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Perforating neutrophilic and granulomatous dermatitis of the newborn--a clue to immunodeficiency.

机译:新生儿穿孔中性粒细胞肉芽肿性皮炎-免疫缺陷的线索。

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摘要

We report two newborns with a widespread cutaneous eruption consisting of discrete papules which evolved into vesicles, pustules, crusts, and ulcers. These healed over a 2-week period with scarring. Histopathology showed three main features--histiocytic granulomas, neutrophilic infiltration, and transepidermal elimination of degenerated collagen and debris through hair follicles. Both patients had congenital immunodeficiency. This skin condition of the newborn, with distinct clinical and histopathologic features, is a manifestation of immunodeficiency that has not been previously described.
机译:我们报道了两个新生儿,皮肤由广泛的皮疹组成,由不连续的丘疹组成,逐渐演变为囊泡,脓疱,结rust和溃疡。这些在两周内愈合,并留下疤痕。组织病理学显示出三个主要特征-组织细胞肉芽肿,嗜中性粒细胞浸润和经皮通过毛囊消除变性胶原蛋白和碎屑。两名患者均患有先天性免疫缺陷。新生儿的这种皮肤状况具有独特的临床和组织病理学特征,是免疫缺陷的表现,以前没有描述过。

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