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عنوان
An unusual presentation of seborrheic keratoses in a man with hereditary hemochromatosis

پدید آورنده
Loh, Tiffany Y; Cohen, Philip R,Loh, Tiffany Y; Cohen, Philip R

موضوع

رده

کتابخانه
کتابخانه مطالعات اسلامی به زبان های اروپایی

محل استقرار
استان: قم ـ شهر: قم

کتابخانه مطالعات اسلامی به زبان های اروپایی

تماس با کتابخانه : 32910706-025

LA0xn124r8

انگلیسی

An unusual presentation of seborrheic keratoses in a man with hereditary hemochromatosis
[Article]
Loh, Tiffany Y; Cohen, Philip R

Hereditary hemochromatosis is an autosomalrecessive disorder that disturbs iron metabolismand results in iron deposition throughout the body.Iron accumulation in various organs may cause awide range of systemic symptoms and cutaneousmanifestations of the disease are particularlystriking. Classically, hereditary hemochromatosis hasbeen termed "bronze diabetes." Although diffusehyperpigmentation is a well-described feature ofthis disease, other cutaneous symptoms may alsooccur, and a variety of anomalies may be observed.We present a case of long-standing hereditaryhemochromatosis associated with hypopigmentedplaques, which were found to be seborrheic keratoseson histologic examination. The cutaneous findingsin hereditary hemochromatosis are summarized andan unusual case of seborrheic keratosis manifestingas hypopigmented plaques in a man with hereditaryhemochromatosis is described. PubMed was usedto search the following terms: hemochromatosis,hereditary, hyperpigmentation, hypopigmentation,keratosis, melanin, seborrheic, siderosis. Despitethe generalized hyperpigmentation that is usuallyobserved in hereditary hemochromatosis, seborrheickeratosis may present rarely as hypopigmented lesionsin individuals affected by this disease. Therefore,seborrheic keratoses should be considered in thedifferential diagnosis in hemochromatosis patientswho present with uncharacteristic pigmentation

2017
Dermatology Online Journal
23/4

Loh, Tiffany Y; Cohen, Philip R

 مطالعه متن کتاب 

[Article]
275578

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الاقتراح / اعلان الخلل

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تتم إدارة هذا الموقع عبر مؤسسة دار الحديث العلمية - الثقافية ومركز البحوث الكمبيوترية للعلوم الإسلامية (نور)
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