Bronson D M, Barsky R, Barsky S
J Am Acad Dermatol. 1983 Jul;9(1):140-4. doi: 10.1016/s0190-9622(83)70120-9.
A case of acrodermatitis enteropathica belatedly recognized in a pregnant 23-year-old woman is reported. The condition was not specifically diagnosed during childhood. It cleared at puberty but recurred during two of three pregnancies in the form of pustular, vesiculobullous, and psoriasiform lesions. There were no associated signs or symptoms in other organs. Initial diagnoses upon the recurrence during the third pregnancy were herpes gestationis and impetigo herpetiformis. A markedly decreased serum zinc level (18 micrograms/dl) was found. Treatment with zinc sulfate was instituted, and within 3 days the cutaneous lesions began to clear. Two months after the birth of a healthy child, and without further therapy, all lesions had resolved and the serum zinc level was nearly normal. Acrodermatitis enteropathica should be considered in the differential diagnosis of unresponsive bullous dermatoses occurring during pregnancy.
报告了一例在一名23岁孕妇中迟发性诊断的肠病性肢端皮炎病例。该疾病在儿童期未得到明确诊断。青春期时病情缓解,但在三次怀孕中有两次复发,表现为脓疱、水疱大疱和银屑病样皮损。其他器官无相关体征或症状。第三次怀孕复发时最初诊断为妊娠疱疹和疱疹样脓疱病。发现血清锌水平显著降低(18微克/分升)。给予硫酸锌治疗,3天内皮肤损害开始消退。在健康婴儿出生两个月后,未经进一步治疗,所有皮损均已消退,血清锌水平接近正常。在妊娠期间出现的难治性大疱性皮肤病的鉴别诊断中应考虑肠病性肢端皮炎。