Chronic mucocutaneous candidosis associated with hypothyroidism: A distinct syndrome?

被引:32
作者
Coleman, R [1 ]
Hay, RJ [1 ]
机构
[1] GUYS HOSP, ST JOHNS INST DERMATOL, LONDON SE1 9RT, ENGLAND
关键词
D O I
10.1111/j.1365-2133.1997.tb08741.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Chronic mucocutaneous candidosis (CMC) is a rare, complex disorder characterized by chronic and recurrent candida infections of the skin, nails and oropharynx. In over 50% of cases there is an associated endocrine disease, the complex being described as the candida endocrinopathy syndrome. Inheritance of familial endocrine associated cases has been thought to follow an autosomal recessive pattern. In addition, autosomal recessive and autosomal dominant forms of CMC not associated with endocrinopathy hare been described, We report a new syndrome in which there is vertical transmission of CMC within families associated with primary hypothyroidism. This suggests that the candida endocrinopathy syndrome can be subdivided into at least two types, one associated with hypoparathyroidism and/or hypoadrenalism which is inherited as an autosomal recessive trait, the other associated with hypothyroidism which is an autosomal dominant disease. We emphasize the importance of early and regular monitoring thyroid function in individuals with CMC and a need to provide appropriate genetic counselling to affected members.
引用
收藏
页码:24 / 29
页数:6
相关论文
共 20 条
[1]   CLINICAL VARIATION OF AUTOIMMUNE POLYENDOCRINOPATHY CANDIDIASIS ECTODERMAL DYSTROPHY (APECED) IN A SERIES OF 68 PATIENTS [J].
AHONEN, P ;
MYLLARNIEMI, S ;
SIPILA, I ;
PERHEENTUPA, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (26) :1829-1836
[2]  
BLIZZARD RM, 1968, PEDIATRICS, V42, P231
[3]  
CHIPPS BE, 1979, JOHNS HOPKINS MED J, V144, P175
[4]   CLINICAL PERSPECTIVE, IMMUNE DEFENSE-MECHANISMS, AND CURRENT CONCEPTS OF THERAPY [J].
EDWARDS, JE ;
LEHRER, RI ;
STIEHM, ER ;
FISCHER, TJ ;
YOUNG, LS .
ANNALS OF INTERNAL MEDICINE, 1978, 89 (01) :91-106
[5]   HLA TYPE AND OCCURRENCE OF DISEASE IN FAMILIAL POLYGLANDULAR FAILURE [J].
EISENBARTH, G ;
WILSON, P ;
WARD, F ;
LEBOVITZ, HE .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (02) :92-94
[6]   CHRONIC MUCOCUTANEOUS CANDIDIASIS IN CHILDHOOD AND COMPLICATIONS OF NON-CANDIDA INFECTION - A REPORT OF THE PEDIATRIC IMMUNODEFICIENCY COLLABORATIVE STUDY-GROUP [J].
HERROD, HG .
JOURNAL OF PEDIATRICS, 1990, 116 (03) :377-382
[7]  
Higgs J M, 1973, Guys Hosp Rep, V122, P135
[8]   MEASUREMENT OF FE-59 ABSORPTION AND RETENTION IN PATIENTS WITH FAMILIAL CHRONIC MUCO-CUTANEOUS CANDIDIASIS USING METHOD OF WHOLE-BODY COUNTING [J].
HIGGS, JM ;
SMITH, P ;
SMITH, T .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 1976, 1 (04) :369-376
[9]   CHRONIC MUCO-CUTANEOUS CANDIDIASIS - ASSOCIATED ABNORMALITIES OF IRON METABOLISM [J].
HIGGS, JM ;
WELLS, RS .
BRITISH JOURNAL OF DERMATOLOGY, 1972, 86 :88-&
[10]   CHRONIC MUCOCUTANEOUS CANDIDIASIS [J].
KIRKPATRICK, CH .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1994, 31 (03) :S14-S17