Deal J E, Groves R W, Harmer A W, Welsh K I, MacDonald D M, Rigden S P
Department of Paediatric Nephrology, Guy's Hospital, London SE1 9RT.
BMJ. 1991 Jul 20;303(6795):161-3. doi: 10.1136/bmj.303.6795.161.
To describe the association between epithelial cell IgM, which has previously been associated with an increased incidence of loss of renal graft in children, with a novel cutaneous eruption and unexplained native renal disease.
Observational study on children with epithelial cell antibody presenting with unexplained renal or skin disease.
General paediatric department and regional paediatric nephrology unit.
Six children (five girls, one boy), who presented to the unit in 1989-90.
Three children, two of whom had a history of a hyperpigmented rash, presented with hypertension, proteinuria, and impaired renal function. Renal biopsy specimens from two of these children showed severe arteriolar endothelial cell swelling with arteriolar occlusion. These children fully recovered after treatment with antihypertensive drugs. The third child developed end stage renal failure and required dialysis. Three other children presented with an unusual cutaneous eruption but no evidence of renal disease. Histology of the skin lesions showed acute epidermal necrosis and features consistent with a viral infection.
The aetiology and pathogenesis of the epithelial cell antibody are unknown. These cases indicate that it may have a role in native kidney disease and focal epidermal necrosis. Clinical and histological features suggest that the antibody may be associated with a viral infection.
描述上皮细胞免疫球蛋白M(此前已发现其与儿童肾移植丢失发生率增加有关)与一种新型皮疹及不明原因的自身肾病之间的关联。
对患有上皮细胞抗体且伴有不明原因肾病或皮肤病的儿童进行观察性研究。
普通儿科和地区儿科肾病科。
1989年至1990年期间到该科室就诊的6名儿童(5名女孩,1名男孩)。
3名儿童,其中2名有色素沉着皮疹病史,出现高血压、蛋白尿和肾功能受损。这3名儿童中的2名的肾活检标本显示严重的小动脉内皮细胞肿胀伴小动脉闭塞。这些儿童经抗高血压药物治疗后完全康复。第3名儿童发展为终末期肾衰竭,需要透析。另外3名儿童出现一种不寻常的皮疹,但无肾病证据。皮肤病变组织学显示急性表皮坏死及与病毒感染相符的特征。
上皮细胞抗体的病因和发病机制尚不清楚。这些病例表明其可能在自身肾病和局灶性表皮坏死中起作用。临床和组织学特征提示该抗体可能与病毒感染有关。