A rare, unusually acute presentation of denervation pseudohypertrophy [0.03%]
一种少见的神经元缺失假性肥大的急性表现形式病例报告
Monica Botross,Amirmohammad Shafiee,Lisa Couch et al.
Monica Botross et al.
Denervation pseudohypertrophy is an important and well described, albeit rare, cause of limb swelling that is seldom encountered in the clinical setting. Careful history taking, reasonable clinical suspicion, and referral for magnetic reson...
Liang Luo,Yun Huang,Xin-Tao Wang et al.
Liang Luo et al.
Ceruminous adenocarcinoma (CAC) represents an exceedingly rare malignant glandular neoplasm originating from the ceruminous glands within the external auditory canal (EAC), constituting approximately 5%-10% of all EAC malignancies. Owing to...
Acromegaly-induced dilated cardiomyopathy presenting with heart failure as the cardinal symptom: A case report [0.03%]
肢端肥大症诱发的心肌病以心力衰竭为主要症状：病例报告
Jiamin Xu,Jie Liu,Heng Wu et al.
Jiamin Xu et al.
Acromegaly is a rare endocrine disorder caused by excessive secretion of growth hormone, resulting in elevated serum levels of hepatic insulin-like growth factor-1 (IGF-1). With an estimated annual incidence of approximately three cases per...
Effects of non-invasive multimodal transcutaneous electrotherapy on pain and posture associated with lumbar radicular pain: A case series [0.03%]
无创多模态透皮电疗对单侧腰椎坐骨神经痛患者疼痛及姿势影响的病例系列研究
Giovanni Barassi,Loris Prosperi,Marco Supplizi et al.
Giovanni Barassi et al.
Radicular lumbar pain is a widespread condition characterized by nerve dysfunction. Many treatments have been proposed over time for its management, ranging from surgery to conservative approaches. The combined application of multiple trans...
Gabriele Perazzolli,Elia Banchetti,Enrico Melis et al.
Gabriele Perazzolli et al.
Chilblain lupus erythematosus is a rare, cold-induced form of chronic cutaneous lupus that can occur in both genetic and sporadic forms. It is characterized by acral skin lesions and is commonly associated with autoimmunity and type I inter...
Dupilumab improves itch, but not fibrosis, in a patient with scleromyxedema: A case report [0.03%]
杜普利尤单抗改善了硬红斑样黏蛋白病患者的瘙痒但不能改善纤维化：1例报告
Katya Peri,Naila Bouadi,Anna Nikonova et al.
Katya Peri et al.
Scleromyxedema is a rare, chronic mucinosis characterized by widespread skin fibrosis and an associated monoclonal gammopathy. Therapeutic options remain limited. We present the case of a male in his 50s with biopsy-confirmed scleromyxedema...
First identification of the rare FH-Q185R germline mutation in a Chinese HLRCC patient: A case report and literature review [0.03%]
中国HLRCC患者中FH突变型(Q185R)首次鉴定：病例报告及文献回顾
Lu Zhang,Ge Gao,Mengrui Yuan et al.
Lu Zhang et al.
Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) is a rare autosomal dominant disorder caused by the fumarate hydratase (FH) gene mutations. Here, we report the first identification of the rare FH-Q185R mutation in a Chinese patient ...
Kaitlyn Rourke,Aneesh Karir,Marni C Wiseman et al.
Kaitlyn Rourke et al.
Many individuals with localized melanoma undergo wide local excision and live many years with the surgical scar. The present case describes a basal cell carcinoma arising from a malignant melanoma excision scar. There are no similar reports...
A case report on the integration of the Monitored Augmented Rehabilitation System in a multidisciplinary rehabilitation program for a pediatric patient with a ruptured arteriovenous malformation [0.03%]
蒙特梭利增强康复系统在儿童动脉瘤破裂后的综合康复治疗中的应用案例报告
Samuel T Lauman,Shreya Ravi,Kara Chaplin et al.
Samuel T Lauman et al.
Cerebral arteriovenous malformations (AVMs) are congenital vascular abnormalities that can lead to neurological impairments following rupture. This proof-of-concept case report examines the integration of the Monitored Augmented Rehabilitat...
Clozapine use in an adolescent with comorbid diagnoses of autism spectrum disorder, schizoaffective disorder, moderate intellectual disability, and severe behavioral dysregulation: A case report [0.03%]
合并自闭症谱系障碍、心境分裂性障碍、中度智力障碍和严重行为失调的青少年使用氯氮平治疗：病例报告
Pamela Ralph,Shannon See,Allison Faust
Pamela Ralph
In this case report, we present the first 14 months of an 18-year-old adolescent male with comorbid diagnoses who exhibits extremely aggressive and self-injurious behavior and is treated with a combination of clozapine and behavioral interv...