[Elephantiasic pretibial myxoedema: study of five cases].

Dakar medical Pub Date : 2007-01-01
S O Niang, M Diallo, A Kane, T I Bocoum, M T Dieng, B Ndiaye
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Abstract

Introduction: Elephantiasic myxoedema is very rare. We report 5 pretibial myxoedema cases observed in the Dermatological department of Le Dantec hospital in Dakar.

Patients and methods: Our 5 cases were 3 women (age: 52, 45 and 18 years) and 2 men (age: 54 and 32 years).

Results: All the cases were enormous, multinodular pachydermic, bilateral, elephantiasis in the low leg and associated to Graves 'disease. The duration was 4 month to 12 year. In 3 cases there was a Diamond syndrome which is a severe form. The cutaneous lesions were not influenced by medical treatment of thyroid disease. Systemic steroids achieved improvement of the elephantiasis in 1 case.

Conclusion: Elephantiasis is a very unusual presentation of pretibial myxoedema and its occurrence doesn't depend to the intensity of thyrotoxicosis and its evolution. However in our cases, it was a severity indicator factor, like Diamond syndrome. Local and systemic steroids give very rarely improvement.

象皮性胫前黏液水肿5例分析
象皮性黏液水肿非常罕见。我们报告在达喀尔勒丹特克医院皮肤科观察到的5例胫骨前黏液水肿病例。患者和方法:5例患者,女性3例,年龄分别为52岁、45岁和18岁,男性2例,年龄分别为54岁和32岁。结果:所有病例均为巨大、多结节性厚皮病、双侧、下肢象皮病,并伴有Graves病。病程从4个月到12年不等。其中3例有严重的戴蒙德综合症。皮肤病变不受甲状腺疾病药物治疗的影响。全身类固醇治疗改善1例象皮病。结论:象皮病是胫前黏液水肿的一种罕见表现,其发生与甲状腺毒症的严重程度及其进展无关。但在我们的病例中,这是一个严重的指标因素,就像戴蒙德综合症一样。局部和全身类固醇很少有改善作用。
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