Cianciulli P, Sorrentino F, Maffei L, Amadori S, Cappabianca M P, Foglietta E, Carnevali E, Pasquali-Ronchetti I
Ospedale S. Eugenio, Day Hospital Talassemie, P.le dell'Umanesimo 10, 00143 Rome, Italy.
Eur J Clin Invest. 2002 Sep;32(9):700-6. doi: 10.1046/j.1365-2362.2002.01032.x.
Congenital haemolytic anaemia may be associated with pseudoxanthoma elasticum (PXE)-like clinical manifestations.
The cardiovascular system of 14 homozygous and double heterozygous beta-thalassaemia patients with skin and retinal vessel alterations similar to those in genetic PXE was analysed over a period of 12 years and compared with that of 13 relatives (five sets of parents, one single parent, two thalassaemic brothers), and that of the control group composed of 16, age- and sex-matched, thalassaemic patients.
All patients with clinical PXE-like skin lesions exhibited, by light and electron microscopy, dermal alterations and mineralization of elastic fibres identical to those typical of inherited PXE. None of the relatives and none of the control group showed clinical or structural findings of PXE. The follow-up started in 1988. After 12 years of clinical observation, six patients showed dramatic progression of skin involvement, angioid streaks had progressed in two subjects. One patient had recurrent gastrointestinal bleeding and underwent partial stomach removal for gastric artery aneurysm, one underwent colon resection for intestinal infarct, one patient had a transitory ischaemic attack, one died after an intracranial haemorrhage, two patients died from cardiovascular disease and one from neoplasia.
Thalassaemic patients with PXE-like skin lesions also manifest PXE-like vessel alterations that progress with time. Considering the severe outcome of these lesions, accurate monitoring should be routinely performed on the cardiovascular system of thalassaemic patients with PXE-like skin manifestations.
先天性溶血性贫血可能与弹性假黄瘤(PXE)样临床表现相关。
对14例纯合子和双杂合子β地中海贫血患者的心血管系统进行了为期12年的分析,这些患者的皮肤和视网膜血管改变与遗传性PXE相似,并与13名亲属(5对父母、1名单亲、2名地中海贫血兄弟)以及由16名年龄和性别匹配的地中海贫血患者组成的对照组进行比较。
所有具有临床PXE样皮肤病变的患者,通过光镜和电镜检查,均表现出真皮改变和弹性纤维矿化,与遗传性PXE的典型表现相同。亲属和对照组均未显示PXE的临床或结构特征。随访始于1988年。经过12年的临床观察,6例患者皮肤受累情况显著进展,2例患者的血管样条纹有所进展。1例患者反复出现胃肠道出血,因胃动脉瘤接受了部分胃切除术,1例因肠梗死接受了结肠切除术,1例患者发生短暂性脑缺血发作,1例患者颅内出血后死亡,2例患者死于心血管疾病,1例死于肿瘤。
具有PXE样皮肤病变的地中海贫血患者也表现出随时间进展的PXE样血管改变。鉴于这些病变的严重后果,对于有PXE样皮肤表现的地中海贫血患者,应常规对其心血管系统进行精确监测。