發(fā)布時(shí)間：2018-05-24 10:19

  本文選題：銀屑病 + 血小板增多癥　； 參考：《臨床皮膚科雜志》2017年09期

【摘要】：報(bào)告1例兒童尋常性銀屑病并發(fā)血小板增多癥�；純耗�,7歲。軀干及四肢散在紅斑、鱗屑1個(gè)月。皮膚科檢查:軀干、腹部、四肢散在分布紅斑、丘疹,上覆少量銀白色鱗屑,薄膜現(xiàn)象及Auspitz征陽性。皮損組織病理:表皮角化過度伴輕度角化不全,棘層肥厚,表皮突延長,真皮乳頭上方表皮層變薄;血常規(guī)示血小板計(jì)數(shù)1249×l09/L;骨髓穿刺:骨髓增生極度活躍,全片共見巨核細(xì)胞1650個(gè),血小板成堆可見。診斷:兒童尋常型銀屑病并發(fā)血小板增多癥。
[Abstract]:A case of psoriasis vulgaris complicated with thrombocytosis in children was reported. The boy was 7 years old. Torso and limbs scattered in erythema, scales for 1 month. Dermatology examination: torso, abdomen, limbs scattered erythema, papules, coated with a small amount of silvery white scales, membrane phenomenon and Auspitz sign positive. Histopathology: hyperkeratosis of epidermis with mild keratosis, hypertrophy of spinous layer, lengthening of epidermis, thinning of epidermis above dermal papilla, platelet count of 1249 脳 10 9 / L, bone marrow puncture, hyperactivity of bone marrow hyperplasia, There were 1650 megakaryocytes and platelets in piles. Diagnosis: psoriasis vulgaris complicated with thrombocytosis in children.
【作者單位】： 河北工程大學(xué)附屬醫(yī)院皮膚科;河北工程大學(xué)附屬醫(yī)院血液科;
【分類號(hào)】：R758.63
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本文編號(hào)：1928698