Lawrence A, Aggarwal A, Misra R
Department of Immunology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, 226 014, India.
Clin Rheumatol. 2007 Feb;26(2):205-7. doi: 10.1007/s10067-006-0276-4. Epub 2006 Apr 6.
Mixed connective tissue disease (MCTD) has been rarely reported from India. Thus, we did a retrospective analysis of cases of MCTD seen at our hospital during the last 13 years. We found 16 cases among 441 patients with connective tissue disease. All the 16 patients (15 females) of MCTD fulfilled classification criteria by Kasukawa and at least one of the other two (Sharp's and Alarcon-Sergovia). Raynaud's phenomenon, sclerodactyly, puffy fingers, esophageal hypomotility, and pulmonary disease were the most common manifestations. At a median follow-up of 12 months (1-172), 12 patients developed features of limited scleroderma and three patients had pulmonary hypertension.
混合性结缔组织病(MCTD)在印度鲜有报道。因此,我们对过去13年在我院就诊的MCTD病例进行了回顾性分析。我们在441例结缔组织病患者中发现了16例。所有16例MCTD患者(15例女性)均符合Kasukawa分类标准以及其他两项标准(Sharp标准和Alarcon-Sergovia标准)中的至少一项。雷诺现象、指端硬化、手指肿胀、食管动力不足和肺部疾病是最常见的表现。在中位随访12个月(1 - 172个月)时,12例患者出现了局限性硬皮病的特征,3例患者患有肺动脉高压。