急性移植物抗宿主病的皮肤表现:临床和病理分析。

M L Hsu, Y C Chen, Y C Wu, C L Chen, H P Yeh, K H Hsieh, Y C Lu
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引用次数: 0

摘要

我们报告11例急性移植物抗宿主病(GVHD);10例发生在骨髓移植(BMT)后,1例发生在严重联合免疫缺陷(SCID)患者输注未辐照全血后。根据西雅图分级,III级5例,II级2例,i级4例。在移植或输血后第6 ~ 47天(22 +/- 12天)出现皮疹,最初通常表现为颈部或上胸部出现红斑斑或丘疹。皮疹在结垢时消退,严重者变为紫癜、色素沉着或红皮病。皮肤病理分级与GVHD的临床严重程度相关。5例晚期GVHD (III级)患者中有4例死亡。除一例(SCID病例)外,其余4例患者的皮肤病理均表现为广泛的基底空泡化和多发角化异常细胞。其他轻度或局灶性基底空泡化和少量角化异常细胞均未进展为晚期GVHD。5例晚期GVHD患者中有3例环孢素a剂量不足,提示严重GVHD预后不良,适当剂量的环孢素a对于减轻GVHD的严重程度和降低死亡率具有重要意义。在皮疹期间进行的血清病毒学研究为阴性,提示BMT后的皮疹主要由GVHD引起,并且总是先于肠道或肝脏表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The skin manifestation of acute graft-versus-host disease: clinical and pathological analysis.

We report 11 cases of acute graft-versus-host disease (GVHD); 10 occurred after bone marrow transplantation (BMT) and one following transfusion of nonirradiated whole blood in a patient with severe combined immunodeficiency (SCID). According to the Seattle Classification, 5 cases were of Grade III, 2 Grade II, and 4 Grade I. The skin rash developed between the 6th to 47th day (22 +/- 12 day) after transplantation or transfusion, and was usually manifested initially as erythematous macules or papules in the neck or upper chest. The rash resolved in scaling or became purpuric, pigmented or erythrodermic in severe cases. The grading of skin pathology correlated well with clinical severity of GVHD. Four of the five who had advanced GVHD (Grade III) died. In all 4 cases but one (the SCID case), the skin pathology showed extensive basal vacuolization and multiple dyskeratotic cells. None of the others with mild or focal basal vacuolization and few dyskeratotic cells progressed into advanced GVHD. Three of the 5 cases with advanced GVHD received an underdose of cyclosporin A. These results suggest that severe GVHD carries a poor prognosis and an adequate dose of cyclosporin A is important in alleviating the severity of GVHD and reducing the mortality. The sero-virologic study performed during the skin rash period was negative, suggesting that the skin rash following BMT is mainly caused by GVHD and always precedes intestinal or hepatic manifestations.

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