DERMATITIS AS A PRESENTING SIGN OF CYSTIC-FIBROSIS

被引:42
作者
DARMSTADT, GL
SCHMIDT, CP
WECHSLER, DS
TUNNESSEN, WW
ROSENSTEIN, BJ
机构
[1] JOHNS HOPKINS UNIV HOSP, DEPT DERMATOL, BALTIMORE, MD 21205 USA
[2] CHILDRENS HOSP PHILDELPHIA, PHILADELPHIA, PA USA
关键词
D O I
10.1001/archderm.128.10.1358
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background.-Three percent to 13% of patients with cystic fibrosis present with protein-energy malnutrition that is characterized by hypoproteinemia, edema, and anemia and is associated with high morbidity and mortality. Cutaneous manifestations of malnutrition are rare in patients with cystic fibrosis and have been attributed to deficiencies of protein, zinc, and essential fatty acids. Observations.-We describe five patients who presented with failure to thrive, hypoproteinemia, edema, and a cutaneous eruption before the onset of pulmonary symptoms and before the diagnosis of cystic fibrosis was made. The rash had a predilection for the extremities (lower>upper), perineum, and periorificial surfaces. In most cases, erythematous, scaling papules developed by 4 months of age and progressed within 1 to 3 months to extensive, desquamating plaques. Alopecia was variable, and mucous membrane or nail involvement was not observed. The rash was associated with malnutrition and resolved in all survivors within 10 days of providing pancreatic enzyme and nutritional supplementation. The pathogenesis of the rash is unclear, but it appears to stem from deficiencies of zinc, protein, and essential fatty acids and may be mediated by alterations in prostaglandin metabolism. Conclusions.-Cystic fibrosis should be included in the differential diagnosis of the red, scaly infant, particularly when failure to thrive, hypoproteinemia, and edema are also present. Recognition of rash as a sign of cystic fibrosis complicated by protein-energy malnutrition will allow earlier diagnosis and treatment of these patients and may improve their outcome.
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页码:1358 / 1364
页数:7
相关论文
共 47 条
[1]   HYPOALBUMINEMIA AT DIAGNOSIS AS A MARKER FOR SEVERE RESPIRATORY COURSE IN INFANTS WITH CYSTIC-FIBROSIS IDENTIFIED BY NEWBORN SCREENING [J].
ABMAN, SH ;
REARDON, MC ;
ACCURSO, FJ ;
HAMMOND, KB ;
SOKOL, RJ .
JOURNAL OF PEDIATRICS, 1985, 107 (06) :933-935
[2]   PERSISTENT MORBIDITY AND MORTALITY OF PROTEIN CALORIE MALNUTRITION IN YOUNG INFANTS WITH CF [J].
ABMAN, SH ;
ACCURSO, FJ ;
BOWMAN, CM .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1986, 5 (03) :393-396
[3]   HYPOALBUMINEMIA IN YOUNG INFANTS WITH CYSTIC-FIBROSIS [J].
ABMAN, SH ;
ACCURSO, FJ ;
SOKOL, RJ .
JOURNAL OF PEDIATRICS, 1990, 116 (05) :840-841
[5]  
AYALA S, 1983, ACTA PHYSIOL LAT AM, V33, P193
[6]  
CAHS R, 1969, J PEDIATR, V74, P717
[7]   PATHOLOGICAL REGULATION OF ARACHIDONIC-ACID RELEASE IN CYSTIC-FIBROSIS - THE PUTATIVE BASIC DEFECT [J].
CARLSTEDTDUKE, J ;
BRONNEGARD, M ;
STRANDVIK, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (23) :9202-9206
[8]   ABNORMAL LEVELS OF PROSTAGLANDINS AND FATTY-ACIDS IN BLOOD OF CHILDREN WITH CYSTIC-FIBROSIS [J].
CHASE, HP ;
DUPONT, J .
LANCET, 1978, 2 (8083) :236-238
[9]   EFFECTS OF ZINC-DEFICIENCY AND CASTRATION ON FATTY-ACID COMPOSITION AND DESATURATION IN RATS [J].
CLEJAN, S ;
CASTROMAGANA, M ;
COLLIPP, PJ ;
JONAS, E ;
MADDAIAH, VT .
LIPIDS, 1982, 17 (03) :129-135
[10]   RELEASE OF ESSENTIAL FATTY-ACIDS FROM THE RAT MESENTERIC VASCULAR BED PERFUSED INVITRO - MODULATION BY ZINC [J].
CUNNANE, SC ;
NASSAR, BA .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1990, 68 (07) :903-907