Hyperpigmentation in Chediak-Higashi syndrome - 29/08/11
Abstract |
We describe a 412 -year-old Saudi Arabian boy born to consanguineous parents who was initially seen with gradual onset of fever and abdominal distention. The patient was found to have speckled hypopigmentation and hyperpigmentation of the sun-exposed areas. The finding of large cytoplasmic granules in blood and bone marrow leukocytes established the diagnosis of Chediak-Higashi syndrome. We review the literature on this finding, which might be underreported, especially in darkly pigmented races.
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This supplement is made possible through an unrestricted educational grant from Stiefel Laboratories to the American Academy of Dermatology. Funding sources: None. Conflict of interest: None identified. |
Vol 49 - N° 5S
P. 244-246 - novembre 2003 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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