Sendhil Kumaran Muthu, Dutta Pinaki, Sakia Uma, Dogra Sunil
Department of Dermatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Department of Endocrinology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Int J Dermatol. 2015 Aug;54(8):e280-6. doi: 10.1111/ijd.12658. Epub 2015 May 27.
Pretibial myxedema (PTM) is a rare manifestation of Graves' disease. There is paucity of data regarding long-term follow-up and response to treatment in PTM.
Retrospective study wherein 30 patients of PTM presenting during 2001-2011 attending dermatology and endocrinology outpatient departments were analyzed.
Among 30 patients with PTM, 12 were males and 18 females with a ratio of 1 : 1.5 males/females. Four morphological forms were identified: plaques (18 patients), diffuse non-pitting edema of both lower legs (five), nodules (five), and elephantiasis lesions (two). Eighty percent were diagnosed with hyperthyroidism before the development of dermopathy. Twenty-six patients presented with ophthalmopathy. Fourteen patients with plaque had an excellent response to topical clobetasol propionate ointment and attained complete resolution by 3.6 years. Out of 16 patients treated with combination therapy, which included nine treated with topical corticosteroids/intralesional triamcinolone and seven treated with oral, intralesional, and topical corticosteroids, nine attained complete resolution in the lesions by 3.4 years, and none relapsed anytime during four years of post-treatment follow-up. However, the remaining patients (elephantiasis and diffuse forms) failed to achieve complete resolution.
Plaques and nodules are common variants with a favorable clinical response to topical and intralesional corticosteroid; elephantine and diffuse forms responded poorly to therapy. Studies analyzing larger cohorts of patients with PTM and their long-term follow-up are limited, hence more such studies are required.
胫前黏液性水肿(PTM)是格雷夫斯病的一种罕见表现。关于PTM的长期随访和治疗反应的数据较少。
进行回顾性研究,分析了2001年至2011年期间在皮肤科和内分泌科门诊就诊的30例PTM患者。
在30例PTM患者中,男性12例,女性18例,男女比例为1∶1.5。确定了四种形态学类型:斑块型(18例)、双侧小腿弥漫性非凹陷性水肿型(5例)、结节型(5例)和象皮病型(2例)。80%的患者在皮肤病发生前被诊断为甲状腺功能亢进。26例患者出现眼病。14例斑块型患者外用丙酸氯倍他索软膏反应良好,3.6年后完全消退。在16例接受联合治疗的患者中,9例接受外用糖皮质激素/病灶内注射曲安奈德治疗,7例接受口服、病灶内注射和外用糖皮质激素治疗,9例在3.4年后病灶完全消退,在治疗后四年的随访期间均未复发。然而,其余患者(象皮病型和弥漫型)未能完全消退。
斑块型和结节型是常见类型,对外用和病灶内注射糖皮质激素有良好的临床反应;象皮病型和弥漫型对治疗反应较差。分析更大队列的PTM患者及其长期随访的研究有限,因此需要更多此类研究。