Iqbal Fatima, Phan Kevin, Cheung Wah N
Department of Diabetes and Endocrinology, Westmead Hospital, Sydney, New South Wales, Australia.
College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Endocrinol Diabetes Metab Case Rep. 2025 Jan 9;2025(1). doi: 10.1530/EDM-24-0088. Print 2025 Jan 1.
Palmoplantar keratoderma (PPK), characterised by excessive epidermal thickening of the skin on the palms and/or plantar surfaces of the feet, can be hereditary or acquired. Here, we report a case of a 53-year-old woman with a history of sub-optimally controlled diabetes mellitus presenting with fevers and decreased Glasgow Coma Scale (GCS) to a tertiary hospital. She was diagnosed with diabetic ketoacidosis (DKA), with blood glucose at 40 mmol/L and ketones at 7 mmol/L, in the setting of a methicillin-sensitive Staphylococcus aureus necrotising soft tissue back infection. Her medical history included diabetes managed with insulin but no engagement with an endocrinologist or allied health support. Examination revealed an infected, necrotic back wound on her left mid-upper back that required surgical debridement and broad-spectrum IV antibiotics. In addition, she exhibited marked plantar keratoderma and onychogryphosis, reportedly present and worsening over approximately two years. She was prescribed 40% urea cream twice daily, resulting in gradual sloughing of the hyperkeratotic skin within a few weeks. Her HbA1c was 10.4%, and she tested negative for diabetes antibodies, indicating type 2 diabetes. Treatment included an insulin-dextrose infusion until DKA resolved, followed by twice daily insulin degludec/aspart (Ryzodeg 70/30) and metformin. The PPK was attributed likely secondary to sub-optimally managed diabetes.
Diabetes mellitus has multiple complications, including rare dermatologic manifestations such as PPK.This case illustrates the importance of thorough skin assessments in patients with diabetes, particularly those that have a history of sub-optimal diabetes control.A multidisciplinary approach, integrating dermatology, endocrinology and allied health services such as podiatry, is essential in managing diabetes-related complications, improving patient quality of life and preventing further complex manifestations.
掌跖角化病(PPK)的特征是手掌和/或脚底皮肤的表皮过度增厚,可分为遗传性或获得性。在此,我们报告一例53岁女性病例,该患者有糖尿病控制不佳病史,因发热和格拉斯哥昏迷量表(GCS)评分降低入住一家三级医院。她被诊断为糖尿病酮症酸中毒(DKA),血糖为40 mmol/L,酮体为7 mmol/L,同时伴有甲氧西林敏感金黄色葡萄球菌坏死性软组织背部感染。她的病史包括使用胰岛素治疗糖尿病,但未咨询内分泌科医生或接受相关健康支持。检查发现她左中上背部有一处感染坏死性伤口,需要手术清创并使用广谱静脉抗生素。此外,她还表现出明显的掌跖角化病和甲癣,据报道已有约两年时间且病情逐渐加重。她每天两次外用40%尿素霜,几周内角质增生皮肤逐渐脱落。她的糖化血红蛋白(HbA1c)为10.4%,糖尿病抗体检测呈阴性,提示2型糖尿病。治疗包括静脉输注胰岛素 - 葡萄糖直至DKA缓解,随后每天两次注射德谷胰岛素/门冬胰岛素(Ryzodeg 70/30)和二甲双胍。PPK可能归因于糖尿病管理欠佳。
糖尿病有多种并发症,包括罕见的皮肤表现如PPK。该病例说明了对糖尿病患者进行全面皮肤评估的重要性,特别是那些有糖尿病控制不佳病史的患者。多学科方法,整合皮肤科、内分泌科和足病学等相关健康服务,对于管理糖尿病相关并发症、改善患者生活质量和预防进一步复杂表现至关重要。