Diagnostic value of the café-au-lait spot in children.
نویسنده
چکیده
The significance of the cafe-au-lait spot in the diagnosis of certain disorders of childhood is still not as widely appreciated as it should be, partly due to lack of information as to the normal incidence of such pigmentation, and partly to confusion over its relation to other forms of congenital pigmentation. The varieties of congenital melanin pigmentation of the skin consist of a number of separate entities superimposed upon the basic normal colour of the skin, depending on the racial and genetic endowment of the individual. Although these entities are clear cut and separate in form and histology, and irrespective of the basic colour of the skin, a small number may give rise to difficulty in differentiation from each other. These accessory pigmented areas include the various types of moles or melanotic naevi, mongolian spots, and caf&-au-lait spots. The various types of vitiligo also merit inclusion in this group, because there is often a distinct suggestion of hyperpigmentation at the border of the depigmented areas. Although these pigmentary changes are so universally present as to be regarded as normal, under certain circumstances they may indicate the coexistence of an underlying disease. This is particularly so with respect to the cafe-au-lait spot and, to a lesser degree, to the reverse phenomenon, vitiligo. Even in a very recent and comprehensive review of the pigment cell (Riley and Fortner, 1963), the cafe-au-lait spot has been largely ignored. Early recognition of the importance of the cafe-au-lait mark was probably obscured by the nineteenth century grouping of all congenital pigmented birth marks as 'pigmented naevi', but Marie and Bernard (1896) and Chauffard (1896) independently drew attention to the association of certain types of pigmentation of the skin with generalized neurofibromatosis of the type previously described in 1882 by von Recklinghausen. Since that time the significance of these observations has been amply confirmed and extended, but the condi-
منابع مشابه
Eczematous Dermatitis Occurring on a Café-au-Lait Spot Long after Laser Radiation
A 40-year-old woman presented with an itchy erythematosquamous change of a café-au-lait spot in her face. The onset of this change occurred just after her relocation. The café-au-lait spot had been irradiated by laser approximately 20 years ago. Clinically, there was a coin-sized erythema with a slight scale on the pigmented lesion in the left lateral orbital region. Histopathologically, the le...
متن کاملRare Presentation of Neurofibromatosis and Turner Syndrome in a Pediatric Patient
Neurofibromatosis type 1 (NF1) is classically defined by the presence of multiple café-au-lait macules as one of the diagnostic criteria. Turner syndrome (TS) can also present with café-au-lait macules along with short stature. Our patient is the fifth reported with both NF1 and TS and the first who has been on growth hormone for short stature associated with TS.
متن کاملMcCune-Albright syndrome: Report of a case
A 29- year old female with bone pain and history of precocious puberty was referred for bone scintigraphy. On physical examination café au lait macular spots were noted on her neck, buttocks and left leg. Bone scan showed multiple areas of intense increased activity which was in favour of polyostotic fibrous dysplasia. Considering the presence of polyostotic fibrous...
متن کاملMccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review
McCune-Albright Syndrome (MAS) is a rare sporadic disease characterized by bone fibrous dysplasia, Café au lait spots and a variable association of hyperfunction endocrine disorders. There is not any certain treatment available for this syndrome, and both physical and emotional disability in these patients is still a major concern for physicians. In present report we have described a 10- year-o...
متن کاملBloom’s syndrome: A case presentation
Bloom’s syndrome (BS) is a rare, autosomal recessive disease characterized by short stature, erythematous skin lesions with photosensitivity, hypo- and hyperpigmentation and recurrent bacterial infections due to immune deficiency. We report a 13-year old girl with erythema and telangiectasia in butterfly distribution on face, photosensitivity, multiple café au lait spots on trunk and extremitie...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Archives of disease in childhood
دوره 41 217 شماره
صفحات -
تاریخ انتشار 1966