Girault D, Goulet O, Le Deist F, Brousse N, Colomb V, Césarini J P, de Potter S, Canioni D, Griscelli C, Fischer A
Hematology and Immunology Unit, Inserm U 132, Paris, France.
J Pediatr. 1994 Jul;125(1):36-42. doi: 10.1016/s0022-3476(94)70118-0.
We report on eight children with severe diarrhea beginning in the first 6 months of life (< 1 month in six cases), who had a number of features in common. All were small for gestational age and had an abnormal phenotype, including facial dysmorphism, hypertelorism, and woolly, easily removable hair with trichorhexis nodosa. Two were products of consanguineous marriages. Severe secretory diarrhea persisted despite bowel rest (n = 7). Jejunal biopsy specimens showed total or subtotal villous atrophy with crypt necrosis, and inconstant T-cell activation in some cases (n = 3). Colon biopsy specimens showed moderate nonspecific colitis. All the patients had defective antibody responses despite normal serum immunoglobulin levels, and defective antigen-specific skin tests despite positive proliferative responses in vitro. Three had monoclonal hyper-immunoglobulinemia A. The course was marked by diffuse erythroderma in two cases and mental retardation in three. Treatment included bowel rest, intravenous administration of immune globulins, administration of corticosteroids (n = 6) and cyclosporine (n = 2), and bone marrow transplantation (n = 1). Five patients died between the ages of 2 and 5 years (of sepsis or cirrhosis), two are being fed enterally, and one continues to receive total parenteral nutrition. The cause of the combined low birth weight, dysmorphism, severe diarrhea, trichorrhexis, and immunodeficiency is unclear. These features may constitute a specific syndrome within the group of intractable diarrheas of infancy.
我们报告了8名在出生后头6个月内开始出现严重腹泻的儿童(6例在出生后<1个月),他们有一些共同特征。所有患儿均小于胎龄,且有异常表型,包括面部畸形、眼距增宽,以及有结节性脆发的羊毛状、易于拔除的毛发。其中2例为近亲结婚的后代。尽管进行了肠道休息,严重的分泌性腹泻仍持续存在(n = 7)。空肠活检标本显示完全或部分绒毛萎缩伴隐窝坏死,部分病例(n = 3)有不恒定的T细胞活化。结肠活检标本显示中度非特异性结肠炎。所有患者尽管血清免疫球蛋白水平正常,但抗体反应存在缺陷,尽管体外增殖反应阳性,但抗原特异性皮肤试验存在缺陷。3例有单克隆高免疫球蛋白A血症。病程特点为2例出现弥漫性红皮病,3例出现智力发育迟缓。治疗包括肠道休息、静脉注射免疫球蛋白、使用皮质类固醇(n = 6)和环孢素(n = 2),以及进行骨髓移植(n = 1)。5例患者在2至5岁之间死亡(死于败血症或肝硬化),2例接受肠内喂养,1例继续接受全胃肠外营养。出生体重低、畸形、严重腹泻、脆发和免疫缺陷合并出现的原因尚不清楚。这些特征可能构成婴儿期难治性腹泻组中的一种特定综合征。