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1.
JPAD-Journal of Pakistan Association of Dermatologists. 2015; 25 (4): 322-326
in English | IMEMR | ID: emr-181152

ABSTRACT

Angiolymphoid hyperplasia with eosinophilia [AHE] has an unknown pathogenesis but is considered a reactive phenomenon, possibly in response to or in association with an underlying vascular malformation. There is history of trauma in some cases, and hyperestrogenemia [e.g. pregnancy, oral contraceptive use] may foster lesion growth. T-cell monoclonality has been reported in few cases. We report such a case in a 39-year-old male who visited our hospital with multiple nodules on the occipital of his head.

2.
JPAD-Journal of Pakistan Association of Dermatologists. 2014; 24 (4): 351-354
in English | IMEMR | ID: emr-162421

ABSTRACT

Silvery hair and severe dysfunction of the central nervous system [Neuroectodermal melanolysosomal disease or Elejalde Syndrome] characterize this rare autosomal recessive syndrome. Main clinical features include silver-leaden hair, bronze skin after sun exposure, and neurologic involvement. Large granules of melanin unevenly distributed in the hair shaft are observed. Abnormal melanocytes and melanosomes and abnormal inclusion bodies in fibroblasts may be present. We report a 10-year-old girl with a silver-leaden [silvery] hair, bronze skin color on sun-exposed areas, generalized hypopigmentation of covered body parts and congenital seizures. The child was the elder of two children born of a consanguineous marriage. The younger sibling, a female neonate, had same clinical presentation

3.
JPAD-Journal of Pakistan Association of Dermatologists. 2014; 24 (1): 101-102
in English | IMEMR | ID: emr-157653
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