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A case of systemic amyloidosis beginning with purpura 被引量:2
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作者 Zhao Jun-ying Zhang Rui-na +3 位作者 Duan Xiao-han Xu Zhi-li Li Hong-wei gu fu-sheng 《Chinese Medical Journal》 SCIE CAS CSCD 2012年第3期555-557,共3页
Primary systemic amyloidosis is a relatively rare disease, caused when abnormal extracellular deposition of fibrillary protein builds up in a variety of target organs, such as heart, kidneys, lungs liver, and so forth... Primary systemic amyloidosis is a relatively rare disease, caused when abnormal extracellular deposition of fibrillary protein builds up in a variety of target organs, such as heart, kidneys, lungs liver, and so forth. The symptoms of the disease are usually vague, while many kinds of auxiliary or laboratory examinations especially pathologic biopsy can provide a clue for the diagnosis. Here we described a case who had purpura-like lesions in the initial stage, followed by progressive malfunctions in the kidneys, the heart, the lungs, as wel~ as the liver. The final diagnosis was primary systemic amyloidosis determined by skin pathologic biopsy. And the disease led to a fatal outcome within three months after the diagnosis. 展开更多
关键词 primary systemic amyloidosis Congo red stain PURPURA
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