Obara Koji
Neurology, National Hospital Organization Akita National Hospital, Yurihonjo, JPN.
Cureus. 2023 Apr 17;15(4):e37669. doi: 10.7759/cureus.37669. eCollection 2023 Apr.
Adrenoleukodystrophy (ALD) is a rare X-linked disease that affects the metabolism of very long-chain fatty acids (VLCFAs), leading to cognitive deterioration, progressive spastic paraplegia, sensory disturbance, adrenocortical insufficiency, and bladder and bowel abnormalities. Although the symptoms of ALD correspond to the risk of developing pressure ulcers, a pressure ulcer has never been listed as a complication of ALD. We present two cases of ALD with severe pressure ulcers in the pelvic region and feet. The first case was a 27-year-old male patient with adolescent cerebral-type ALD who had pressure ulcers with bone exposure on the sacral and bilateral greater trochanter region. The second case was a 64-year-old male patient with adrenomyeloneuropathy (AMN) phenotype who had pressure ulcers on the sacral region and both feet. Both patients had VLCFA accumulation and a likely pathogenic variant in the gene, the causative gene of ALD. These cases indicate that ALD patients with immobility and incontinence have a higher risk of developing severe pressure ulcers, which requires the proactive identification of ALD patients and early multidisciplinary intervention for patients and their families to prevent the development of pressure ulcers.
肾上腺脑白质营养不良(ALD)是一种罕见的X连锁疾病,会影响极长链脂肪酸(VLCFA)的代谢,导致认知功能衰退、进行性痉挛性截瘫、感觉障碍、肾上腺皮质功能不全以及膀胱和肠道异常。尽管ALD的症状与发生压疮的风险相关,但压疮从未被列为ALD的并发症。我们报告两例ALD患者,其在骨盆区域和足部出现严重压疮。第一例是一名27岁男性患者,患有青少年脑型ALD,在骶骨和双侧大转子区域出现了伴有骨质外露的压疮。第二例是一名64岁男性患者,具有肾上腺脊髓神经病(AMN)表型,在骶骨区域和双足出现压疮。两名患者均存在VLCFA蓄积,且在ALD致病基因 中存在一个可能的致病变异。这些病例表明,行动不便和大小便失禁的ALD患者发生严重压疮的风险更高,这需要主动识别ALD患者,并对患者及其家属进行早期多学科干预,以预防压疮的发生。