analysis Index (VQI-RAI).

Methods: A retrospective review was performed of patients who underwent open lower extremity revascularization at a single independent academic medical center from January 1, 2007, through December 31, 2019. Frailty score was calculated using VQI-RAI, a composite score based on patient demographic and clinical variables. VQI-RAI scores were compared between patients who developed SSI and those who did not. SSI outcomes were compared between patients defined as frail (VQI-RAI ≥ 35) and not frail (VQI-RAI <  35).

Results: The study population comprised 1130 patients. The overall SSI rate was 8.1%. The median VQI-RAI score was 29 for patients with SSI and 28 for patients without SSI (P = 0.4). No significant association was observed between VQI-RAI and SSI or between patients defined as frail and not frail. Of the individual components of the VQI-RAI score, only body mass index was significantly associated with SSI (P <  .0001).

Conclusions: VQI-RAI frailty score was not associated with risk of SSI in our study population; however, body mass index was significantly associated with SSI. Obesity poses a high risk of SSI, whereas frailty alone may not be associated with an increased risk of SSI.

下肢手术后手术部位感染(SSI)是血管手术患者持续发病的重要原因。虚弱评分捕捉与SSI相关的术后结果的危险因素。本研究旨在回顾性评估SSI与虚弱的有效测量指标血管质量主动风险分析指数(VQI-RAI)之间的关系。方法:回顾性分析2007年1月1日至2019年12月31日在一家独立学术医疗中心接受开放性下肢血运重建术的患者。虚弱评分采用VQI-RAI计算,这是一种基于患者人口统计学和临床变量的综合评分。比较发生SSI和未发生SSI的患者的VQI-RAI评分。比较虚弱(VQI-RAI≥35)和非虚弱(VQI-RAI < 35)患者的SSI结果。结果:研究人群包括1130例患者。总体SSI率为8.1%。SSI患者的中位VQI-RAI评分为29分,无SSI患者的中位VQI-RAI评分为28分(P = 0.4)。VQI-RAI与SSI之间或虚弱与非虚弱患者之间未观察到显著关联。在VQI-RAI评分的各个组成部分中,只有体重指数与SSI显著相关(P < 0.0001)。结论:在我们的研究人群中,VQI-RAI衰弱评分与SSI风险无关;然而,体重指数与SSI显著相关。肥胖会增加SSI的风险,而虚弱本身可能与SSI风险增加无关。
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引用次数: 0
PAPASH Syndrome: A Case Report and Lessons for Clinical Practice. PAPASH综合征1例报告及临床经验。
Janvi Patel, Farzana Hoque

Introduction: PAPASH spectrum syndrome is a rare autoinflammatory condition encompassing psoriatic arthritis, pyoderma gangrenosum, acne, and hidradenitis suppurativa. Despite the individual prevalence of these conditions, their concurrent manifestation poses a diagnostic challenge that requires high clinical suspicion. This case illustrates the consequences of delayed recognition of this condition and underscores the crucial need for a multidisciplinary approach to optimize management.

Case presentation: We report the case of a 34-year-old African American man with a prior diagnosis of rheumatoid arthritis who developed migratory arthritis, pustular acne, and hidradenitis suppurativa. Despite suggestive clinical features, delayed access to biologic therapy contributed to disease progression and resulted in hospitalization. After extensive genetic and clinical evaluation, he was diagnosed with PAPASH syndrome.

Discussion: PAPASH syndrome is linked to mutations in the PSTPIP1 gene and the overexpression of specific chemokines, which dysregulate interleukin-1 signaling and cause persistent inflammation. Although tumor necrosis factor-α inhibitors remain first-line therapy, limited literature exists on comprehensive treatment strategies, and further research is needed. This case demonstrates how ongoing diagnostic ambiguity and the absence of clear treatment guidelines can complicate the management of PAPASH syndrome.

Conclusions: This case emphasizes the importance of prompt identification of PAPASH syndrome in patients presenting with overlapping inflammatory conditions and highlights the need for clinical vigilance, timely initiation of biologic agents, and coordinated care to improve outcomes in this rare but serious disorder.

简介:PAPASH谱系综合征是一种罕见的自身炎症性疾病,包括银屑病关节炎、坏疽性脓皮病、痤疮和化脓性汗腺炎。尽管这些情况的个体患病率,他们的并发表现提出了诊断的挑战,需要高度的临床怀疑。该病例说明了延迟认识这种情况的后果,并强调了对多学科方法优化管理的关键需要。病例介绍:我们报告一例34岁的非裔美国人,先前诊断为类风湿关节炎,后来发展为移动性关节炎、脓疱性痤疮和化脓性汗腺炎。尽管有提示的临床特征,但延迟获得生物治疗有助于疾病进展并导致住院。经过广泛的遗传和临床评估,他被诊断为PAPASH综合征。讨论:PAPASH综合征与PSTPIP1基因突变和特异性趋化因子的过度表达有关,这些趋化因子会失调白细胞介素-1信号传导并引起持续炎症。尽管肿瘤坏死因子-α抑制剂仍是一线治疗方法,但关于综合治疗策略的文献有限,需要进一步研究。该病例表明,持续的诊断模糊性和缺乏明确的治疗指南如何使PAPASH综合征的治疗复杂化。结论:该病例强调了在出现重叠炎症条件的患者中及时识别PAPASH综合征的重要性,并强调了临床警惕、及时启动生物制剂和协调护理的必要性,以改善这种罕见但严重的疾病的预后。
{"title":"PAPASH Syndrome: A Case Report and Lessons for Clinical Practice.","authors":"Janvi Patel, Farzana Hoque","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Introduction: </strong>PAPASH spectrum syndrome is a rare autoinflammatory condition encompassing psoriatic arthritis, pyoderma gangrenosum, acne, and hidradenitis suppurativa. Despite the individual prevalence of these conditions, their concurrent manifestation poses a diagnostic challenge that requires high clinical suspicion. This case illustrates the consequences of delayed recognition of this condition and underscores the crucial need for a multidisciplinary approach to optimize management.</p><p><strong>Case presentation: </strong>We report the case of a 34-year-old African American man with a prior diagnosis of rheumatoid arthritis who developed migratory arthritis, pustular acne, and hidradenitis suppurativa. Despite suggestive clinical features, delayed access to biologic therapy contributed to disease progression and resulted in hospitalization. After extensive genetic and clinical evaluation, he was diagnosed with PAPASH syndrome.</p><p><strong>Discussion: </strong>PAPASH syndrome is linked to mutations in the PSTPIP1 gene and the overexpression of specific chemokines, which dysregulate interleukin-1 signaling and cause persistent inflammation. Although tumor necrosis factor-α inhibitors remain first-line therapy, limited literature exists on comprehensive treatment strategies, and further research is needed. This case demonstrates how ongoing diagnostic ambiguity and the absence of clear treatment guidelines can complicate the management of PAPASH syndrome.</p><p><strong>Conclusions: </strong>This case emphasizes the importance of prompt identification of PAPASH syndrome in patients presenting with overlapping inflammatory conditions and highlights the need for clinical vigilance, timely initiation of biologic agents, and coordinated care to improve outcomes in this rare but serious disorder.</p>","PeriodicalId":94268,"journal":{"name":"WMJ : official publication of the State Medical Society of Wisconsin","volume":"124 5","pages":"492-495"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145919694","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Spontaneous Splenic Hemorrhage Leading to Diagnosis of Metastatic Adenocarcinoma of Unknown Origin. 自发性脾出血导致不明来源转移性腺癌的诊断。
Morgan Lucero, Jordan Palmer, Shivani Kumar, Pinky Jha

Introduction: Spontaneous splenic hemorrhage is a rare initial presentation of malignancy. The objective of this case report is to elucidate the complexities of early diagnosis of splenic metastases and the complications associated with advanced malignancies of the spleen. It is also a reminder to consider splenic metastases and hemorrhage in the differential diagnosis for nonspecific presentations, such as acute abdomen, in adults.

Case presentation: A 58-year-old female with 1 month of vague, worsening systemic symptoms and computed tomography findings suspicious for a subcapsular splenic hematoma was found to have splenic rupture. After undergoing emergency laparotomy with splenectomy, pathological samples revealed metastatic poorly differentiated adenocarcinoma of unknown origin. During a subsequent admission, she was found to be hemodynamically unstable, deemed a poor candidate for inpatient chemotherapy, and elected to proceed with comfort measures after which she died from multiorgan failure 3 weeks after initial presentation.

Discussion: Spontaneous (nontraumatic) splenic hemorrhage secondary to metastasis should remain a differential diagnosis for patients with acute abdomen and associated risk factors for primary malignancies.

摘要自发性脾出血是一种罕见的恶性肿瘤的初始表现。本病例报告的目的是阐明脾脏转移早期诊断的复杂性和晚期脾脏恶性肿瘤的并发症。这也提醒我们要考虑脾转移和出血的鉴别诊断非特异性表现,如急腹症,在成人。病例介绍:一名58岁女性,1个月来症状模糊,全身症状恶化,计算机断层扫描发现疑似包膜下脾血肿,发现脾破裂。在接受紧急剖腹手术并脾切除术后,病理样本显示转移性低分化腺癌来源不明。在随后的入院中,发现她血流动力学不稳定,认为不适合住院化疗,并选择继续进行舒适措施,之后她在初次就诊后3周死于多器官衰竭。讨论:继发于转移的自发性(非外伤性)脾出血仍应作为急腹症及原发性恶性肿瘤相关危险因素患者的鉴别诊断。
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引用次数: 0
Wisconsin Young Adults' Attitudes, Beliefs, Motivations, and Behaviors Surrounding E-Cigarette Use and Cessation. 威斯康星州年轻人对电子烟使用和戒烟的态度、信念、动机和行为。
Jesse T Kaye, Brian S Williams, Jennifer Bird, Karen L Conner, Rob Adsit, Megan E Piper

Introduction: Electronic cigarette (e-cigarette) use is prevalent among young adults, yet cessation treatment options are limited and underutilized.

Methods: Wisconsin residents aged 18 to 24 who had vaped nicotine in the past month (N = 480) completed an online survey assessing vaping initiation, past quit experiences, future quit intentions, and treatment knowledge and preferences. The survey also assessed perceived physical and mental health harms of vaping nicotine and other products (eg, cannabis, cannabidiol).

Results: Most young adults had made a prior e-cigarette quit attempt, commonly motivated by concerns about addiction, cost, and health problems. Though 80% want support to quit, preferred methods of support were highly variable. The same methods (eg, medication, friends/family, health care provider, therapist) that were most endorsed as the form of support young adults were most likely to use were also among the most endorsed forms of support that young adults would not want to use. Nearly 40% of participants reported vaping cannabis and perceived vaping cannabis as significantly less harmful than vaping nicotine or tobacco for physical and mental health.

Conclusions: Vaping cessation resources that are responsive to young adults' needs and preferences are needed. The high variability in treatment preferences suggests that multiple strategies need to be offered; there is no one-size-fits-all approach. Cannabis vaping is prevalent, and an important area for future research is to examine the impact of cannabis vaping on nicotine vaping dependence, cessation, and treatment use. Strategies to reach, motivate, and engage young adults in e-cigarette cessation and cessation treatment should highlight their concerns about addiction, costs, health harms, and desired treatment options.

电子烟(电子烟)的使用在年轻人中很普遍,但戒烟治疗选择有限且未得到充分利用。方法:威斯康星州年龄在18 - 24岁的480名在过去一个月内吸过尼古丁的居民完成了一项在线调查,评估了吸电子烟的开始、过去的戒烟经历、未来的戒烟意图、治疗知识和偏好。该调查还评估了尼古丁和其他产品(如大麻、大麻二酚)对身心健康的危害。结果:大多数年轻人之前都曾尝试过戒烟,通常是出于对上瘾、成本和健康问题的担忧。虽然80%的人希望支持戒烟,但支持的首选方法变化很大。同样的方法(例如,药物、朋友/家人、卫生保健提供者、治疗师)被认为是年轻人最可能使用的支持形式,也是年轻人最不愿意使用的支持形式。近40%的参与者报告称吸食大麻,并认为吸食大麻对身心健康的危害明显小于吸食尼古丁或烟草。结论:需要满足年轻人需求和偏好的戒烟资源。治疗偏好的高度可变性表明需要提供多种策略;没有放之四海而皆准的方法。吸食大麻很普遍,未来研究的一个重要领域是研究吸食大麻对尼古丁依赖、戒烟和治疗使用的影响。达到、激励和吸引年轻人戒烟和戒烟治疗的策略应突出他们对成瘾、成本、健康危害和所需治疗方案的关注。
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引用次数: 0
A Case of Norwegian Scabies in a Kidney Transplant Patient. 肾移植患者患挪威疥疮一例。
Khaing Wei, Sara Shalin, Venkata R Manchala

Introduction: Crusted scabies (Norwegian scabies) is a rare and severe presentation of skin infestation caused by the mite Sarcoptes scabiei in patients with compromised cellular immunity. Kidney transplant patients are maintained on immunosuppressive agents, which induce impaired T cell immune response that can lead to increased risk of crusted scabies.

Case presentation: We report a case of crusted scabies in a kidney transplant patient who presented with a diffuse skin rash. Diagnosis was delayed and misdiagnosed initially, with subsequent skin biopsy leading to an accurate diagnosis and complete recovery with definitive treatment.

Discussion: Unlike classical scabies, crusted scabies can occur in an atypical pattern that can be misdiagnosed as common skin lesions, and a skin biopsy is crucial to obtain an accurate diagnosis to receive definitive treatment.

Conclusions: Transplant recipients are at an increased risk of severe parasitic infections such as crusted scabies due to drug-induced impairment of their cell-mediated immune response, thus maintaining a high index of suspicion for crusted scabies as a differential diagnosis in transplant kidney patients is extremely important. Early histological diagnosis of crusted scabies is essential to prevent delayed or missed diagnosis and avoid unnecessary serious complications. The combination of an oral ivermectin and topical permethrin regimen resulted in excellent clinical outcomes in our case and is recommended as the standard treatment.

简介:结痂性疥疮(挪威疥疮)是一种罕见而严重的皮肤感染,由疥螨引起,患者细胞免疫功能受损。肾移植患者需要使用免疫抑制剂,这会导致T细胞免疫反应受损,从而增加结痂性疥疮的风险。病例介绍:我们报告一例结痂疥疮在肾移植患者谁提出了漫漫性皮疹。最初的诊断被延误和误诊,随后的皮肤活检导致准确的诊断和完全恢复与明确的治疗。讨论:与经典疥疮不同,结痂性疥疮可能以非典型模式发生,可能被误诊为常见的皮肤病变,皮肤活检对于获得准确诊断以接受明确治疗至关重要。结论:由于药物诱导的细胞免疫反应受损,移植受者发生严重寄生虫感染(如结痂性疥疮)的风险增加,因此在移植肾患者中,保持对结痂性疥疮的高度怀疑指数作为鉴别诊断是非常重要的。结痂性疥疮的早期组织学诊断对于预防延误或漏诊以及避免不必要的严重并发症至关重要。在我们的病例中,口服伊维菌素和外用氯菊酯方案的联合治疗取得了良好的临床效果,并被推荐为标准治疗。
{"title":"A Case of Norwegian Scabies in a Kidney Transplant Patient.","authors":"Khaing Wei, Sara Shalin, Venkata R Manchala","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Introduction: </strong>Crusted scabies (Norwegian scabies) is a rare and severe presentation of skin infestation caused by the mite <i>Sarcoptes scabiei</i> in patients with compromised cellular immunity. Kidney transplant patients are maintained on immunosuppressive agents, which induce impaired T cell immune response that can lead to increased risk of crusted scabies.</p><p><strong>Case presentation: </strong>We report a case of crusted scabies in a kidney transplant patient who presented with a diffuse skin rash. Diagnosis was delayed and misdiagnosed initially, with subsequent skin biopsy leading to an accurate diagnosis and complete recovery with definitive treatment.</p><p><strong>Discussion: </strong>Unlike classical scabies, crusted scabies can occur in an atypical pattern that can be misdiagnosed as common skin lesions, and a skin biopsy is crucial to obtain an accurate diagnosis to receive definitive treatment.</p><p><strong>Conclusions: </strong>Transplant recipients are at an increased risk of severe parasitic infections such as crusted scabies due to drug-induced impairment of their cell-mediated immune response, thus maintaining a high index of suspicion for crusted scabies as a differential diagnosis in transplant kidney patients is extremely important. Early histological diagnosis of crusted scabies is essential to prevent delayed or missed diagnosis and avoid unnecessary serious complications. The combination of an oral ivermectin and topical permethrin regimen resulted in excellent clinical outcomes in our case and is recommended as the standard treatment.</p>","PeriodicalId":94268,"journal":{"name":"WMJ : official publication of the State Medical Society of Wisconsin","volume":"124 2","pages":"187-191"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144683918","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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